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TANAKA Tomonori
University Hospital / Diagnostic Pathology
Assistant Professor

Researcher basic information

■ Research Keyword
  • Pathology
  • Diffuse parenchymal lung disease
  • Non-neoplastic lung disease
  • Interstitial pneumonia
■ Research Areas
  • Life sciences / Human pathology / Pulmonary pathology

Research activity information

■ Paper
  • Taiki Fukuda, Kaori Ishida, Tomonori Tanaka, Kensuke Kataoka, Reoto Takei, Yuki Ko, Yusei Nakamura, Mikiko Hashisako, Hiromitsu Sumikawa, Ryoko Egashira, Junya Tominaga, Hiroya Ojiri, Hiroto Hatabu, Tomoki Kimura, Yasuhiro Kondoh, Junya Fukuoka, Takeshi Johkoh
    BACKGROUND: Interstitial lung abnormalities (ILA) are CT-detected interstitial abnormalities that may represent early-stage interstitial lung disease (ILD). However, histopathologic correlations remain limited, with previous studies reporting conflicting results. In 2025, the American Thoracic Society (ATS) established criteria defining the boundary between ILA and ILD. This study aimed to investigate the histopathological spectrum of Fleischner-defined ILA, correlate findings with CT features and outcomes, and reclassify cases according to 2025 ATS criteria. METHODS: This retrospective study analyzed 30 consecutive patients who underwent surgical lung biopsy between January 2010 and December 2021. All cases had ILA per Fleischner Society criteria and were reclassified using 2025 ATS criteria. Three pulmonary pathologists evaluated dominant and co-existing histopathological patterns. Two chest radiologists independently assessed CT findings. Overall survival was compared between usual interstitial pneumonia (UIP)-related and non-UIP-related groups using Kaplan-Meier analysis. RESULTS: Twenty patients (66.7 %) were men; mean age was 63.6 ± 6.5 years; 27 (90 %) had fibrotic ILA. The most common dominant pattern was UIP (43.3 %), followed by nonspecific interstitial pneumonia (NSIP) and bronchiolocentric interstitial pneumonia (BIP) (20 % each). Overall, 96.7 % of cases met 2025 ATS criteria for ILD (subclinical ILD). On CT, all UIP and NSIP cases showed reticular opacity and traction bronchiectasis, while BIP typically exhibited branching linear opacities. During median follow-up of 92.1 months, overall survival did not differ significantly between UIP-related and non-UIP-related groups (p = 0.595). CONCLUSIONS: This study of Fleischner-defined ILA, predominantly reclassified as subclinical ILD by 2025 ATS criteria, demonstrates diverse histopathological patterns beyond UIP, including BIP, highlighting pathological heterogeneity.
    Jan. 2026, Respiratory investigation, 64(2) (2), 101374 - 101374, English, International magazine
    Scientific journal

  • Taiki Fukuda, Yasuhiko Yamano, Kaori Ishida, Tomonori Tanaka, Ryoko Egashira, Hiromitsu Sumikawa, Mikiko Hashisako, Junya Tominaga, Mai Matsumura, Midori Ueno, Daisuke Yamada, Yuki Ko, Yusei Nakamura, Hiroya Ojiri, Hiroto Hatabu, Reoto Takei, Kensuke Kataoka, Tomoki Kimura, Yasuhiro Kondoh, Junya Fukuoka, Takeshi Johkoh
    PURPOSE: To perform comprehensive radiological-pathological correlation in systemic sclerosis-associated interstitial lung disease (SSc-ILD) and identify characteristic findings, including subtle abnormalities potentially representing early-stage CT findings. MATERIAL AND METHODS: This retrospective study included 28 SSc-ILD patients who underwent surgical lung biopsy between July 2008 and July 2018. Two chest radiologists independently reviewed whole-lung high-resolution CT (HRCT) images, with the other two radiologists evaluating biopsy sites. Faint amorphous nodular opacity (FANO) was defined as a small, faint nodular opacity superimposed on amorphous ground-glass opacity (GGO) within 1 cm of the pleural surface, showing a band-like distribution parallel to the pleura. Three pulmonary pathologists performed histological evaluation. Discrepancies were resolved through consensus, with CT-pathologic correlation established through joint radiologist-pathologist review. RESULTS: Twenty-eight patients (mean age, 57 years ± 10; 15 men) were evaluated with 79 biopsy specimens. Nonspecific interstitial pneumonia was the predominant pattern on whole-lung HRCT (21 patients, 75%) and pathology (17 patients, 61%). At biopsy sites, GGO was most frequent (92%), followed by reticulation (84%). Reticulation was accompanied by GGO in nearly all cases, reflecting underlying diffuse fibrotic changes. Reticulation patterns with or without traction bronchiolectasis corresponded to varying fibrosis types, spatial distribution, and architectural destruction severity. Specifically, irregular reticulation with traction bronchiolectasis indicated dense fibrosis with severe destruction, representing UIP-like features. FANO was observed in 18 patients (64%), predominantly in anterolateral upper lobes, and corresponded pathologically to perivenular fibrosis and peribronchiolar metaplasia with or without mucostasis. Longitudinal evaluation (median 32.5 months) in 14 patients showed progression in 71%; half of these showed coalescence into subpleural curvilinear opacities with reticulation. CONCLUSION: SSc-ILD demonstrates predominantly diffuse fibrotic changes. Irregular reticulation with traction bronchiolectasis indicates UIP-like features, potentially identifying patients at risk for progression. FANO, observed most commonly in anterolateral upper lobes, frequently progresses to reticulation on longitudinal follow-up, suggesting potential value for early-stage detection. SSc-ILD demonstrated diffuse fibrotic changes as a characteristic feature, while irregular reticulation with traction bronchiolectasis indicated UIP-like fibrosis with severe architectural destruction. FANO, a newly described finding observed in 64% of cases, was predominantly in anterolateral upper lobes and corresponded to perivenular fibrosis and peribronchiolar metaplasia, representing potential early-stage changes.
    Dec. 2025, Japanese journal of radiology, English, Domestic magazine
    Scientific journal

  • Takashi Ogura, Taiki Furukawa, Yasuhiro Kondoh, Tomonori Tanaka, Yukio Kashima, Motoyasu Kato, Tsukasa Okamoto, Haruyuki Ishii, Takeshi Jokoh, Ryoko Egashira, Junya Fukuoka, Hironao Hozumi, Ryo Teramachi, Takafumi Suda, Toru Arai, Yoshiaki Zaizen, Atsushi Miyamoto, Keisuke Tomii, Kiminori Fujimoto, Tae Iwasawa, Chikatoshi Sugimoto, Yasuhiro Terasaki, Noriyuki Enomoto, Hiroaki Sugiura, Mishie Tanino, Kazuhiro Tabata, Fumikazu Sakai, Akira Hebisawa, Tamiko Takemura, Hiromitsu Sumikawa, Hideya Kitamura, Yutaro Nakamura, Shinobu Kunugi, Kazuto Ashizawa, Mikiko Hashisako, Yuko Nishimoto, Hidetake Yabuuchi, Masashi Kitani, Shinyu Izumi, Yasuyuki Kurihara, Kiyoshi Murata, Junya Tominaga, Takahiko Kasai, Kaori Ishida, Kyoko Otani, Naoko Takeuchi, Makoto Ishii
    European Respiratory Society, Sep. 2025, Idiopathic interstitial pneumonias, PA5069 - PA5069
    International conference proceedings

  • Kurumi Seki, Jijgee Munkhdelger, Andrey Bychkov, Tomonori Tanaka, Shinobu Kunugi, Ryoko Saito-Koyama, Yukio Kashima, Yoshiaki Zaizen, Koji Okudela, Kensuke Kataoka, Yasuhiko Yamano, Yasuhiro Kondoh, Takeshi Johkoh, Junya Fukuoka
    BACKGROUND: The interobserver agreement regarding airway-centered fibrosis (ACF), the key diagnostic feature of fibrotic hypersensitivity pneumonitis (fHP) has not been sufficiently addressed to date. We applied digital image analysis to investigate this issue and extracted histological features of ACF to correlate with fHP diagnosis. METHODS: A total of 111 selected glass slides from 17 fHP and 30 idiopathic pulmonary fibrosis (IPF) were scanned and seven expert pulmonary pathologists were tasked with digital annotation of ACF. Interobserver agreement on annotated ACF was assessed using Fleiss' kappa value. ACF recognized by majority of pathologists (4 or more) were considered as consensus ACF (cACF), and their frequencies were compared between fHP and IPF cases. RESULTS: Fleiss' kappa agreement in ACF recognition was 0.32 among seven pathologists. A significant difference between cryobiopsy and VATS specimens regarding an average ACF count per slide (p = 0.012) was found. The number of cACFs in a single case ranged from 0 to 20 (mean 5.71) for fHP cases and 0 to 13 (mean 1.80) for IPF cases (p = 0.011). When limited to surgical biopsies, the average number of cACF was 10.3 for fHP vs. 1.68 for IPF (p < 0.001). The common characteristic features of cACF in fHP were their confinement to the vicinity of respiratory bronchioles, frequent association with peribronchiolar metaplasia, and mild to moderate lymphocytic infiltration. CONCLUSIONS: The recognition of ACF varies widely among pathologists. We identified common histologic features of ACF in fHP cases, proposing criteria for ACF recognition in fHP.
    May 2025, Respiratory investigation, 63(3) (3), 314 - 321, English, International magazine
    [Refereed]
    Scientific journal

  • Rena Uno, Yoh Zen, Tomonori Tanaka, Hirochika Toyama, Takumi Fukumoto, Keitaro Sofue, Tomoo Itoh
    ABSTRACT We present a case of pancreatic ductal carcinoma with a microcystic appearance. A 64‐year‐old woman was found to have a pancreatic mass during a routine medical checkup. The tumor was well‐circumscribed and multicystic; thus, she was followed up for suspected serous cystadenoma. However, the tumor gradually enlarged in the following 2.5 years; subsequently, she underwent a Whipple procedure. Grossly, the cut surface of the tumor was honeycomb‐like with small cysts. Histologically, the cysts were ductal structures lined by a relatively bland, cuboidal or columnar epithelium with mildly enlarged nuclei. No intracytoplasmic mucus was observed. The presence of stromal invasion confirmed the diagnosis of ductal carcinoma. KRAS was wild type. Postoperative course was uneventful, with no recurrence to date (followup period: 5.5 years postsurgery). The present case did not meet any known subtypes of pancreatic ductal carcinoma. The tumor resembled a large duct variant, which typically shows a microcystic appearance. However, unlike the present case, the large duct type usually consists of mucus‐rich neoplastic cells. A recent study on cholangiocarcinoma proposed a novel tubulocystic subtype characterized by microcystic neoplastic glands and adenofibromatous stroma, which is morphologically similar to the present case. The present case may correspond to a pancreatic counterpart of tubulocystic cholangiocarcinoma.
    Wiley, Apr. 2025, Pathology International, 75(5) (5), 243 - 246
    [Refereed]
    Scientific journal

  • 財前 圭晃, 寺崎 泰弘, 蛇澤 晶, 石田 佳央理, 橋迫 美貴子, 松村 舞依, 木谷 匡志, 功刀 しのぶ, 田中 伴典, 田畑 和宏, 澤住 知枝, 奥寺 康司, 武村 民子, 福岡 順也
    (一社)日本呼吸器学会, Mar. 2025, 日本呼吸器学会誌, 14(増刊) (増刊), 199 - 199, Japanese

  • Ryo Hara, Satoshi Watanabe, Nanao Terada, Kazumasa Kase, Atsushi Muto, Yasuhito Hamaguchi, Takashi Matsushita, Hiroko Ikeda, Tomonori Tanaka, Seiji Yano
    Dec. 2024, Rheumatology (Oxford, England), 63(12) (12), e336-e338, English, International magazine
    [Refereed]
    Scientific journal

  • Takahiro Tsuchiya, Keiichiro Uehara, Tomonori Tanaka, Yasuyoshi Okamura, Chisato Ohe, Kenichi Kohashi, Tomoo Itoh
    Springer Science and Business Media LLC, Oct. 2024, Cureus
    [Refereed]
    Scientific journal

  • Hiromitsu Sumikawa, Takeshi Johkoh, Ryoko Egashira, Hiroaki Sugiura, Chikatoshi Sugimoto, Tomonori Tanaka, Masahisa Nakamura, Akihiro Kuriu, Noriyuki Tomiyama, Tomoyuki Fujisawa, Yutaro Nakamura, Takafumi Suda
    BACKGROUND: Usual interstitial pneumonia (UIP) cases without honeycombing (possible UIP) included various CT features and was often difficult to diagnose. PURPOSE: This study aimed to classify the cases with possible UIP on CT features using cluster analysis and evaluate the features of subsets of participants and the correlation of prognosis. MATERIALS AND METHODS: The study included 85 patients with possible UIP in the 2011 idiopathic pulmonary fibrosis (IPF) guideline with radiological diagnosis. All cases underwent surgical biopsies and were diagnosed by multidisciplinary discussion (MDD) from the nationwide registry in Japan. The readers evaluated pulmonary opacity, nodules, cysts, and predominant distribution which were reclassified by IPF guidelines in 2018. Additionally, cases were classified into four groups by cluster analysis based on CT findings. The differences in survival among IPF classification and the clusters were evaluated. RESULTS: Cases were diagnosed as IPF (n = 55), NSIP (n = 4), unclassifiable (n = 23), and others (n = 3) by MDD. Cluster analysis revealed 4 clusters by CT features (n = 47, 16, 19 and 3, respectively). Cluster 1 had fewer lesions overall. Cluster 2 have many pure ground-glass opacities and ground-glass opacities with reticulation. Cluster 3 had many reticular opacities and nodules with few lower predominant distributions. Cluster 4 was characterized by peribronchovascular consolidation.The mean survival time of cluster 1 (4518 days) was significantly better than cluster 2, 3, and 4 (1843, 2196, and 1814 days, respectively) (p = 0.03). CONCLUSION: In conclusion, UIP without honeycombing included various CT patterns and MDD diagnoses. Significangly differences in prognosis were observed among clusters classified by CT findings.
    Jul. 2024, European journal of radiology, 179, 111651 - 111651, English, International magazine
    [Refereed]
    Scientific journal

  • Naoto Shirakami, Shingo Kanaji, Atsushi Shimada, Tomosuke Mukoyama, Ryuichiro Sawada, Hitoshi Harada, Tomonori Tanaka, Naoki Urakawa, Hironobu Goto, Hiroshi Hasegawa, Kimihiro Yamashita, Takeru Matsuda, Yoshihiro Kakeji
    Abstract Background Herein, we report a case of gastric antrum cancer with multiple invasions to other organs that was completely cured with laparoscopic distal gastrectomy after preoperative chemotherapy in a patient with poor general condition. Case presentation An 80-year-old male patient was diagnosed with anemia during follow-up for cerebral lacunar infarction at another hospital. He was diagnosed with advanced-stage gastric antrum cancer and was referred to our hospital. On esophagogastroduodenoscopy, type 2 advanced-stage gastric cancer was detected at the greater curvature of the antrum, and the biopsy results revealed tubular adenocarcinoma. Contrast-enhanced computed tomography scan revealed multiple invasions to other organs, thick gastric wall with contrast effect, and superior mesenteric vein tumor thrombus. However, there was no evidence of distant metastasis on positron emission tomography/computed tomography scan. The clinical diagnosis was stage IVA gastric cancer. Pancreatoduodenectomy with portal vein resection could be important at this point. However, preoperative chemotherapy with S-1 and oxaliplatin was administered instead of performing extended surgery because the patient had poor general condition (performance status score of 3). The patient received three cycles of preoperative chemotherapy at the hospital along with rehabilitation and nutritional management with oral nutritional supplements. After treatment, the performance status score of the patient improved from 3 to 1. Furthermore, in terms of clinical therapeutic effect, the patient achieved partial response. Hence, laparoscopic distal gastrectomy with D2 lymph node dissection and partial transverse colectomy was performed. After surgery, the patient was admitted for oral intake on postoperative day 6 and was discharged on postoperative day 21. Based on the histopathological examination, gastric cancer had disappeared, and there were no evident malignant findings. Therefore, gastric cancer was classified as grade 3 according to the histological treatment efficacy criteria. The patient did not present with recurrence at 2 years after surgery. Conclusions By actively administering preoperative chemotherapy, minimally invasive radical surgery with maximum preservation of the surrounding organs can be performed for locally far advanced-stage gastric cancer in older patients with poor general condition.
    Springer Science and Business Media LLC, Jun. 2024, Surgical Case Reports, 10(1) (1)
    [Refereed]
    Scientific journal
    Link to Kobe Univ. Repository (Kernel)

  • Midori Ueno, Ryoko Egashira, Mikiko Hashisako, Kiminori Fujimoto, Taiki Fukuda, Yoshiko Hayashida, Hiromitsu Sumikawa, Junya Tominaga, Tomonori Tanaka, Yasuhiro Terasaki, Junya Fukuoka, Yasuhiko Nishioka, Takatoshi Aoki, Toshifumi Gabata, Hiroto Hatabu, Takeshi Johkoh
    BACKGROUND AND PURPOSE: Idiopathic dendriform pulmonary ossification (DPO) is mostly asymptomatic, and detected incidentally in lung CT. There have been no reports on the precise CT-pathologic correlation and the prevalence of idiopathic DPO. This study aimed to clarify the histological background and prevalence of idiopathic DPO. MATERIALS AND METHODS: Sixteen patients with histologically confirmed idiopathic DPO (12 men and 4 women; mean age, 38.8 years; range 22-56 years) were identified in a nationwide epidemiological survey. Local HRCT findings of pre-biopsy examinations, such as branching, round, linear structures with or without high attenuation were compared side by side with histological findings. The attenuation of branching, round, and linear structures was classified into three-point levels on bone window images (width, 2500 HU; level, 500 HU). Furthermore, we collected continuous pulmonary CT images of 8111 cases for checking up metastasis from extrathoracic malignancy at a single institution, and evaluated the prevalence of interstitial lung abnormalities (ILAs) and DPO. RESULTS: In all 16 cases, branching (n = 15, 93%), round (n = 5, 31%), or linear (n = 5, 31%) structures were identified, histologically corresponding to dendriform ossification and cicatricial organizing pneumonia (OP)/fibrosis. Histologically, ossification was confirmed in all the 16 patients. However, in two cases, a highly attenuated structure could not be detected on the pre-biopsy CT of the same area. Regarding the prevalence of idiopathic DPO, 283 (3.5%) of 8111 patients had ILAs, of which a total of 26 (0.3% of all cases, 9.2% of ILAs cases) had DPO. CONCLUSION: Idiopathic DPO showed linear or branching structures with or without high attenuation on CT, corresponded to ossification, cicatricial OP/fibrosis. DPO was seen in 9.2% of ILAs cases. Idiopathic DPO is one of pathologic phenotypes of ILAs.
    May 2024, Japanese journal of radiology, English, Domestic magazine
    [Refereed]
    Scientific journal

  • 西山 理, 山崎 亮, 御勢 久也, 吉川 和也, 松本 久子, 田中 伴典, 澄川 裕充, 穂積 宏尚, 藤澤 朋幸, 須田 隆文
    (一社)日本呼吸器学会, Mar. 2024, 日本呼吸器学会誌, 13(増刊) (増刊), 365 - 365, Japanese

  • Hisao Sano, Ethan N. Okoshi, Yuri Tachibana, Tomonori Tanaka, Kris Lami, Wataru Uegami, Yoshio Ohta, Luka Brcic, Andrey Bychkov, Junya Fukuoka
    Background: When obtaining specimens from pulmonary nodules in TBLB, distinguishing between benign samples and mis-sampling from a tumor presents a challenge. Our objective is to develop a machine-learning-based classifier for TBLB specimens. Methods: Three pathologists assessed six pathological findings, including interface bronchitis/bronchiolitis (IB/B), plasma cell infiltration (PLC), eosinophil infiltration (Eo), lymphoid aggregation (Ly), fibroelastosis (FE), and organizing pneumonia (OP), as potential histologic markers to distinguish between benign and malignant conditions. A total of 251 TBLB cases with defined benign and malignant outcomes based on clinical follow-up were collected and a gradient-boosted decision-tree-based machine learning model (XGBoost) was trained and tested on randomly split training and test sets. Results: Five pathological changes showed independent, mild-to-moderate associations (AUC ranging from 0.58 to 0.75) with benign conditions, with IB/B being the strongest predictor. On the other hand, FE emerged to be the sole indicator of malignant conditions with a mild association (AUC = 0.66). Our model was trained on 200 cases and tested on 51 cases, achieving an AUC of 0.78 for the binary classification of benign vs. malignant on the test set. Conclusion: The machine-learning model developed has the potential to distinguish between benign and malignant conditions in TBLB samples excluding the presence or absence of tumor cells, thereby improving diagnostic accuracy and reducing the burden of repeated sampling procedures for patients.
    MDPI AG, Feb. 2024, Cancers, 16(4) (4), 731 - 731
    [Refereed]
    Scientific journal

  • Hiromichi Iwashita, Yoshinori Kawabata, Hiroyuki Hayashi, Shoichiro Matsushita, Tsuneo Yamashiro, Mai Matsumura, Yukihiro Yoshimura, Toshiaki Kataoka, Hideaki Mitsui, Takehisa Suzuki, Toshihiro Misumi, Tomonori Tanaka, Sosuke Ishijima, Junya Fukuoka, Tae Iwasawa, Takashi Ogura, Koji Okudela
    Abstract Risk factors of severe coronavirus disease 2019 (COVID-19) have been previously reported; however, histological risk factors have not been defined thus far. The aim of this study was to clarify subclinical hidden interstitial lung disease (ILD) as a risk factor of severe pneumonia associated with COVID-19. We carefully examined autopsied lungs and chest computed tomography scanning (CT) images from patients with COVID-19 for interstitial lesions and then analyzed their relationship with disease severity. Among the autopsy series, subclinical ILD was found in 13/27 cases (48%) in the COVID-19 group, and in contrast, 8/65 (12%) in the control autopsy group (p = 0.0006; Fisher’s exact test). We reviewed CT images from the COVID-19 autopsy cases and verified that subclinical ILD was histologically detectable in the CT images. Then, we retrospectively examined CT images from another series of COVID-19 cases in the Yokohama, Japan area between February–August 2020 for interstitial lesions and analyzed the relationship to the severity of COVID-19 pneumonia. Interstitial lesion was more frequently found in the group with the moderate II/severe disease than in the moderate I/mild disease (severity was evaluated according to the COVID-19 severity classification system of the Ministry of Health, Labor, and Welfare [Japan]) (moderate II/severe, 11/15, 73.3% versus moderate I/mild, 108/245, 44.1%; Fisher exact test, p = 0.0333). In conclusion, it was suggested that subclinical ILD could be an important risk factor for severe COVID-19 pneumonia. A benefit of these findings could be the development of a risk assessment system using high resolution CT images for fatal COVID-19 pneumonia.
    Springer Science and Business Media LLC, Oct. 2023, BMC Pulmonary Medicine, 23(1) (1), English
    [Refereed]
    Scientific journal

  • Kris Lami, Noriaki Ota, Shinsuke Yamaoka, Andrey Bychkov, Keitaro Matsumoto, Wataru Uegami, Jijgee Munkhdelger, Kurumi Seki, Odsuren Sukhbaatar, Richard Attanoos, Sabina Berezowska, Luka Brcic, Alberto Cavazza, John C. English, Alexandre Todorovic Fabro, Kaori Ishida, Yukio Kashima, Yuka Kitamura, Brandon T. Larsen, Alberto M. Marchevsky, Takuro Miyazaki, Shimpei Morimoto, Mutsumi Ozasa, Anja C. Roden, Frank Schneider, Maxwell L. Smith, Kazuhiro Tabata, Angela M. Takano, Tomonori Tanaka, Tomoshi Tsuchiya, Takeshi Nagayasu, Hidenori Sakanashi, Junya Fukuoka
    Elsevier BV, Aug. 2023, The American Journal of Pathology
    [Refereed]
    Scientific journal

  • Ayano Tanigawa, Takeshi Fukumoto, Shinya Imamura, Korefumi Nakamura, Tomonori Tanaka, Tomoo Itoh, Eiji Nakano, Chikako Nishigori, Akiharu Kubo
    Wiley, Feb. 2023, The Journal of Dermatology, 50(7) (7)
    [Refereed]
    Scientific journal

  • Atsuhiko Yatani, Naoko Katsurada, Takafumi Fukui, Jun Yamada, Hiroki Satoh, Chihiro Mimura, Daisuke Hazama, Masatsugu Yamamoto, Naoe Jimbo, Tomonori Tanaka, Motoko Tachihara
    Ultrathin bronchoscopy has been reported to have a higher diagnostic yield than thin bronchoscopy for small peripheral lung lesions in transbronchial biopsy under radial endobronchial ultrasonography (EBUS). However, data comparing the number of tumor cells in non-small cell lung cancer (NSCLC) are limited. We retrospectively compared the number of NSCLC tumor cells in peripheral lung lesions obtained using an ultrathin bronchoscope and a thin bronchoscope with radial EBUS between April 2020 and October 2021. In all patients, we used virtual bronchoscopic navigation (VBN) software, and guide sheaths were used in thin bronchoscopy cases. A total of 175 patients were enrolled in this study. Ultrathin bronchoscopy cases (n = 69) had lesions with a smaller diameter that are more peripherally located compared to thin bronchoscopy cases (n = 106) (median, 25.0 vs. 26.5 mm, mean bronchial generations accessed by bronchoscopy; 4.4±1.2 vs. 3.8±1.0, respectively; p<0.010). There were no significant differences in the overall diagnostic yield (ultrathin vs. thin bronchoscopy cases, 68.1% vs. 72.6%, p = 0.610) or diagnostic yield in only lung cancer cases (78.6% vs. 78.5%, p = 1.000). In histologically NSCLC cases (n = 102), the maximum number of tumor cells per slide as the primary endpoint was similar (average, 307.6±246.7 vs. 328.7±314.9, p = 0.710). The success rate of the Oncomine™ analysis did not differ significantly (80.0% vs. 55.6%, p = 0.247). The yield of NSCLC tumor cells was not different between the samples obtained by the ultrathin bronchoscope and those obtained by the thin bronchoscope.
    2023, PloS one, 18(8) (8), e0290609, English, International magazine
    [Refereed]
    Scientific journal
    Link to Kobe Univ. Repository (Kernel)

  • Kris Lami, Andrey Bychkov, Keitaro Matsumoto, Richard Attanoos, Sabina Berezowska, Luka Brcic, Alberto Cavazza, John C. English, Alexandre Todorovic Fabro, Kaori Ishida, Yukio Kashima, Brandon T. Larsen, Alberto M. Marchevsky, Takuro Miyazaki, Shimpei Morimoto, Anja C. Roden, Frank Schneider, Mano Soshi, Maxwell L. Smith, Kazuhiro Tabata, Angela M. Takano, Kei Tanaka, Tomonori Tanaka, Tomoshi Tsuchiya, Takeshi Nagayasu, Junya Fukuoka
    Context.— The accurate identification of different lung adenocarcinoma histologic subtypes is important for determining prognosis but can be challenging because of overlaps in the diagnostic features, leading to considerable interobserver variability. Objective.— To provide an overview of the diagnostic agreement for lung adenocarcinoma subtypes among pathologists and to create a ground truth using the clustering approach for downstream computational applications. Design.— Three sets of lung adenocarcinoma histologic images with different evaluation levels (small patches, areas with relatively uniform histology, and whole slide images) were reviewed by 18 international expert lung pathologists. Each image was classified into one or several lung adenocarcinoma subtypes. Results.— Among the 4702 patches of the first set, 1742 (37%) had an overall consensus among all pathologists. The overall Fleiss κ score for the agreement of all subtypes was 0.58. Using cluster analysis, pathologists were hierarchically grouped into 2 clusters, with κ scores of 0.588 and 0.563 in clusters 1 and 2, respectively. Similar results were obtained for the second and third sets, with fair-to-moderate agreements. Patches from the first 2 sets that obtained the consensus of the 18 pathologists were retrieved to form consensus patches and were regarded as the ground truth of lung adenocarcinoma subtypes. Conclusions.— Our observations highlight discrepancies among experts when assessing lung adenocarcinoma subtypes. However, a subsequent number of consensus patches could be retrieved from each cluster, which can be used as ground truth for the downstream computational pathology applications, with minimal influence from interobserver variability.
    Archives of Pathology and Laboratory Medicine, Nov. 2022, Archives of Pathology & Laboratory Medicine, English, International magazine
    [Refereed]
    Scientific journal

  • Naoko Katsurada, Motoko Tachihara, Naoe Jimbo, Masatsugu Yamamoto, Junya Yoshioka, Chihiro Mimura, Hiroki Satoh, Koichi Furukawa, Takehiro Otoshi, Tatsunori Kiriu, Yuichiro Yasuda, Tomonori Tanaka, Tatsuya Nagano, Yoshihiro Nishimura
    Background Adequate tumor tissue is required to make the best treatment choice for non-small cell lung cancer (NSCLC). Transbronchial biopsy (TBB) by endobronchial ultrasonography with a guide sheath (EBUS-GS) is useful to diagnose peripheral lung lesions. The data of tumor cell numbers obtained by two different sizes of GSs is limited. We conducted this study to investigate the utility of a large GS kit to obtain many tumor cells in patients with NSCLC. Methods Patients with a peripheral lung lesion and suspected of NSCLC were prospectively enrolled. They underwent TBB with a 5.9-mm diameter bronchoscope with a large GS. When the lesion was invisible in EBUS, we changed to a thinner bronchoscope and TBB was performed with a small GS. We compared the tumor cell number prospectively obtained with a large GS (prospective large GS group) and those previously obtained with a small GS (small GS cohort). The primary endpoint was the tumor cell number per sample, and we assessed characteristics of lesions that could be obtained by TBB with large GS. Results Biopsy with large GS was performed in 55 of 87 patients (63.2%), and 37 were diagnosed with NSCLC based on histological samples. The number of tumor cells per sample was not different between two groups (658±553 vs. 532±526, estimated difference between two groups with 95% confidence interval (CI); 125 (-125–376), p = 0.32). The sample size of the large GS group was significantly larger than that of the small GS cohort (1.75 mm2 vs. 0.83 mm2, estimated difference with 95% CI; 0.92 (0.60–1.23) mm2, p = 0.00000019). The lesion involving a third or less bronchus generation was predictive factors using large GS. Conclusions The sample size obtained with large GS was significantly larger compared to that obtained with small GS, but there was no significant difference in tumor cell number. The 5.9-mm diameter bronchoscope with large GS can be used for lesions involving a third or less bronchus generation.
    Public Library of Science (PLoS), Oct. 2021, PLOS ONE, 16(10) (10), e0259236 - e0259236, English, International magazine
    [Refereed]
    Scientific journal
    Link to Kobe Univ. Repository (Kernel)

  • Makoto Oishi, Akihiro Mukaino, Misako Kunii, Asami Saito, Yukimasa Arita, Haruki Koike, Osamu Higuchi, Yasuhiro Maeda, Norio Abiru, Naohiro Yamaguchi, Hiroaki Kawano, Eiko Tsuiki, Tomonori Tanaka, Hidenori Matsuo, Masahisa Katsuno, Fumiaki Tanaka, Akira Tsujino, Shunya Nakane
    OBJECTIVE: To determine whether autonomic dysfunction in neurosarcoidosis is associated with anti-ganglionic acetylcholine receptor (gAChR) antibodies, which are detected in autoimmune autonomic ganglionopathy. METHODS: We retrospectively extracted cases of sarcoidosis from 1787 serum samples of 1,381 patients between 2012 and 2018. Anti-gAChR antibodies against the α3 and β4 subunit were measured by luciferase immunoprecipitation to confirm the clinical features of each case. We summarized literature reviews of neurosarcoidosis with severe dysautonomia to identify relevant clinical features and outcomes. RESULTS: We extracted three new cases of neurosarcoidosis with severe dysautonomia, among which two were positive for anti-gAChR antibodies: Case 1 was positive for antibodies against the β4 subunit, and Case 2 was positive for antibodies against both the α3 and β4 subunits. We reviewed the cases of 15 patients with neurosarcoidosis and severe dysautonomia, including the three cases presented herein. Orthostatic hypotension and orthostatic intolerance were the most common symptoms. Among the various types of neuropathy, small fiber neuropathy (SFN) was the most prevalent, with seven of nine cases exhibiting definite SFN. Six of eight cases had impaired postganglionic fibers, of which the present three cases revealed abnormality of 123I-MIBG myocardial scintigraphy. Of the 11 cases, 10 were responsive to immunotherapy, except one seropositive case (Case 2). CONCLUSIONS: The presence of gAChR antibodies may constitute one of the mechanisms by which dysautonomia arises in neurosarcoidosis.
    Apr. 2021, Journal of neurology, 268(11) (11), 4265 - 4279, English, International magazine
    [Refereed]
    Scientific journal

  • Akira Yamagata, Machiko Arita, Hiromasa Tachibana, Fumiaki Tokioka, Chikatoshi Sugimoto, Hiromitsu Sumikawa, Tomonori Tanaka, Hideki Yasui, Tomoyuki Fujisawa, Yutaro Nakamura, Takafumi Suda, Tadashi Ishida
    BACKGROUND: Idiopathic non-specific interstitial pneumonia (iNSIP), idiopathic pleuroparenchymal fibroelastosis (iPPFE), and unclassifiable idiopathic interstitial pneumonia (IIP) are IIPs with chronic fibrotic phenotypes, and unlike idiopathic pulmonary fibrosis, they have often been treated with anti-inflammatory drugs, including corticosteroids and immunosuppressants. However, the impact of bronchoalveolar lavage (BAL) lymphocytosis on the effects of anti-inflammatory therapy has never been evaluated. This study aimed to elucidate whether BAL lymphocytosis can be used to predict the efficacy of anti-inflammatory drugs for iNSIP, iPPFE, and unclassifiable IIP. METHODS: Japanese patients diagnosed with iNSIP, iPPFE, and unclassifiable IIP by multidisciplinary discussion were identified using the nationwide registry. Eligible patients were stratified into four groups with and without BAL lymphocytosis and anti-inflammatory therapy to compare overall survival (OS) and changes in lung function. BAL lymphocytosis was defined as a lymphocyte differential count > 15%, and the cut-off was corroborated by survival classification and regression tree analysis. RESULTS: Overall, 186 patients (37 iNSIP, 16 iPPFE, and 133 unclassifiable IIP) were analyzed. Limited to patients treated with anti-inflammatory drugs (n = 123), patients with BAL lymphocytosis had a better prognosis [hazard ratio (HR), 0.26; 95% confidence interval (CI), 0.11-0.63; P = 0.003], higher slope of forced vital capacity (FVC) % predicted for 2 years, and longer OS (log-rank test, P = 0.012) than those without BAL lymphocytosis. On multivariate analysis, BAL lymphocytosis (HR 0.31; 95% CI 0.13-0.75; P = 0.009) was a prognostic factor for OS, along with age and FVC % predicted. Conversely, for patients managed without anti-inflammatory therapy (n = 63), the presence or absence of BAL lymphocytosis had no prognostic value. CONCLUSIONS: BAL lymphocytosis is associated with good outcomes in patients treated with anti-inflammatory drugs, but has no prognostic value when anti-inflammatory drugs are not used. BAL lymphocytosis may provide a predictive biomarker for identifying patients with iNSIP, iPPFE and unclassifiable IIP who are likely to benefit from anti-inflammatory drugs.
    Apr. 2021, Respiratory research, 22(1) (1), 115 - 115, English, International magazine
    [Refereed]
    Scientific journal

  • Noriyuki Enomoto, Hiromitsu Sumikawa, Hiroaki Sugiura, Masashi Kitani, Tomonori Tanaka, Hironao Hozumi, Tomoyuki Fujisawa, Takafumi Suda
    BACKGROUND: Nonspecific interstitial pneumonia (NSIP) and organizing pneumonia (OP) are major subtypes of idiopathic interstitial pneumonias (IIPs) and closely related to connective tissue diseases (CTDs). "NSIP with OP overlap" is a controversial finding that has recently appeared in the criteria of interstitial pneumonia with autoimmune features (IPAF). However, details of this controversial entity are not well known. OBJECTIVE: To determine the frequency of "NSIP with OP overlap" pattern in IIPs and to identify differences from idiopathic NSIP (iNSIP). METHODS: In 524 patients with interstitial pneumonia from 39 institutes who underwent surgical lung biopsy, 444 were diagnosed as IIPs by a multidisciplinary discussion meeting via a cloud-based integrated database. Among these patients, 44 (9.9%) who had iNSIP and 21 (4.7%) with histopathologically-defined "NSIP with OP overlap" pattern (a pathological NSIP and OP pattern, but without a UIP pattern) were retrospectively studied. RESULTS: Patients with "NSIP with OP overlap" pattern showed a significantly greater extent of consolidation (p < 0.001), more subpleural ground glass attenuation (p = 0.036), and more peripheral + bronchovascular distribution (p = 0.009) on high-resolution computed tomography than those with iNSIP. The incidences of newly-developed CTDs during follow-up was similar between the groups and polymyositis/dermatomyositis was the most frequent CTD in both groups. Nearly half of the patients fulfilled IPAF criteria, but no significant difference was found between iNSIP and "NSIP with OP overlap" pattern (47.7% vs. 42.9, p = 0.712). The incidence of acute exacerbation and the survival rates were similar between the groups. CONCLUSIONS: The incidence of "NSIP with OP overlap" pattern is 4.7% in IIPs. The frequency of newly-developed CTDs during follow-up, mainly polymyositis/dermatomyositis, the frequency of acute exacerbation, and the survival rate in "NSIP with OP overlap" pattern are similar to those of iNSIP.
    Oct. 2020, Respiratory medicine, 174, 106201 - 106201, English, International magazine
    [Refereed]
    Scientific journal

  • Yuta Yoshida, Ippei Matsumoto, Tomonori Tanaka, Kentaro Yamao, Akihiro Hayashi, Keiko Kamei, Shumpei Satoi, Atsushi Takebe, Takuya Nakai, Mamoru Takenaka, Yoshifumi Takeyama
    BACKGROUND: Pancreatic pleural effusion and ascites are defined as fluid accumulation in the thoracic and abdominal cavity, respectively, due to direct leakage of the pancreatic juice. They usually occur in patients with acute or chronic pancreatitis but are rarely associated with pancreatic neoplasm. We present here an extremely rare case of pancreatic neuroendocrine tumor with stenosis of the main pancreatic duct, leading to pancreatic pleural effusion. CASE PRESENTATION: A 51-year-old man complained of dyspnea. Left-sided pleural effusion was detected on the chest X-ray. Pleural puncture was performed, and the pleural fluid indicated a high amylase content (36,854 IU/L). Hence, the patient was diagnosed with pancreatic pleural effusion. Although no tumor was detected, the computed tomography (CT) scan showed a pseudocyst and dilation of the main pancreatic duct in the pancreatic tail. Magnetic resonance cholangiopancreatography showed a fistula from the pseudocyst into the left thoracic cavity. Endoscopic retrograde pancreatic drainage was attempted; however, it failed due to stenosis in the main pancreatic duct in the pancreatic body. Endoscopic ultrasound revealed a hypoechoic mass measuring 15 × 15 mm in the pancreatic body that was not enhanced in the late phase of contrast perfusion and was thus suspected to be an invasive ductal carcinoma. The patient underwent distal pancreatectomy with splenectomy and the postoperative course was uneventful. Histopathological examination confirmed a neuroendocrine tumor of the pancreas (NET G2). The main pancreatic duct was compressed by the tumor. Increased pressure on the distal pancreatic duct by the tumor might have caused formation of the pseudocyst and pleural effusion. To the best of our knowledge, this is the first case report of pancreatic pleural effusion associated with a neuroendocrine tumor. CONCLUSIONS: Differential diagnosis of a pancreatic neoplasm should be considered, especially when a patient without a history of pancreatitis presents with pleural effusion.
    Sep. 2020, Surgical case reports, 6(1) (1), 222 - 222, English, International magazine
    [Refereed]
    Scientific journal

  • Yuzo Suzuki, Tomoyuki Fujisawa, Hiromitsu Sumikawa, Tomonori Tanaka, Chikatoshi Sugimoto, Masato Kono, Hironao Hozumi, Masato Karayama, Kazuki Furuhashi, Noriyuki Enomoto, Yutaro Nakamura, Naoki Inui, Takafumi Suda
    BACKGROUND: Idiopathic pleuroparenchymal fibroelastosis (iPPFE) is a rare interstitial lung disease characterized by unique radiological and pathological findings. However, pathological evaluations are available only in a limited number of patients. Therefore, several clinical diagnostic criteria have been proposed. Nevertheless, the applicability of these criteria has not yet been validated. Moreover, the clinical course of iPPFE and its prognosis have not yet been completely elucidated. METHODS: The present study assessed previously proposed clinical diagnostic criteria by comparing the clinical features between pathologically diagnosed iPPFE (p-iPPFE) and clinically diagnosed iPPFE (c-iPPFE). Subsequently, the clinical features of iPPFE were characterized and compared with those of idiopathic pulmonary fibrosis (IPF, n = 323). RESULTS: Clinical characteristics of c-iPPFE (n = 27) and p-iPPFE (n = 35) were similar. No significant difference was observed in terms of prognosis between c-iPPFE and p-iPPFE. The number of patients with iPPFE (both c-iPPFE and p-iPPFE) who developed lung cancer was significantly lower than that of patients with IPF. However, acute exacerbation (AE) showed similar incidence in patients with iPPFE and IPF. Survival of patients with iPPFE was significantly worse than that of patients with IPF (5-year survival rate: 38.5% vs. 63.5%, p < 0.0001), and the most common cause of death was chronic respiratory failure (73.8%), followed by AE (14.3%). Male gender was the only poor prognostic factor of iPPFE. CONCLUSION: The present study demonstrated efficiency of clinical diagnosis and also revealed clinically important characteristics of iPPFE that should be considered for management of iPPFE.
    Sep. 2020, Respiratory medicine, 171, 106078 - 106078, English, International magazine
    [Refereed]
    Scientific journal

  • Jun Fukihara, Yasuhiro Kondoh, Kevin K. Brown, Tomoki Kimura, Kensuke Kataoka, Toshiaki Matsuda, Yasuhiko Yamano, Atsushi Suzuki, Taiki Furukawa, Hiromitsu Sumikawa, Osamu Takahashi, Takeshi Johkoh, Tomonori Tanaka, Junya Fukuoka, Naozumi Hashimoto, Yoshinori Hasegawa
    Recent studies have suggested that in patients with an idiopathic interstitial pneumonia (IIP), a probable usual interstitial pneumonia (UIP) pattern on chest computed tomography (CT) is sufficient to diagnose idiopathic pulmonary fibrosis (IPF) without histopathology. We retrospectively compared the prognosis and time to first acute exacerbation (AE) in IIP patients with a UIP and a probable UIP pattern on initial chest CT. One hundred and sixty IIP patients with a UIP pattern and 242 with a probable UIP pattern were identified. Probable UIP pattern was independently associated with longer survival time (adjusted hazard ratio 0.713, 95% CI 0.536–0.950; p=0.021) and time to first AE (adjusted hazard ratio 0.580, 95% CI 0.389–0.866; p=0.008). In subjects with a probable UIP pattern who underwent surgical lung biopsy, the probability of a histopathological UIP pattern was 83%. After multidisciplinary discussion and the inclusion of longitudinal behaviour, a diagnosis of IPF was made in 66% of cases. In IPF patients, survival time and time to first AE were not associated with CT pattern. Among subjects with a probable UIP pattern, compared to non-IPF patients, survival time and time to first AE were shorter in IPF patients. In conclusion, IIP patients with a probable UIP pattern on initial chest CT had a better prognosis and longer time to first AE than those with a UIP pattern. However, when baseline data and longitudinal behaviour provided a final diagnosis of IPF, CT pattern was not associated with these outcomes. This suggests diagnostic heterogeneity among patients with a probable UIP pattern.
    European Respiratory Society (ERS), Apr. 2020, European Respiratory Journal, 55(4) (4), 1802465 - 1802465
    [Refereed]
    Scientific journal

  • Nobuyasu Awano, Minoru Inomata, Naoyuki Kuse, Mari Tone, Hanako Yoshimura, Tatsunori Jo, Kohei Takada, Chikatoshi Sugimoto, Tomonori Tanaka, Hiromitsu Sumikawa, Yuzo Suzuki, Tomoyuki Fujisawa, Takafumi Suda, Takehiro Izumo
    BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a progressive disease often accompanied by skeletal muscle wasting. We investigated whether skeletal muscle mass and muscle attenuation on computed tomography (CT) are predictors of mortality in IPF patients, using a nationwide cloud-based database and web-based multidisciplinary discussion (MDD) system. METHODS: IPF patients diagnosed using MDD from April 2009 to March 2014 were included. We analyzed the cross-sectional area (CSA) of the erector spinae muscle (ESMCSA) and the pectoralis muscle (PMCSA), muscle attenuation of the ESM (ESMMA), and PM (PMMA) on single-slice axial CT. Survival probability was assessed using the Kaplan-Meier method and compared by the log-rank test. Multivariate Cox proportional hazards models were used to evaluate the relationship among the ESMCSA, PMCSA, ESMMA, PMMA, clinical parameters, and prognosis. RESULTS: A total of 199 IPF patients were enrolled. Seventy-four patients died during the study period and the most frequent cause was acute exacerbation (13.1%). The group with the lowest quartile of ESMCSA had significantly worse survival than other groups (P = 0.009). Survival rates of the groups with the lowest quartile of PMCSA, lower ESMMA, and lower PMMA did not differ from those of other groups. According to multivariate analysis, ESMCSA < lower quartile was significantly associated with all-cause mortality (hazards ratio, 1.96; P = 0.030), whereas, ESMMA < median, PMCSA < lower quartile, and PMMA < median were not. CONCLUSIONS: Low ESMCSA on CT images may be a strong risk factor for all-cause mortality in IPF patients based on MDD diagnosis.
    Mar. 2020, Respiratory investigation, 58(2) (2), 91 - 101, English, International magazine
    [Refereed]
    Scientific journal

  • Makiko Murota, Takeshi Johkoh, Kyung Soo Lee, Tomas Franquet, Yasuhiro Kondoh, Yoshihiro Nishiyama, Tomonori Tanaka, Hiromitsu Sumikawa, Ryoko Egashira, Norihiko Yamaguchi, Kiminori Fujimoto, Junya Fukuoka
    Purpose: To describe computed tomography (CT) findings of influenza H1N1 virus-associated pneumonia (IH1N1VAP), and to correlate CT findings to pathological ones. Methods: The study included 24 patients with IH1N1VAP. Two observers independently evaluated the presence, distribution, and extent of CT findings. CT features were divided into either classical form (C-form) or non-classical form (NC-form). C-form included: A.) broncho-bronchiolitis and bronchopneumonia type, whereas NC-forms included: B.) diffuse peribronchovascular type, simulating subacute rheumatoid arthritis-associated (RA) interstitial lung disease (ILD) and C.) lower peripheral and/or peribronchovascular type, resembling dermatomyositis-associated ILD and COVID-19 pneumonia. In 10 cases with IH1N1VAP where lung biopsy was performed, CT and pathology findings were correlated. Results: The most common CT findings were ground-glass opacities (24/24, 100 %) and airspace consolidation (23/24, 96 %). C-form was found in 11 (46 %) patients while NC-form in 13 (54 %). Types A, B, and C were seen in 11(46 %), 4 (17 %), and 9 (38 %) patients, respectively. The lung biopsy revealed organizing pneumonia in all patients and 6 patients (60 %) showed incorporated type organizing pneumonia that was common histological findings of rapidly progressive ILD. Conclusion: In almost half of patients of IH1N1VAP, CT images show NC-form pneumonia pattern resembling either acute or subacute RA or dermatomyositis-associated ILD and COVID-19 pneumonia.
    2020, European journal of radiology open, 7, 100297 - 100297, English, International magazine
    [Refereed]
    Scientific journal

  • Acute exacerbations of fibrotic interstitial lung diseases.
    Suzuki A, Kondoh Y, Brown KK, Johkoh T, Kataoka K, Fukuoka J, Kimura T, Matsuda T, Yokoyama T, Fukihara J, Ando M, Tanaka T, Hashimoto N, Sakamoto K, Hasegawa Y
    Aug. 2019, Respirology, English
    [Refereed]
    Scientific journal

  • Cancer-associated Retinopathy with Neuroendocrine Combined Large-cell Lung Carcinoma and Adenocarcinoma: A Case Report.
    Yagyu K, Ueda T, Miyamoto A, Uenishi R, Matsushita H, Tanaka T
    Jul. 2019, Internal medicine, English
    [Refereed]
    Scientific journal

  • Noriyuki Enomoto, Ryoko Egashira, Kazuhiro Tabata, Mikiko Hashisako, Masashi Kitani, Yuko Waseda, Tamotsu Ishizuka, Satoshi Watanabe, Kazuo Kasahara, Shinyu Izumi, Akira Shiraki, Atsushi Miyamoto, Kazuma Kishi, Tomoo Kishaba, Chikatosi Sugimoto, Yoshikazu Inoue, Kensuke Kataoka, Yasuhiro Kondoh, Yutaka Tsuchiya, Tomohisa Baba, Hiroaki Sugiura, Tomonori Tanaka, Hiromitsu Sumikawa, Takafumi Suda
    Thoracic diseases in patients with systemic lupus erythematosus (SLE), especially interstitial pneumonia (SLE-IP), are rare and have been poorly studied. The aims of this multicentre study were to evaluate SLE-IP and elucidate its clinical characteristics and prognosis. Fifty-five patients with SLE-IP who had attended the respiratory departments of participating hospitals were retrospectively evaluated in this multicentre study. Clinical information, high-resolution computed tomography (HRCT), and surgical lung biopsy/autopsy specimens were analysed by respiratory physicians, pulmonary radiologists, and pulmonary pathologists. IP patterns on HRCT and lung specimens were classified based on the international classification statement/guideline for idiopathic interstitial pneumonias. The most frequent form of SLE-IP at diagnosis was chronic IP (63.6%), followed by subacute (20.0%), and acute IP (12.7%). Radiologically, the most common HRCT pattern was "Unclassifiable" (54%). Histologically, "Unclassifiable" was the most frequently found (41.7%) among 12 patients with histologically proven IP. Interestingly, accompanying airway diseases were present in nine of these patients (75%). In multivariate analysis, current smoking (hazard ratio [HR] 6.105, p = 0.027), thrombocytopenia (HR 7.676, p = 0.010), anti-double-strand DNA titre (HR 0.956, p = 0.027), and nonspecific interstitial pneumonia (NSIP) + organizing pneumonia (OP) pattern on HRCT (vs. NSIP, HR 0.089, p = 0.023) were significant prognostic factors. In conclusion, chronic IP was the most frequent form of IP in patients with SLE-IP, and "Unclassifiable" was the commonest pattern radiologically and histologically.
    May 2019, Scientific reports, 9(1) (1), 7355 - 7355, English, International magazine
    [Refereed]
    Scientific journal

  • Tomoyuki Fujisawa, Kazutaka Mori, Masashi Mikamo, Takashi Ohno, Kensuke Kataoka, Chikatoshi Sugimoto, Hideya Kitamura, Noriyuki Enomoto, Ryoko Egashira, Hiromitsu Sumikawa, Tae Iwasawa, Shoichiro Matsushita, Hiroaki Sugiura, Mikiko Hashisako, Tomonori Tanaka, Yasuhiro Terasaki, Shinobu Kunugi, Masashi Kitani, Ryo Okuda, Yasuoki Horiike, Yasunori Enomoto, Hideki Yasui, Hironao Hozumi, Yuzo Suzuki, Yutaro Nakamura, Junya Fukuoka, Takeshi Johkoh, Yasuhiro Kondoh, Takashi Ogura, Yoshikazu Inoue, Yoshinori Hasegawa, Naohiko Inase, Sakae Homma, Takafumi Suda
    Multidisciplinary discussion (MDD) requiring close communication between specialists (clinicians, radiologists and pathologists) is the gold standard for the diagnosis of idiopathic interstitial pneumonias (IIPs). However, MDD by specialists is not always feasible because they are often separated by time and location. An online database would facilitate data sharing and MDD. Our aims were to develop a nationwide cloud-based integrated database containing clinical, radiological and pathological data of patients with IIPs along with a web-based MDD system, and to validate the diagnostic utility of web-based MDD in IIPs.Clinical data, high-resolution computed tomography images and lung biopsy slides from patients with IIPs were digitised and uploaded to separate servers to develop a cloud-based integrated database. Web-based MDD was performed using the database and video-conferencing to reach a diagnosis.Clinical, radiological and pathological data of 524 patients in 39 institutions were collected, uploaded and incorporated into the cloud-based integrated database. Subsequently, web-based MDDs with a pulmonologist, radiologist and pathologist using the database and video-conferencing were successfully performed for the 465 cases with adequate data. Overall, the web-based MDD changed the institutional diagnosis in 219 cases (47%). Notably, the MDD diagnosis yielded better prognostic separation among the IIPs than did the institutional diagnosis.This is the first study of developing a nationwide cloud-based integrated database containing clinical, radiological and pathological data for web-based MDD in patients with IIPs. The database and the web-based MDD system that we built made MDD more feasible in practice, potentially increasing accurate diagnosis of IIPs.
    May 2019, The European respiratory journal, 53(5) (5), English, International magazine
    [Refereed]
    Scientific journal

  • 胃異物沈着症の2例
    筑後 孝章, 大谷 知之, 田中 伴典, 榎木 英介, 前西 修, 清水 重喜, 木村 雅友, 南野 弘明, 佐藤 隆夫
    (一社)日本病理学会, Apr. 2019, 日本病理学会会誌, 108(1) (1), 367 - 367, Japanese

  • 本学の病理学教育へのWhole Slide Imaging導入の現状
    筑後 孝章, 大谷 知之, 田中 伴典, 榎木 英介, 前西 修, 清水 重喜, 木村 雅友, 佐藤 隆夫, 伊藤 彰彦
    (一社)日本病理学会, Apr. 2019, 日本病理学会会誌, 108(1) (1), 440 - 440, Japanese

  • 胸腔鏡下肺生検で診断した軽症の多中心性キャッスルマン病の1例
    佐伯 翔, 西山 理, 田中 伴典, 佐野 安希子, 岩永 賢司, 東田 有智
    (一社)日本呼吸器学会, Sep. 2018, 日本呼吸器学会誌, 7(5) (5), 342 - 346, Japanese
    [Refereed]

  • Update on Rare Idiopathic Interstitial Pneumonias and Rare Histologic Patterns.
    Tomonori Tanaka, Kaori Ishida
    Sep. 2018, Archives of Pathology and Laboratory Medicine, 142(9) (9), 1069 - 1079, English
    [Refereed][Invited]
    Scientific journal

  • Kazuki Okamoto, Tomohiro Watanabe, Yoriaki Komeda, Ayana Okamoto, Kosuke Minaga, Ken Kamata, Kentaro Yamao, Mamoru Takenaka, Satoru Hagiwara, Toshiharu Sakurai, Tomonori Tanaka, Hiroki Sakamoto, Kiyoshige Fujimoto, Naoshi Nishida, Masatoshi Kudo
    Frontiers Media SA, May 2018, Frontiers in Immunology, 9, English
    [Refereed]
    Scientific journal

  • Mutsumi Ozasa, Hiromi Ichikawa, Shuntaro Sato, Tomonori Tanaka, Takeshi Johkoh, Kensuke Kataoka, Yasuhiko Yamano, Yasuhiro Kondoh, Hideki Nakamura, Atsushi Kawakami, Andrey Bychkov, Hiroyuki Taniguchi, Junya Fukuoka
    OBJECTIVES: Idiopathic interstitial pneumonia (IIP) and connective tissue disease -associated interstitial pneumonia (CTD-IP) are the two most common types of interstitial pneumonia. IIP and CTD-IP share common histological features, yet their clinical management is different. Separation of the two conditions based solely on histology can be challenging, and there are no established criteria. MATERIALS AND METHODS: We selected 105 consecutive cases of IIP (79 usual interstitial pneumonia and 26 non-specific interstitial pneumonia) and 49 cases of CTD-IP for derivation and 32 cases of IIP and 10 cases of CTD-IP for validation. Fourteen histological parameters were evaluated independently by two pathologists for derivation group and graded into 0 to 3. The association between the score for each marker and a diagnosis of CTD was investigated using Fisher's exact test and stepwise logistic regression analysis. A formula for calculating the probability of IIP and CTD-IP was constructed by the markers identified in the regression test with coefficients for each finding. The formula was confirmed using validation case group. RESULTS: Stepwise logistic regression analysis showed that plasmacytosis, lymphoid follicle with germinal center, and airspace fibrin were suggestive of CTD-IP and that fibroblastic foci, smooth muscle hyperplasia, cellular IP, dense perivascular collagen, and fat metaplasia were suggestive of IIP. The formula used to calculate the probabilities based on estimated values for each finding was created, and user-friendly web based app was composed at www.ctdip.com. On the validation study, 30 out of 32 IIP and eight out of 10 CTD-IPs were distinguished correctly by the app (Specificity: 93%, Sensitivity: 80%). CONCLUSIONS: We identified histological markers and derived a practical formula and user-friendly app to distinguish CTD-IPs from IIP.
    2018, PloS one, 13(11) (11), e0206186, English, International magazine
    [Refereed]
    Scientific journal

  • Azusa Yoneshige, Man Hagiyama, Takao Inoue, Tomonori Tanaka, Aritoshi Ri, Akihiko Ito
    Oct. 2017, MOLECULAR NEUROBIOLOGY, 54(8) (8), 6378 - 6390, English
    [Refereed]
    Scientific journal

  • Emiko Udo, Bungo Furusato, Kazuko Sakai, Leah M. Prentice, Tomonori Tanaka, Yuka Kitamura, Tomoshi Tsuchiya, Naoya Yamasaki, Takeshi Nagayasu, Kazuto Nishio, Junya Fukuoka
    Aug. 2017, DIAGNOSTIC PATHOLOGY, 12(1) (1), 62 - 66, English
    [Refereed]
    Scientific journal

  • Mikiko Hashisako, Tomonori Tanaka, Yasuhiro Terasaki, Toshimasa Uekusa, Rosane D. Achcar, Bassam I. Aswad, Hanaa S. Bamefleh, Vera L. Capelozzi, John C. English, Alexandre T. Fabro, Kensuke Kataoka, Tomayoshi Hayashi, Yasuhiro Kondoh, Hiroyuki Taniguchi, Junya Fukuoka
    Dec. 2016, ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 140(12) (12), 1375 - 1382, English
    [Refereed]
    Scientific journal

  • Yoshihiro Ohue, Koji Kurose, Ryohei Nozawa, Midori Isobe, Yumi Nishio, Tomonori Tanaka, Yoshinori Doki, Takashi Hori, Junya Fukuoka, Mikio Oka, Eiichi Nakayama
    Dec. 2016, CANCER IMMUNOLOGY RESEARCH, 4(12) (12), 1049 - 1060, English
    [Refereed]
    Scientific journal

  • Kunihiro Ichinose, Saeko Araki, Ayuko Takatani, Tomonori Tanaka, Atsushi Kawakami
    Sep. 2016, ARTHRITIS & RHEUMATOLOGY, 68(9) (9), 2256 - 2256, English
    [Refereed]
    Scientific journal

  • Hideji Otani, Tomonori Tanaka, Kiyoshi Murata, Junya Fukuoka, Norihisa Nitta, Yukihiro Nagatani, Akinaga Sonoda, Masashi Takahashi
    Dove Medical Press Ltd., Jul. 2016, International Journal of COPD, 11(1) (1), 1521 - 1532, English
    [Refereed]
    Scientific journal

  • Sayuri Nunomura, Tomonori Tanaka, Toshiyuki Nakayama, Kyoko Otani, Haruyuki Ishii, Kazuhiro Tabata, Yasuhiro Kondoh, Kensuke Kataoka, Takeshi Johkoh, Hiroyuki Taniguchi, Junya Fukuoka
    Elsevier B.V., Jul. 2016, Respiratory Investigation, 54(4) (4), 272 - 279, English
    [Refereed]
    Scientific journal

  • Akira Yoshikawa, Shuntaro Sato, Tomonori Tanaka, Mikiko Hashisako, Yukio Kashima, Tomoshi Tsuchiya, Naoya Yamasaki, Takeshi Nagayasu, Hiroshi Yamamoto, Junya Fukuoka
    2016, INTERNATIONAL JOURNAL OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE, 11, 19 - 26, English
    [Refereed]
    Scientific journal

  • Hideji Otani, Tomonori Tanaka, Kiyoshi Murata, Junya Fukuoka, Norihisa Nitta, Yukihiro Nagatani, Akinaga Sonoda, Masashi Takahashi
    2016, INTERNATIONAL JOURNAL OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE, 11, 1521 - 1532, English
    [Refereed]
    Scientific journal

  • Akira Yoshikawa, Shuntaro Sato, Tomonori Tanaka, Mikiko Hashisako, Yukio Kashima, Tomoshi Tsuchiya, Naoya Yamasaki, Takeshi Nagayasu, Hiroshi Yamamoto, Junya Fukuoka
    PURPOSE: Pulmonary emphysema is the pathological prototype of chronic obstructive pulmonary disease and is also associated with other lung diseases. We considered that observation with different approaches may provide new insights for the pathogenesis of emphysema. PATIENTS AND METHODS: We reviewed tissue blocks of the lungs of 25 cases with/without emphysema and applied a three-dimensional observation method to the blocks. Based on the three-dimensional characteristics of the alveolar structure, we considered one face of the alveolar polyhedron as a structural unit of alveoli and called it a framework unit (FU). We categorized FUs based on their morphological characteristics and counted their number to evaluate the destructive changes in alveoli. We also evaluated the number and the area of pores of Kohn in FUs. We performed linear regression analysis to estimate the effect of these data on pulmonary function tests. RESULTS: In multivariable regression analysis, a decrease in the number of FUs without an alveolar wall led to a significant decrease in the diffusing capacity of the lung for carbon monoxide (DLCO) and DLCO per unit alveolar volume, and an increase in the area of pores of Kohn had a significant effect on an increase in residual capacity. CONCLUSION: A breakdown in the lung framework and an increase in pores of Kohn are associated with a decrease in DLCO and DLCO per unit alveolar volume with/without emphysema.
    2016, International journal of chronic obstructive pulmonary disease, 11, 2287 - 2294, English, International magazine
    [Refereed]
    Scientific journal

  • Ryusuke Machino, Naoya Yamasaki, Takurou Miyazaki, Keitarou Matsumoto, Tomoshi Tsuchiya, Tomonori Tanaka, Hideyuki Hayashi, Kazuto Ashizawa, Takeshi Nagayasu
    Nov. 2015, JOURNAL OF THORACIC IMAGING, 30(6) (6), W76 - W79, English
    [Refereed]
    Scientific journal

  • Hiroki Karata, Tomonori Tanaka, Ryoko Egashira, Kazuhiro Tabata, Kyoko Otani, Ryuji Hayashi, Takashi Hori, Junya Fukuoka
    Dove Medical Press Ltd., Jul. 2015, International Journal of COPD, 10, 1299 - 1303, English
    [Refereed]
    Scientific journal

  • Takeshi Johkoh, Junya Fukuoka, Tomonori Tanaka
    Mar. 2015, EUROPEAN JOURNAL OF RADIOLOGY, 84(3) (3), 542 - 546, English
    [Refereed]
    Scientific journal

  • Yasuhiro Kondoh, Takeshi Johkoh, Junya Fukuoka, Hiroaki Arakawa, Tomonori Tanaka, Naohiro Watanabe, Koji Sakamoto, Kensuke Kataoka, Tomoki Kimura, Hiroyuki Taniguchi
    Mar. 2015, RESPIRATORY MEDICINE, 109(3) (3), 389 - 396, English
    [Refereed]
    Scientific journal

  • Hiroki Karata, Tomonori Tanaka, Ryoko Egashira, Kazuhiro Tabata, Kyoko Otani, Ryuji Hayashi, Takashi Hori, Junya Fukuoka
    2015, INTERNATIONAL JOURNAL OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE, 10, 1299 - 1303, English
    [Refereed]
    Scientific journal

  • Kazuhiro Tabata, Tomonori Tanaka, Tomayoshi Hayashi, Takashi Hori, Sayuri Nunomura, Suguru Yonezawa, Junya Fukuoka
    BioMed Central Ltd., May 2014, BMC Clinical Pathology, 14(1) (1), 23, English
    [Refereed]
    Scientific journal

  • Yuki Hara, Tomonori Tanaka, Kazuhiro Tabata, Akira Shiraki, Kentaro Hayashi, Yukio Kashima, Tomayoshi Hayashi, Junya Fukuoka
    Mar. 2014, PATHOLOGY INTERNATIONAL, 64(3) (3), 148 - 150, English
    [Refereed]

  • Takeshi Johkoh, Hiromotsu Sumikawa, Junya Fukuoka, Tomonori Tanaka, Kiminori Fujimoto, Masashi Takahashi, Noriyuki Tomiyama, Yasuhiro Kondo, Hiroyuki Taniguchi
    Jan. 2014, EUROPEAN JOURNAL OF RADIOLOGY, 83(1) (1), 20 - 26, English
    [Refereed]
    Scientific journal

  • Junya Fukuoka, Masaki Tominaga, Kazuya Ichikado, Tomonori Tanaka, Hidenori Ichiyasu, Hirotsugu Kohrogi, Shin Ishizawa, Moritaka Suga
    Feb. 2013, Pathology International, 63(2) (2), 108 - 112, English
    [Refereed]
    Scientific journal

  • Ryoko Egashira, Tomonori Tanaka, Takeshi Imaizumi, Kazutaka Senda, Yoshinori Doki, Sho Kudo, Junya Fukuoka
    Feb. 2013, RESPIROLOGY, 18(2) (2), 348 - 353, English
    [Refereed]
    Scientific journal

  • Tomayoshi Hayashi, Hisao Sano, Ryoko Egashira, Kazuhiro Tabata, Tomonori Tanaka, Toshiyuki Nakayama, Yukio Kashima, Takashi Hori, Sayuri Nunomura, Junya Fukuoka
    2013, BioMed Research International, 2013, 157838, English
    [Refereed]
    Scientific journal

  • Tomonori Tanaka, Kyoko Otani, Ryoko Egashira, Yukio Kashima, Hiroyuki Taniguchi, Yasuhiro Kondoh, Kensuke Kataoka, Akira Shiraki, Yasuhiko Kitasato, Kevin O. Leslie, Junya Fukuoka
    Dec. 2012, RESPIRATORY MEDICINE, 106(12) (12), 1765 - 1770, English
    [Refereed]
    Scientific journal

  • Junya Fukuoka, Matthias D. Hofer, Takashi Hori, Tomonori Tanaka, Shin Ishizawa, Kazuhiro Nomoto, Manami Saito, Takeshi Uemura, Lucian R. Chirieac
    Nov. 2012, ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 136(11) (11), 1377 - 1384, English
    [Refereed]
    Scientific journal

  • Jun Nishikawa, Tomonori Tanaka, Toshiro Sugiyama
    Nov. 2012, CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 10(11) (11), A24 - A24, English
    [Refereed]

  • Sanjay Mukhopadhyay, Carol F. Farver, Laszlo T. Vaszar, Owen J. Dempsey, Helmut H. Popper, Haresh Mani, Vera L. Capelozzi, Junya Fukuoka, Keith M. Kerr, E. Handan Zeren, Venkateswaran K. Iyer, Tomonori Tanaka, Ivy Narde, Angheliki Nomikos, Derya Gumurdulu, Sudheer Arava, Dani S. Zander, Henry D. Tazelaar
    Jan. 2012, JOURNAL OF CLINICAL PATHOLOGY, 65(1) (1), 51 - 57, English
    [Refereed]
    Scientific journal

  • Masanori Nakanishi, Junya Fukuoka, Tomonori Tanaka, Yoshiki Demura, Yukihiro Umeda, Shingo Ameshima, Satoshi Nishikawa, Masanori Kitaichi, Harumi Itoh, Takeshi Ishizaki
    Dec. 2011, RESPIRATORY MEDICINE, 105(12) (12), 1931 - 1938, English
    [Refereed]
    Scientific journal

  • Kishio Kuroda, Shin Ishizawa, Takahiko Kudo, Hideyuki Uotani, Ayumu Hosokawa, Tomonori Tanaka, Haruhisa Kitano, Takashi Hori, Kazuhiro Tsukada, Toshiro Sugiyama, Junya Fukuoka
    Apr. 2008, PATHOLOGY INTERNATIONAL, 58(4) (4), 239 - 243, English
    [Refereed]
    Scientific journal

  • Shinobu Kawamura, Takafumi Nakamura, Takeshi Oya, Shin Ishizawa, Yuta Sakai, Tomonori Tanaka, Shigeru Saito, Junya Fukuoka
    Apr. 2007, PATHOLOGY INTERNATIONAL, 57(4) (4), 213 - 218, English
    [Refereed]
    Scientific journal

■ MISC
  • Exploration for standardization of pathological evaluation in IPF guideline
    小山涼子, 田中伴典, 功刀しのぶ, 財前圭晃, 田畑和宏, 近藤康博, 蛇澤晶, 福岡順也
    2025, 日本病理学会会誌, 114(1) (1)

  • Standardisation study of pathological diagnosis in transbronchial lung cryobiopsy
    財前圭晃, 財前圭晃, 寺崎泰弘, 蛇澤晶, 石田佳央理, 橋迫美貴子, 松村舞依, 木谷匡志, 功刀しのぶ, 田中伴典, 田畑和宏, 澤住知枝, 奥寺康司, 武村民子, 福岡順也
    2025, 日本呼吸器学会誌(Web), 14

  • Combined Hypersensitivity Pneumonitis and Connective Tissue Disease
    井上義一, 井上義一, 澄川裕充, 澄川裕充, 清水重喜, 清水重喜, 香川智子, 香川智子, 馬場智尚, 冨岡洋海, 竹内奈緒子, 竹内奈緒子, 武井玲生仁, 山野泰彦, 久瀬雄介, 久瀬雄介, 村岡達哉, 古澤春彦, 新谷亮多, 新谷亮多, 江頭玲子, 上甲剛, 武村民子, 河端美則, 北市正則, 小倉高志, 近藤康博, 宮崎泰成, 槇野茂樹, 冨永循哉, 田中伴典, 新井徹, 新井徹
    2024, 日本呼吸器学会誌(Web), 13

  • Fibrotic hypersensitivity pneumonia radiologically mostly suggestive I-PPFE
    新井徹, 織田恒幸, 近藤康博, 冨岡洋海, 富井啓介, 宮崎泰成, 竹内奈緒子, 香川智子, 滝本宜之, 井上義一, 冨永循哉, 江頭玲子, 上甲剛, 田中伴典, 笠井孝彦, 寺崎泰弘, 武村民子, 河端美則, 澄川裕充, 清水重喜
    2024, 日本呼吸器学会誌(Web), 13

  • 田中 伴典
    (株)文光堂, Apr. 2023, 病理と臨床, 41(臨増) (臨増), 13 - 13, Japanese

  • 田中 伴典
    (株)文光堂, Apr. 2023, 病理と臨床, 41(臨増) (臨増), 14 - 14, Japanese

  • 藤本 昌大, 立原 素子, 桂田 直子, 田中 伴典, 大木元 愛子, 高宮 麗, 山田 潤, 佐藤 宏紀, 小林 和幸
    (NPO)日本呼吸器内視鏡学会, Mar. 2023, 気管支学, 45(2) (2), 164 - 164, Japanese

  • 呼吸器 IP合併肺がん手術後の急性増悪 間質性肺炎合併肺がん術後急性増悪を病理から考える
    田中 伴典
    日本画像医学会, Feb. 2023, Japanese Journal of Diagnostic Imaging, 41(増刊) (増刊), 79 - 79, Japanese

  • 進行肺扁平上皮癌の治療経過中に良性の多発リンパ節腫大と再考し切除した1例
    伊賀 脩介, 桂田 直子, 立原 素子, 山本 正嗣, 小林 和幸, 光井 卓, 田中 雄悟, 眞庭 謙昌, 田中 伴典
    (NPO)日本肺癌学会, Oct. 2022, 肺癌, 62(5) (5), 444 - 444, Japanese

  • ベキサロテン内服と全身皮膚電子線照射療法の併用が奏効したCD4陰性CD8陰性皮膚T細胞リンパ腫の1例
    高橋 和嘉子, 福本 毅, 谷川 絢乃, 中村 維文, 中野 英司, 国定 充, 錦織 千佳子, 田中 伴典, 伊藤 智雄
    (公社)日本皮膚科学会, Mar. 2022, 日本皮膚科学会雑誌, 132(3) (3), 507 - 507, Japanese

  • 病理解剖における間質性肺炎診断 剖検での間質性肺炎症例におけるCPCの論点
    田中 伴典
    (一社)日本病理学会, Mar. 2022, 日本病理学会会誌, 111(1) (1), 161 - 161, Japanese

  • 過敏性肺炎における気道中心性線維化(ACF)の一致度
    関 来未, 田中 伴典, 奥寺 康司, 財前 圭晃, 加島 志郎, 功刀 しのぶ, 齊藤 涼子, 蛇澤 晶, 福岡 順也
    (一社)日本病理学会, Mar. 2022, 日本病理学会会誌, 111(1) (1), 322 - 322, Japanese

  • 蜂巣 智也, 塚本 龍子, 吉田 美帆, 神保 直江, 芝地 朱音, 中西 大地, 大浦 季恵, 須广 佑介, 猪原 千愛, 古澤 哲嗣, 京竹 愛子, 今川 奈央子, 田中 伴典, 伊藤 智雄
    (公社)日本臨床細胞学会, Oct. 2021, 日本臨床細胞学会雑誌, 60(Suppl.2) (Suppl.2), 580 - 580, Japanese

  • 神保 直江, 吉田 美帆, 塚本 龍子, 南 和宏, 田中 雄悟, 眞庭 謙昌, 河原 邦光, 田中 伴典, 伊藤 智雄
    (公社)日本臨床細胞学会, May 2021, 日本臨床細胞学会雑誌, 60(Suppl.1) (Suppl.1), 138 - 138, Japanese

  • 西山 理, 佐伯 翔, 御勢 久也, 吉川 和也, 東田 有智, 山崎 亮, 田中 伴典, 杉本 親寿, 澄川 裕充, 穗積 宏尚, 藤澤 朋幸, 須田 隆文
    (一社)日本呼吸器学会, Apr. 2021, 日本呼吸器学会誌, 10(増刊) (増刊), 225 - 225, Japanese

  • 間質性肺炎のガイドライン診断 特発性肺線維症のガイドライン診断
    田中 伴典
    (一社)日本病理学会, Mar. 2021, 日本病理学会会誌, 110(1) (1), 169 - 169, Japanese

  • コロナ禍における2つの独立ラインを用いたデジタルリモートカンファレンスの有用性
    関 来未, 佐野 寿郎, 田中 伴典, 田中 秀典, 富沢 健二, 覚道 健一, 福岡 順也
    (一社)日本病理学会, Mar. 2021, 日本病理学会会誌, 110(1) (1), 264 - 264, Japanese

  • 局所的に肺線維性瘢痕に似た通常型間質性肺炎パターン(Localized Lung Fibrotic Scar mimicking Usual Interstitial Pneumonia like Pattern)
    田中 伴典, 兵頭 俊記, 神保 直江, 石田 佳央理, 伊藤 智雄
    (一社)日本病理学会, Mar. 2021, 日本病理学会会誌, 110(1) (1), 293 - 293, English

  • 局所的にMTAP lossとp16ホモ欠失が見られた胸膜mesothelioma in situの1症例
    神保 直江, 平社 亜沙子, 田中 伴典, 吉田 美帆, 塚本 龍子, 伊藤 智雄
    (一社)日本病理学会, Mar. 2021, 日本病理学会会誌, 110(1) (1), 296 - 296, Japanese

  • 絨毛癌成分を伴う浸潤性膵管癌の一例
    菅野 天裕, 小松 正人, 田中 伴典, 伊藤 智雄
    (一社)日本病理学会, Mar. 2021, 日本病理学会会誌, 110(1) (1), 316 - 316, Japanese

  • 塚本 龍子, 神保 直江, 京竹 愛子, 今川 奈央子, 吉田 美帆, 猪原 千愛, 古澤 智嗣, 尾崎 達司, 須广 佑介, 二反田 隆夫, 田中 伴典, 伊藤 智雄
    (公社)日本臨床細胞学会, Nov. 2020, 日本臨床細胞学会雑誌, 59(Suppl.2) (Suppl.2), 455 - 455, Japanese

  • 中皮腫診断におけるBAP1・MTAP等を用いた良悪判定の実際と問題点 中皮腫診断におけるBAP1・MTAPの免疫組織化学 標本作製法および染色法による影響
    塚本 龍子, 神保 直江, 京竹 愛子, 今川 奈央子, 吉田 美帆, 猪原 千愛, 古澤 智嗣, 尾崎 達司, 須广 佑介, 二反田 隆夫, 田中 伴典, 伊藤 智雄
    (公社)日本臨床細胞学会, Nov. 2020, 日本臨床細胞学会雑誌, 59(Suppl.2) (Suppl.2), 455 - 455, Japanese

  • Takashi Ogura, Ryo Okuda, Yasuhiro Kondoh, Hiroyuki Taniguchi, Takeshi Johkoh, Junya Fukuoka, Atsushi Miyamoto, Ryoko Egashira, Akira Hebisawa, Fumikazu Sakai, Tamiko Takemura, Keisuke Tomii, Kiminori Fujimoto, Tomonori Tanaka, Toru Arai, Hiromitsu Sumikawa, Takahiko Kasai, Yutaro Nakamura, Tae Iwasawa, Yasuhiro Terasaki, Takafumi Suda, Tomoyuki Fujisawa, Nobuhisa Ishikawa, Naoki Arai, Takahisa Takihara, Megumi Hamaguchi, Mikio Toyoshima, Mitsuhiro Abe, Motoyasu Kato, Hiroaki Miyata, Naoaki Ichihara, Satoshi Morita, Naohiko Inase, Hiromi Tomioka, Masashi Bandoh, Kunihiko Kobayashi, Toshihiro Nukiwa
    Sep. 2020, EUROPEAN RESPIRATORY JOURNAL, 56, English
    Summary international conference

  • 鈴木 勇三, 藤澤 朋幸, 澄川 裕充, 田中 伴典, 杉本 親寿, 安井 秀樹, 穗積 宏尚, 柄山 正人, 古橋 一樹, 榎本 紀之, 中村 祐太郎, 乾 直輝, 須田 隆文
    (一社)日本呼吸器学会, Aug. 2020, 日本呼吸器学会誌, 9(増刊) (増刊), 201 - 201, Japanese

  • 鈴木 勇三, 藤澤 朋幸, 澄川 裕充, 田中 伴典, 杉本 親寿, 安井 秀樹, 穗積 宏尚, 柄山 正人, 古橋 一樹, 榎本 紀之, 中村 祐太郎, 乾 直輝, 須田 隆文
    (一社)日本呼吸器学会, Aug. 2020, 日本呼吸器学会誌, 9(増刊) (増刊), 201 - 201, Japanese

  • 高田 尚哉, 立原 素子, 梅澤 佳乃子, 桂田 直子, 永野 達也, 山本 正嗣, 西村 善博, 大橋 千裕, 田中 雄悟, 眞庭 謙昌, 田中 伴典
    (NPO)日本肺癌学会, Apr. 2020, 肺癌, 60(2) (2), 154 - 155, Japanese

  • 嚢胞性病変を伴う肺硝子化肉芽腫の1症例(A Case of Pulmonary Hyalinizing Granulomas with Cystic Lesion)
    田中 伴典, 大谷 恭子, 酒井 康裕, 山崎 隆, 伊藤 智雄, 神保 直江
    (一社)日本病理学会, Mar. 2020, 日本病理学会会誌, 109(1) (1), 419 - 419, English

  • 田中 伴典
    (株)メジカルビュー社, Jul. 2019, 臨床画像, 35(7) (7), 830 - 835, Japanese

  • 胃異物沈着症の2例
    筑後 孝章, 大谷 知之, 田中 伴典, 榎木 英介, 前西 修, 清水 重喜, 木村 雅友, 南野 弘明, 佐藤 隆夫
    (一社)日本病理学会, Apr. 2019, 日本病理学会会誌, 108(1) (1), 367 - 367, Japanese

  • 本学の病理学教育へのWhole Slide Imaging導入の現状
    筑後 孝章, 大谷 知之, 田中 伴典, 榎木 英介, 前西 修, 清水 重喜, 木村 雅友, 佐藤 隆夫, 伊藤 彰彦
    (一社)日本病理学会, Apr. 2019, 日本病理学会会誌, 108(1) (1), 440 - 440, Japanese

  • 佐伯 翔, 西山 理, 田中 伴典, 佐野 安希子, 岩永 賢司, 東田 有智
    (一社)日本呼吸器学会, Sep. 2018, 日本呼吸器学会誌, 7(5) (5), 342 - 346, Japanese

  • 皮膚粘液癌の1例
    岡橋 一憲, 成田 智彦, 大磯 直毅, 川田 暁, 遠藤 英樹, 田中 伴典
    (公社)日本皮膚科学会, May 2018, 日本皮膚科学会雑誌, 128(6) (6), 1357 - 1357, Japanese

  • 左全肺に病変を認めたCPAMに対し待機的に左肺全摘術を施行した1例
    篠原 彰太, 山根 裕介, 銕尾 智幸, 吉田 拓哉, 田浦 康明, 小坂 太一郎, 高槻 光寿, 江口 晋, 田中 伴典, 福岡 順也, 永安 武
    (NPO)日本小児外科学会, Apr. 2018, 日本小児外科学会雑誌, 54(2) (2), 359 - 359, Japanese

  • 膵体部の膵神経内分泌腫瘍に合併した膵性胸水の一例
    河野 辰哉, 山雄 健太郎, 中井 敦史, 大本 俊介, 鎌田 研, 三長 孝輔, 宮田 剛, 今井 元, 松本 逸平, 竹山 宜典, 田中 伴典, 筑後 孝章, 林 暁洋, 工藤 正俊
    (一財)日本消化器病学会, Apr. 2018, 日本消化器病学会雑誌, 115(臨増総会) (臨増総会), A395 - A395, Japanese

  • 乳癌術後の拘束型心筋症の1剖検例
    筑後 孝章, 田中 伴典, 榎木 英介, 前西 修, 清水 重喜, 木村 雅友, 佐藤 隆夫
    (一社)日本病理学会, Apr. 2018, 日本病理学会会誌, 107(1) (1), 501 - 501, Japanese

  • 乳癌術後の拘束型心筋症の1剖検例
    筑後 孝章, 田中 伴典, 榎木 英介, 前西 修, 清水 重喜, 木村 雅友, 佐藤 隆夫
    (一社)日本病理学会, Apr. 2018, 日本病理学会会誌, 107(1) (1), 501 - 501, Japanese

  • 膵体部の膵神経内分泌腫瘍に合併した膵性胸水の一例
    河野 辰哉, 山雄 健太郎, 中井 敦史, 大本 俊介, 鎌田 研, 三長 孝輔, 宮田 剛, 今井 元, 松本 逸平, 竹山 宜典, 田中 伴典, 筑後 孝章, 林 暁洋, 工藤 正俊
    (一財)日本消化器病学会, Mar. 2018, 日本消化器病学会雑誌, 115(臨増総会) (臨増総会), A395 - A395, Japanese

  • 【間質性肺炎の診断 Up to Date】 急性・亜急性経過の間質性肺炎に対するMDD診断 病理医の立場から
    田中 伴典
    Feb. 2018, 臨床画像, 34(2) (2), 186 - 194, Japanese
    [Invited]
    Introduction scientific journal

  • MTX長期投与で発症したMTX関連リンパ増殖性疾患の1例
    佐野 安希子, 西山 理, 西川 裕作, 岩永 賢司, 東田 有智, 清水 重喜, 田中 伴典, 佐藤 隆夫
    (NPO)日本肺癌学会, Jun. 2017, 肺癌, 57(3) (3), 255 - 256, Japanese

  • 線毛性粘液結節性乳頭状腫瘍の2症例
    大坪 智恵子, 黒濱 大和, 三原 裕美, 田中 伴典, 持永 浩史, 田川 努, 藤本 俊史, 伊東 正博
    (一社)日本病理学会, Mar. 2017, 日本病理学会会誌, 106(1) (1), 372 - 372, Japanese

  • 炭酸ランタン療法中に生じた胃粘膜内ランタン沈着の経時的変化
    榎木 英介, 木村 雅友, 田中 伴典, 清水 重喜, 伊藤 彰彦, 佐藤 隆夫, 樫田 博史, 長谷川 廣文
    (一社)日本病理学会, Mar. 2017, 日本病理学会会誌, 106(1) (1), 378 - 378, Japanese

  • 肺の繊毛性粘液結節性乳頭状腫瘍を推進する変異の発見(Discovering the driver mutations in ciliated muconodular papillary tumors of the Lung)
    有働 恵美子, 古里 文吾, 坂井 和子, 今岡 由紀, 田中 伴典, 土谷 智史, 山崎 直哉, 永安 武, 西尾 和人, 福岡 順也
    (一社)日本病理学会, Mar. 2017, 日本病理学会会誌, 106(1) (1), 410 - 410, English

  • 肺大細胞がんのNGS(NGS analysis of pulmonary large cell carcinoma)
    今岡 由紀, 有働 恵美子, 古里 文吾, 坂井 和子, 田中 伴典, 土谷 智史, 山崎 直哉, 永安 武, 西尾 和人, 福岡 順也
    (一社)日本病理学会, Mar. 2017, 日本病理学会会誌, 106(1) (1), 410 - 410, English

  • 脂肪組織への進展を認め、悪性中皮腫との鑑別が問題となった胸膜Adenomatoid tumorの1例
    清水 重喜, 筑後 孝章, 武本 智樹, 田中 伴典, 榎木 英介, 前西 修, 木村 雅友, 伊藤 彰彦, 光冨 徹哉, 佐藤 隆夫
    (一社)日本病理学会, Mar. 2017, 日本病理学会会誌, 106(1) (1), 428 - 428, Japanese

  • 炭酸ランタン療法中に生じた胃粘膜内ランタン沈着の経時的変化
    榎木 英介, 木村 雅友, 田中 伴典, 清水 重喜, 伊藤 彰彦, 佐藤 隆夫, 樫田 博史, 長谷川 廣文
    (一社)日本病理学会, Mar. 2017, 日本病理学会会誌, 106(1) (1), 378 - 378, Japanese

  • 脂肪組織への進展を認め、悪性中皮腫との鑑別が問題となった胸膜Adenomatoid tumorの1例
    清水 重喜, 筑後 孝章, 武本 智樹, 田中 伴典, 榎木 英介, 前西 修, 木村 雅友, 伊藤 彰彦, 光冨 徹哉, 佐藤 隆夫
    (一社)日本病理学会, Mar. 2017, 日本病理学会会誌, 106(1) (1), 428 - 428, Japanese

  • NGS analysis of pulmonary large cell carcinoma(和訳中)
    今岡 由紀, 有働 恵美子, 古里 文吾, 坂井 和子, 田中 伴典, 土谷 智史, 山崎 直哉, 永安 武, 西尾 和人, 福岡 順也
    (一社)日本病理学会, Mar. 2017, 日本病理学会会誌, 106(1) (1), 410 - 410, English

  • Discovering the driver mutations in ciliated muconodular papillary tumors of the Lung(和訳中)
    有働 恵美子, 古里 文吾, 坂井 和子, 今岡 由紀, 田中 伴典, 土谷 智史, 山崎 直哉, 永安 武, 西尾 和人, 福岡 順也
    (一社)日本病理学会, Mar. 2017, 日本病理学会会誌, 106(1) (1), 410 - 410, English

  • 陰嚢内及び後腹膜に進展する脱分化型脂肪肉腫の1例
    藤江 祥子, 山口 哲治, 小池 玄文, 上谷 雅孝, 計屋 知彰, 志田 洋平, 酒井 英樹, 田中 伴典, 新野 大介, 福岡 順也
    (公社)日本医学放射線学会, Feb. 2017, Japanese Journal of Radiology, 35(Suppl.) (Suppl.), 89 - 89, Japanese

  • 【間質性肺炎のMDD(multi-disciplinary discussion)】 病理医からみた間質性肺炎のMDD診断
    田中 伴典, 福岡 順也
    医歯薬出版(株), Feb. 2017, 医学のあゆみ, 260(8) (8), 653 - 656, Japanese
    [Invited]

  • 新田 哲久, 田中 伴典, 園田 明永, 大谷 秀司, 永谷 幸裕, 村田 喜代史, 高橋 雅士, 福岡 順也
    (株)学研メディカル秀潤社, Jun. 2016, 画像診断, 36(8) (8), 754 - 766, Japanese

  • 子宮粘膜下筋腫あるいは内膜ポリープの診断で子宮鏡下手術を行い、術後に子宮内膜癌と診断した5例
    荒木 裕之, 妹尾 悠, 北島 百合子, 吉武 朋子, 平木 宏一, 藤下 晃, 荻野 歩, 津田 暢夫, 田中 伴典, 河合 紀生子, 岸川 正大
    (公社)日本婦人科腫瘍学会, Jun. 2016, 日本婦人科腫瘍学会雑誌, 34(3) (3), 427 - 427, Japanese

  • 2011年ATS/ERS/JRS/ALATのIPFガイドラインを用いた診断一致率の検討(Inter-Observer Agreement of Usual Interstitial Pneumonia Diagnosis Correlated with Patient Outcome)
    橋迫 美貴子, 田中 伴典, 田畑 和宏, 植草 利公, 寺崎 泰弘, 林 徳真吉, 谷口 博之, 近藤 康博, 片岡 健介, 福岡 順也
    (一社)日本病理学会, Apr. 2016, 日本病理学会会誌, 105(1) (1), 355 - 355, English

  • 中枢神経原発リンパ腫におけるPD-1発現の検討(Programmed cell death-1(PD-1) expression in primary central nervous system lymphoma(PCNSL))
    安井 春奈, 新野 大介, 出端 亜由美, 橋迫 美貴子, 田中 伴典, 田畑 和宏, 木下 直江, 古里 文吾, 安倍 邦子, 福岡 順也
    (一社)日本病理学会, Apr. 2016, 日本病理学会会誌, 105(1) (1), 357 - 357, English

  • 生検試料の病理学的診断のための全スライド画像の検証(Validation of Whole slide imaging for pathological diagnosis in biopsy specimen)
    田畑 和宏, 橋迫 美貴子, 田中 伴典, 安井 春奈, 木下 直江, 古里 文吾, 新野 大介, 安倍 邦子, 福岡 順也
    (一社)日本病理学会, Apr. 2016, 日本病理学会会誌, 105(1) (1), 371 - 371, English

  • 急性線維素性器質化肺炎とランゲルハンス細胞組織球増殖症が併発した1症例(A case of combined acute fibrinous and organizing pneumonia and Langerhans cell histiocytosis)
    石田 佳央理, 田中 伴典, 橋迫 美貴子, Groen Ruben, 角川 智之, 原 敦子, 坂本 憲穂, 福岡 順也
    (一社)日本病理学会, Apr. 2016, 日本病理学会会誌, 105(1) (1), 388 - 389, English

  • 成人T細胞白血病・リンパ腫(ATLL)におけるPD-1の発現(The expression of Programmed death-1(PD-1) in Adult T-cell leukemia/lymphoma(ATLL))
    有働 恵美子, 新野 大介, 橋迫 美貴子, 田中 伴典, 田畑 和宏, 木下 直江, 古里 文吾, 安倍 邦子, 福岡 順也
    (一社)日本病理学会, Apr. 2016, 日本病理学会会誌, 105(1) (1), 499 - 499, English

  • 扁平上皮化生 通常型間質性肺炎における急性増悪の組織学的特徴と予後不良因子(Squamous metaplasia: Factor of acute exacerbation and poor prognosis in usual interstitial pneumonia)
    原 正武, 橋迫 美貴子, 山野 泰彦, 田中 伴典, 田畑 和宏, 上甲 剛, 近藤 康博, 谷口 博之, 福岡 順也
    (一社)日本病理学会, Apr. 2016, 日本病理学会会誌, 105(1) (1), 585 - 585, English

  • 肺腺癌の微小乳頭構造とspread through air space(STAS)に関する3D組織学的分析(Micropapillary structure of lung adenocarcinoma and spread through air space(STAS) in 3D histology)
    吉川 亮, つる野 広介, 田中 伴典, 田畑 和宏, 土屋 智史, 山崎 直哉, 永安 武, 芦澤 和人, 福岡 順也
    (一社)日本病理学会, Apr. 2016, 日本病理学会会誌, 105(1) (1), 589 - 589, English

  • CTで発見された肺結節の判定基準と経過観察 長崎県における多施設共同研究
    森 雅一, 北崎 健, 福島 喜代康, 吉田 伸太郎, 近藤 晃, 筒井 伸, 福田 俊夫, 福島 文, 吉岡 寿麻子, 高谷 洋, 荻原 幸宏, 中村 洋一, 森本 浩之輔, 山崎 直哉, 田中 伴典, 林 秀行, 福田 実, 芦澤 和人
    (NPO)日本CT検診学会, Feb. 2016, CT検診, 23(1) (1), 16 - 16, Japanese

  • 肝血管筋脂肪腫の1例
    柴田 英貴, 原口 雅史, 三馬 聡, 森 智崇, 本田 琢也, 宮明 寿光, 田中 伴典, 角田 順久, 田浦 直太, 中尾 一彦
    (公社)日本超音波医学会, Jan. 2016, 超音波医学, 43(1) (1), 163 - 164, Japanese

  • 上肺優位の間質性肺炎症例の検討
    近藤康博, 谷口博之, 木村智樹, 片岡健介, 山野泰彦, 古川大記, 櫻井あや, 福岡順也, 田中伴典, 上甲剛
    2016, 間質性肺疾患研究会討議録, 90th

  • 西牟田 雅人, 山崎 直哉, 小畑 智裕, 渡邊 洋之助, 北村 由香, 畑地 豪, 宮崎 拓郎, 松本 桂太郎, 土谷 智史, 田中 伴典, 田畑 和宏, 永安 武
    日本臨床外科学会, Oct. 2015, 日本臨床外科学会雑誌, 76(増刊) (増刊), 797 - 797, Japanese

  • 呼吸困難で術前に気管挿管を要した巨大バセドウ氏病の1例
    矢野 洋, 松本 恵, 大坪 竜太, 進藤 久和, 福嶋 絢子, 新野 大介, 田中 伴典, 永安 武
    日本内分泌外科学会・日本甲状腺外科学会, Sep. 2015, 日本内分泌・甲状腺外科学会雑誌, 32(Suppl.2) (Suppl.2), S273 - S273, Japanese

  • NBI併用拡大内視鏡観察にて観察し得た肝門部十二指腸球部吻合術後胆管に発症した早期胆管癌の1例
    庄司 寛之, 大仁田 賢, 原口 雅史, 高原 郁子, 中鋪 卓, 磯本 一, 田畑 和宏, 田中 伴典, 安倍 邦子, 福岡 順也, 中尾 一彦
    日本胆道学会, Aug. 2015, 胆道, 29(3) (3), 653 - 653, Japanese

  • 4ヵ月間で急速に増大した後腹膜奇形腫の1例
    大石 海道, 田浦 康明, 大畠 雅之, 山根 裕介, 小坂 太一郎, 江口 晋, 田中 伴典, 木下 直江, 福岡 順也, 永安 武
    (一社)日本小児血液・がん学会, Aug. 2015, 日本小児血液・がん学会雑誌, 52(2) (2), 193 - 193, Japanese

  • 乳腺線維腺腫に隣接した粗大石灰化を伴う粘液癌の一例
    馬場 雅之, 大坪 竜太, 榊原 優香, 畑地 登志子, 進藤 久和, 松本 恵, 田中 伴典, 木下 直江, 矢野 洋, 福岡 順也, 永安 武
    (一社)日本乳癌学会, Jul. 2015, 日本乳癌学会総会プログラム抄録集, 23回, 704 - 704, Japanese

  • FDG-PET/CTが転移性脊椎腫瘍とSAPHO症候群の鑑別に有用であった一例
    小武 隆子, 上谷 雅孝, 井手口 怜子, 工藤 崇, 田中 伴典
    (一社)日本核医学会, May 2015, 核医学, 52(2) (2), 76 - 76, Japanese

  • 櫻井 あや, 谷口 博之, 近藤 康博, 木村 智樹, 片岡 健介, 松田 俊明, 横山 俊樹, 古川 大記, 上甲 剛, 澄川 裕充, 福岡 順也, 田中 伴典
    (一社)日本呼吸器学会, Mar. 2015, 日本呼吸器学会誌, 4(増刊) (増刊), 163 - 163, Japanese

  • 顕微鏡的蜂巣肺の診断一致率及び臨床的意義の検討(Interobserver agreement and clinical meaning of microscopic honeycomb in the cases of IPF)
    田畑 和宏, 矢田 秀雄, 田中 伴典, 加島 志郎, 橋迫 美貴子, 上甲 剛, 片岡 健介, 近藤 康博, 谷口 博之, 福岡 順也
    (一社)日本病理学会, Mar. 2015, 日本病理学会会誌, 104(1) (1), 311 - 311, English

  • 瘢痕性の器質性肺炎の臨床的、放射線学的、および病理学的特徴(Clinical-radiological-pathological features of scarring organizing pneumonia)
    橋迫 美貴子, 田中 伴典, 加島 志郎, 田畑 和宏, 上甲 剛, 片岡 健介, 近藤 康博, 谷口 博之, Moran Cecar A, 福岡 順也
    (一社)日本病理学会, Mar. 2015, 日本病理学会会誌, 104(1) (1), 311 - 311, English

  • 三次元の病理学的な画像再構成から明らかになった肺の最小ユニットと肺気腫の初期イベント(3D pathology construction reveals the minimal unit of the lung and the initial event of emphysema)
    吉川 亮, 田中 伴典, 橋迫 美貴子, 加島 志郎, 唐田 博貴, 田畑 和宏, 福岡 順也
    (一社)日本病理学会, Mar. 2015, 日本病理学会会誌, 104(1) (1), 511 - 511, English

  • 慢性過敏性肺炎の特異的病理学的所見の同定(Identification of Specific Histopayhological Findings in Chronic Hypersensitivity Pneumonitis)
    市川 宏美, 大力 睦, 田中 伴典, 谷口 博之, 上甲 剛, 片岡 健介, 近藤 康博, 福岡 順也
    (一社)日本病理学会, Mar. 2015, 日本病理学会会誌, 104(1) (1), 512 - 512, English

  • 特発性間質性肺炎と膠原病関連性間質性肺炎の病理組織学的鑑別診断(Histological Findings Specific for Connective Tissue Disease Associated Interstitial Pneumonia)
    大力 睦, 市川 宏美, 田中 伴典, 谷口 博之, 上甲 剛, 片岡 健介, 近藤 康博, 福岡 順也
    (一社)日本病理学会, Mar. 2015, 日本病理学会会誌, 104(1) (1), 512 - 512, English

  • 3D Pathology Construction Reveals Framework Structure of the Lung and Increase of Pores of Kohn as an Initial Event of Emphysema
    Akira Yoshikawa, Tomonori Tanaka, Mikiko Hashisako, Yukio Kashima, Hiroki Karata, Kazuhiro Tabata, Junya Fukuoka
    Feb. 2015, LABORATORY INVESTIGATION, 95, 493A - 494A, English
    Summary international conference

  • 3D Pathology Construction Reveals Framework Structure of the Lung and Increase of Pores of Kohn as an Initial Event of Emphysema
    Akira Yoshikawa, Tomonori Tanaka, Mikiko Hashisako, Yukio Kashima, Hiroki Karata, Kazuhiro Tabata, Junya Fukuoka
    Feb. 2015, MODERN PATHOLOGY, 28, 493A - 494A, English
    Summary international conference

  • Histological Difference Between Idiopathic Interstitial Pneumonias and Connective Tissue Disease-Associated Interstitial Pneumonias
    Minsumi Dairiki, Hiromi Ichikawa, Tomonori Tanaka, Hiroyuki Taniguchi, Takeshi Johkoh, Kensuke Kataoka, Yasuhiro Kondoh, Junya Fukuoka
    Feb. 2015, LABORATORY INVESTIGATION, 95, 475A - 475A, English
    Summary international conference

  • Histological Difference Between Idiopathic Interstitial Pneumonias and Connective Tissue Disease-Associated Interstitial Pneumonias
    Mutsumi Dairiki, Hiromi Ichikawa, Tomonori Tanaka, Hiroyuki Taniguchi, Takeshi Johkoh, Kensuke Kataoka, Yasuhiro Kondoh, Junya Fukuoka
    Feb. 2015, MODERN PATHOLOGY, 28, 475A - 475A, English
    Summary international conference

  • 胸腺原発MALTリンパ腫の1切除例
    谷口大輔, 山崎直哉, 土谷智史, 松本桂太郎, 宮崎拓郎, 田中伴典, 田畑和宏, 永安武
    2015, 日本胸腺研究会プログラム・抄録集, 34th

  • びまん性肺疾患に関する調査研究班 2011年ATS/ERS/JRS/ALATのIPFガイドラインにおける病理診断一致率の検討
    福岡順也, 福岡順也, 植草利公, 寺崎泰弘, 田中伴典, 田畑和宏, 橋迫美貴子, 谷口博之, 近藤康博, 片岡健介
    2015, びまん性肺疾患に関する調査研究 平成26年度 研究報告書, 103‐108, Japanese

  • 肺癌背景肺におけるMuc5B発現
    高畑 海音子, 橋迫 美貴子, 田中 伴典, 田畑 和宏, 加島 志郎, 山崎 直哉, 土谷 智史, 松本 桂太郎, 宮崎 拓郎, 永安 武, 福岡 順也
    (NPO)日本肺癌学会, Oct. 2014, 肺癌, 54(5) (5), 433 - 433, Japanese

  • 肺グロームス腫瘍の1例
    森 美央, 林 秀行, 荻原 幸宏, 上谷 雅孝, 西田 暁史, 芦澤 和人, 山崎 直哉, 永安 武, 田中 伴典, 福岡 順也
    (公社)日本医学放射線学会, Sep. 2014, 日本医学放射線学会秋季臨床大会抄録集, 50回, S707 - S708, Japanese

  • 多発結節影を呈したCaplan症候群の1例
    荻原 幸宏, 芦澤 和人, 林 秀行, 川上 純, 山崎 直哉, 永安 武, 田中 伴典, 田畑 和宏, 福岡 順也, 上谷 雅孝
    (公社)日本医学放射線学会, Sep. 2014, 日本医学放射線学会秋季臨床大会抄録集, 50回, S714 - S714, Japanese

  • 濱邊 順平, 立石 洋平, 辻野 彰, 久富 一輝, 松隈 誠司, 谷川 和好, 江石 清行, 恒任 章, 前村 浩二, 中山 敏幸, 田中 伴典, 林 徳真吉, 福岡 順也
    (一社)日本神経学会, Jun. 2014, 臨床神経学, 54(6) (6), 528 - 528, Japanese

  • 町野 隆介, 山崎 直哉, 宮崎 拓郎, 松本 桂太郎, 土谷 智史, 田中 伴典, 永安 武
    (NPO)日本呼吸器内視鏡学会, May 2014, 気管支学, 36(3) (3), 319 - 319, Japanese

  • 新田 哲久, 高橋 雅士, 園田 明永, 大谷 秀司, 永谷 幸裕, 村田 喜代史, 田中 伴典, 福岡 順也
    (株)学研メディカル秀潤社, May 2014, 画像診断, 34(7) (7), 786 - 797, Japanese

  • 甲状腺の腺腫様結節と濾胞性腫瘍における細胞学的鑑別因子の同定研究
    堀 隆, 布村 さゆり, 田中 伴典, 福岡 順也, 小梶 恵利, 野本 一博
    (公社)日本臨床細胞学会, Apr. 2014, 日本臨床細胞学会雑誌, 53(Suppl.1) (Suppl.1), 215 - 215, Japanese

  • 肺門部Glomus腫瘍の1例
    町野 隆介, 山崎 直哉, 宮崎 拓郎, 松本 桂太郎, 土谷 智史, 永安 武, 田中 伴典
    (NPO)日本肺癌学会, Apr. 2014, 肺癌, 54(2) (2), 108 - 109, Japanese

  • P-index UIP患者における予後予測のための簡易で有効な組織学的ツール(P-index: A Simple and Validated Histological Tool for Predicting Prognosis in UIP patients)
    岡村 岳, 田中 伴典, 加島 志郎, 田畑 和宏, 林 健太郎, 鶴野 広介, 片岡 健介, 近藤 康博, 谷口 博之, 渡辺 憲太朗, 原田 泰志, 福岡 順也
    (一社)日本病理学会, Mar. 2014, 日本病理学会会誌, 103(1) (1), 205 - 205, English

  • 弾力線維症によるperilobular margination 通常型間質性肺炎の堅牢な組織学的マーカ(Perilobular Margination by Elastosis: A Robust Histologic Marker of Usual Interstitial Pneumonia)
    牛草 健, 田畑 和宏, 田中 伴典, 鶴野 広介, 峠田 直人, 加島 志郎, 片岡 健介, 近藤 康博, 谷口 博之, 福岡 順也
    (一社)日本病理学会, Mar. 2014, 日本病理学会会誌, 103(1) (1), 206 - 206, English

  • 肺門部Glomus腫瘍の1例
    町野隆介, 山崎直哉, 宮崎拓郎, 松本桂太郎, 土谷智史, 永安武, 田中伴典
    2014, 肺癌(Web), 54(2) (2)

  • 田中 伴典
    日本サルコイドーシス, Oct. 2013, 日本サルコイドーシス/肉芽腫性疾患学会雑誌, 33(1-2) (1-2), 23 - 26, Japanese
    [Invited]

  • 尿細胞診で診断された膀胱原発悪性黒色腫の一例
    堀 隆, 布村 さゆり, 木屋 千恵子, 野本 一博, 田中 伴典, 福岡 順也
    (公社)日本臨床細胞学会, May 2013, 日本臨床細胞学会雑誌, 52(Suppl.1) (Suppl.1), 226 - 226, Japanese

  • 病理診断標準化を目的としたウェブフリー診断補助ソフトの構築 肺線維症の場合
    田中 伴典, 林 徳真吉, 田畑 和宏, 加島 志郎, 布村 さゆり, 安井 春奈, 木下 直江, 安倍 邦子, 中山 敏幸, 片岡 健介, 近藤 康博, 谷口 博之, 福岡 順也
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 317 - 317, Japanese

  • 筋上皮成分の小壊死巣や高い増殖能を示す腺筋上皮腫の一例
    安倍 邦子, 林 徳真吉, 木下 直江, 安井 春奈, 田中 伴典, 中山 敏幸, 矢野 洋, 及川 将弘, 松本 恵, 永安 武, 森谷 卓也, 福岡 順也
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 370 - 370, Japanese

  • 早期食道癌におけるリン酸化eIF4E発現の検討
    中山 敏幸, 嶋倉 茜, 南 ひとみ, 山口 直之, 磯本 一, 安井 春奈, 田中 伴典, 安倍 邦子, 中尾 一彦, 福岡 順也, 林 徳眞吉
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 383 - 383, Japanese

  • 再発を来した脊髄神経の混成シュワン細胞腫・神経周膜腫
    林 徳真吉, 安倍 邦子, 木下 直江, 安井 春奈, 田中 伴典, 中山 敏幸, 福岡 順也, 西村 行政, 廣瀬 隆則, 岸川 正大
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 394 - 394, Japanese

  • 上皮内成分を確認できず診断に苦慮した腎の形質細胞様型浸潤性尿路上皮癌の1例
    木下 直江, 林 徳真吉, 安倍 邦子, 中山 敏幸, 安井 春奈, 田中 伴典, 酒井 英樹, 宮田 康好, 大庭 康司郎, 鹿子木 桂, 杠葉 美樹, 浅井 昭宏, 福岡 順也
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 410 - 410, Japanese

  • 高齢者に偶発的に発見された腎mixed epithelial and stromal tumorの一例
    杉口 俊, 寺畑 信太郎, 田中 伴典
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 410 - 410, Japanese

  • 肺胞蛋白症様変化は特発性肺線維症で一般的な反応である(Pulmonary Alveolar Proteinosis Like Change Is a Common Reaction in Idiopathic Pulmonary Fibrosis)
    布村 さゆり, 田中 伴典, 大谷 恭子, 田畑 和宏, 中山 敏幸, 林 徳真吉, 近藤 康博, 片岡 健介, 上甲 剛, 谷口 博之, 福岡 順也
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 423 - 423, English

  • 肺線維症におけるProSP-Cの発現量低下は病態の進行を示す組織学的な指標である(Lower expression of ProSP-C in pulmonary fibrosis As a Histological Marker of Disease progression)
    布村 さゆり, 田畑 和宏, 田中 伴典, 堀 隆, 加島 志郎, 林 徳真吉, 中山 敏幸, 福岡 順也
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 424 - 424, English

  • 肺気腫と喫煙の肺線維症との関連性(Association of emphysema and Tobacco smoking with pulmonary fibrosis)
    田畑 和宏, 田中 伴典, 大谷 恭子, 布村 さゆり, 片岡 健介, 近藤 康博, 上甲 剛, 谷口 博之, 福岡 順也
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 424 - 424, Japanese

  • Ciliated muconodular papillary tumor of the lungの免疫組織化学的検討
    安井 春奈, 林 徳真吉, 田中 伴典, 木下 直江, 安倍 邦子, 中山 敏幸, 山崎 直哉, 永安 武, 福岡 順也
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 425 - 425, Japanese

  • 肺病変先行型結合組織疾患の病理学的特徴(Pathological features of lung dominant connective tissue disease)
    大谷 恭子, 田中 伴典, 表 紀仁, 片岡 健介, 近藤 康博, 谷口 博之, 田畑 和宏, 福岡 順也, 伊藤 智雄
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 425 - 425, Japanese

  • 間質性肺疾患における細気管支周囲異形成の有病率(Prevalence of Peribronchiolar Metaplasia In The Interstitial Lung Disease)
    林 亮佑, 田中 伴典, 田畑 和宏, 大谷 恭子, 加島 志郎, 布村 さゆり, 片岡 健介, 近藤 康博, 谷口 博之, 福岡 順也
    (一社)日本病理学会, Apr. 2013, 日本病理学会会誌, 102(1) (1), 498 - 498, English

  • 疾患と運動時低酸素血症 運動時低酸素血症を来す疾患の病理診断
    福岡 順也, 田畑 和宏, 田中 伴典, 林 徳真吉
    (一社)日本呼吸器学会, Mar. 2013, 日本呼吸器学会誌, 2(増刊) (増刊), 28 - 28, Japanese

  • Neurolymphomatosisの1例
    鳴戸 規人, 神前 裕一, 富澤 岳人, 亀田 圭介, 川部 秀人, 森尻 実, 加藤 洋, 野口 京, 瀬戸 光, 田中 伴典, 三輪 重治
    (公社)日本医学放射線学会, Feb. 2013, Japanese Journal of Radiology, 31(Suppl.I) (Suppl.I), 41 - 41, Japanese

  • 喫煙者における線維化を伴う肺気腫とIPFの比較評価
    大谷 秀司, 村田 喜代史, 新田 哲久, 永谷 幸裕, 高橋 雅士, 福岡 順也, 田中 伴典
    (公社)日本医学放射線学会, Feb. 2013, 日本医学放射線学会学術集会抄録集, 72回, S212 - S212, Japanese

  • 気道狭窄を来した扁平上皮癌の1例
    徳井 宏太郎, 市川 智巳, 津田 岳志, 岡澤 成祐, 神原 健太, 今西 信悟, 山田 徹, 三輪 敏郎, 林 龍二, 戸邉 一之, 仙田 一貴, 土岐 善紀, 安藤 孝将, 松井 祥子, 菓子井 達彦, 田中 伴典, 福岡 順也, 岩田 安弘
    (NPO)日本肺癌学会, Oct. 2012, 肺癌, 52(6) (6), 987 - 987, Japanese

  • 前縦隔悪性腫瘍の1例
    今西 信悟, 鈴木 健介, 津田 岳志, 徳井 宏太郎, 岡澤 成祐, 神原 健太, 山田 徹, 三輪 敏郎, 林 龍二, 戸辺 一之, 松井 祥子, 石井 陽子, 笹原 正清, 菓子井 達彦, 田中 伴典, 福岡 順也
    (NPO)日本肺癌学会, Oct. 2012, 肺癌, 52(6) (6), 988 - 988, Japanese

  • サルコイドーシス/肉芽腫性肺疾患の画像・病理・呼吸機能 サルコイドーシス・肉芽腫性肺疾患の病理
    田中 伴典, 福岡 順也
    日本サルコイドーシス, Sep. 2012, 日本サルコイドーシス/肉芽腫性疾患学会雑誌, 32(サプリメント号) (サプリメント号), 19 - 19, Japanese

  • 医療の現場に役立つデジタルパソロジー 病理診断標準化を目的としたウェブフリー診断補助ソフトの構築 間質性肺炎における試み
    福岡 順也, 田畑 和宏, 田中 伴典, 加島 志郎, 布村 さゆり
    (一社)日本病理学会, Sep. 2012, 日本病理学会会誌, 101(2) (2), 28 - 28, Japanese

  • 肺癌を合併した喫煙関連肺疾患の1剖検例
    垣内 寿枝子, 田畑 和宏, 田中 伴典, 大谷 恭子, 加島 志郎, 福岡 順也
    (一社)日本病理学会, Sep. 2012, 日本病理学会会誌, 101(2) (2), 51 - 51, Japanese

  • 林 龍二, 池田 理栄, 津田 岳志, 下川 一生, 岡澤 成祐, 神原 健太, 猪又 峰彦, 今西 信悟, 市川 智巳, 鈴木 健介, 山田 徹, 三輪田 敏郎, 戸邊 一之, 松井 祥子, 田中 伴典, 福岡 順也
    (NPO)日本呼吸器内視鏡学会, Jul. 2012, 気管支学, 34(4) (4), 407 - 408, Japanese

  • 抗IL-6受容体抗体治療中に肺アスペルギルス症が出現した関節リウマチの一例
    下川 一生, 市川 智巳, 鈴木 健介, 今西 信悟, 山田 徹, 篠田 晃一郎, 林 龍二, 多喜 博文, 戸邉 一之, 松下 功, 福岡 順也, 田中 伴典, 土岐 善紀, 仙田 一貴, 本間 崇浩
    (一社)日本呼吸器学会, Mar. 2012, 日本呼吸器学会誌, 1(増刊) (増刊), 290 - 290, Japanese

  • スパイラルアレイは肺癌の生存解析における組織不均一性をカバーする(Spiral Array Covers Tissue Heterogeneity for Survival Analysis of Lung Cancer)
    福岡 順也, 堀 隆, 田中 伴典, 布村 さゆり
    (一社)日本病理学会, Mar. 2012, 日本病理学会会誌, 101(1) (1), 257 - 257, English

  • 非特異的間質性肺炎の急速進行例 独特な症例なのか?(Rapidly progressing cases of Nonspecific Interstitial Pneumonia: Are they unique?)
    田中 伴典, 大谷 恭子, 垣内 寿枝子, 布村 さゆり, 福岡 順也
    (一社)日本病理学会, Mar. 2012, 日本病理学会会誌, 101(1) (1), 279 - 279, English

  • 肉芽腫と巨細胞を有する通常型間質性肺炎 臨床病理学的特徴(Usual Interstitial Pneumonia with Granuloma and Giant Cells: Clinicopathological Features)
    大谷 恭子, 田中 伴典, 布村 さゆり, 垣内 寿枝子, 福岡 順也
    (一社)日本病理学会, Mar. 2012, 日本病理学会会誌, 101(1) (1), 393 - 393, English

  • 病理用スパイラルアレイのWhole Block、CNB、高密度アレイへの応用(Application of the Spiral Array for Pathology, to use of Whole Block, CNB, and High-Density Array)
    堀 隆, 田中 伴典, 布村 さゆり, 福岡 順也
    (一社)日本病理学会, Mar. 2012, 日本病理学会会誌, 101(1) (1), 429 - 429, Japanese

  • 肺の中枢型扁平上皮癌と末梢型扁平上皮癌の比較(Comparison of Central vs. Peripheral Squamous Cell Carcinoma of the Lung)
    佐野 寿郎, 田中 伴典, 福岡 順也
    (一社)日本病理学会, Mar. 2012, 日本病理学会会誌, 101(1) (1), 437 - 437, English

  • 自然気胸内に隠れた小さな気道疾患(Small Airway Disease Hidden Inside Spontaneous Pneumothorax)
    垣内 寿枝子, 田中 伴典, 大谷 恭子, 福岡 順也
    (一社)日本病理学会, Mar. 2012, 日本病理学会会誌, 101(1) (1), 440 - 440, English

  • 弾性線維症は慢性間質性肺炎における組織学的予後因子か?(An Elastosis Is a Histologic Prognostic Factor in Chronic Interstitial Pneumonia)
    峠田 直人, 田中 伴典, 大谷 恭子, 福岡 順也
    (一社)日本病理学会, Mar. 2012, 日本病理学会会誌, 101(1) (1), 440 - 440, English

  • 卵巣の「微小乳頭状パターンを伴う漿液性境界悪性腫瘍」の一例
    堀 隆, 石井 陽子, 田中 伴典, 野本 一博, 布村 さゆり, 福岡 順也
    (公社)日本臨床細胞学会, Mar. 2012, 日本臨床細胞学会雑誌, 51(Suppl.1) (Suppl.1), 379 - 379, Japanese

  • スパイラルアレイによる肺がんの予後検討 Ki67について(Application of Spiral Array to Survival Analysis of Lung Cancer: Tissue Heterogeneity of Ki67 Matters)
    田中 伴典, 福岡 順也, 堀 隆
    日本毒性病理学会, Feb. 2012, 日本毒性病理学会講演要旨集, 28回, 83 - 83, English

  • 堀 隆, 田中 伴典, 福岡 順也
    (株)医学書院, Nov. 2011, 検査と技術, 39(12) (12), 1115 - 1118, Japanese

  • びまん性肺疾患 研究と診療の新たな展開 びまん性肺疾患の病理診断
    福岡 順也, 田中 伴典, 富永 正樹
    日本医学会, Oct. 2011, 日本医学会総会会誌, 28回(I) (I), 205 - 205, Japanese

  • 呼吸器細胞診TECHNO-COLLEGE LBC標本を用いたカクテル抗体免疫染色による肺癌組織型診断の検討
    堀 隆, 布村 さゆり, 浜田 桂司, 田中 伴典, 福岡 順也
    (公社)日本臨床細胞学会, Sep. 2011, 日本臨床細胞学会雑誌, 50(Suppl.2) (Suppl.2), 476 - 476, Japanese

  • 【特発性肺線維症(IPF)】 特発性肺線維症(IPF)の病理診断
    福岡 順也, 田中 伴典, 大谷 恭子
    (有)科学評論社, Jun. 2011, 呼吸器内科, 19(6) (6), 533 - 539, Japanese

  • 【びまん性肺疾患 これだけは押さえておきたいHRCT診断の基本】 びまん性肺疾患のHRCT 嚢胞性病変(低吸収性病変)の基本
    新田 哲久, 田中 伴典, 園田 明永, 大谷 秀司, 永谷 幸裕, 高橋 雅士, 村田 喜代史, 福岡 順也
    (株)メジカルビュー社, Apr. 2011, 臨床画像, 27(4) (4), 477 - 492, Japanese

  • 形態保持能が改善した新規ハイスループット法としてのスパイラルアレイ法(Spiral Array Is a Nobel High-Throughput Technique Keeping Better Morphology)
    福岡 順也, 堀 隆, 斉当 愛美, 石澤 伸, 野本 一博, 田中 伴典, 加島 志郎
    (一社)日本病理学会, Mar. 2011, 日本病理学会会誌, 100(1) (1), 358 - 358, English

  • 乳癌患者のコア針生検標本中のバイオマーカーを検査するためのspiral array(Spiral Array to test biomarkers in Core Needle Biopsy from Breast Cancer Patients)
    堀 隆, 田中 伴典, 福岡 順也
    (一社)日本病理学会, Mar. 2011, 日本病理学会会誌, 100(1) (1), 397 - 397, English

  • NSIPにおける病理組織所見に対応したBAL所見(BAL Findings Corresponding to Histopathology in NSIP)
    斉当 愛実, 田中 伴典, 富永 正樹, 加島 志郎, 片岡 健介, 近藤 康博, 谷口 博之, 福岡 順也
    (一社)日本病理学会, Mar. 2011, 日本病理学会会誌, 100(1) (1), 501 - 501, English

  • 抗NMDA受容体抗体関連脳症を合併した小細胞肺癌の1例
    下川 一生, 正木 康晶, 岡沢 成祐, 神原 健太, 今西 信吾, 市川 智巳, 猪又 峰彦, 山田 徹, 鈴木 健介, 三輪 敏郎, 林 龍二, 戸邉 一之, 松井 祥子, 菓子井 達彦, 八野田 純, 安田 剛敏, 温井 孝昌, 田口 芳治, 田中 伴典, 三輪 重治, 常山 幸一, 高野 志保, 森 寿
    (NPO)日本肺癌学会, Feb. 2011, 肺癌, 51(1) (1), 47 - 48, Japanese

  • PATHOLOGICAL CLASSIFICATION OF INTERSTITIAL LUNG DISEASE
    Junya Fukuoka, Tomonori Tanaka, Manami Saito, Masaki Tominaga, Shigeki Shimizu
    Nov. 2010, RESPIROLOGY, 15, 10 - 10, English
    Summary international conference

  • 画像診断 びまん性肺疾患の画像診断のこつ のう胞性陰影
    新田 哲久, 田中 伴典, 園田 明永, 大谷 秀司, 永谷 幸裕, 高橋 雅士, 村田 喜代史, 福岡 順也
    (一社)呼吸研究, Apr. 2010, 呼吸, 29(4) (4), 377 - 390, Japanese

  • 集学的治療により救命しえた劇症型A群連鎖球菌感染症の2例
    下川 一生, 有嶋 拓郎, 旭 雄士, 若杉 雅浩, 田中 伴典, 工廣 紀斗司, 奥寺 敬
    富山救急医療学会, Aug. 2009, 富山救急医療研究会, 27回, 10 - 10, Japanese

  • 急速進行性の間質性肺炎の病態をめぐって 急速進行性の間質性肺炎と病理
    福岡 順也, 江頭 玲子, 田中 伴典
    (一社)日本呼吸器学会, May 2009, 日本呼吸器学会雑誌, 47(増刊) (増刊), 34 - 34, Japanese

  • 【呼吸器症候群(第2版) その他の呼吸器疾患を含めて】 腫瘍性疾患 上皮性(原発性)腫瘍 乳頭腫
    岩田 安弘, 江頭 玲子, 田中 伴典, 福岡 順也
    (株)日本臨床社, Mar. 2009, 日本臨床, 別冊(呼吸器症候群III) (呼吸器症候群III), 60 - 64, Japanese

  • バイオインフォマティクスと組織アレイを用いた予後・治療効果予測因子の探索
    影山 俊一郎, 飯沼 ゆり子, 田中 伴典, 江頭 玲子, 鈴木 賀代, 加島 志郎, 丸野 崇志, 福岡 順也
    (一社)日本病理学会, Mar. 2009, 日本病理学会会誌, 98(1) (1), 399 - 399, Japanese

  • 福岡 順也, 鈴木 健介, 田中 伴典, 影山 俊一郎, 堀 隆
    (NPO)日本呼吸器内視鏡学会, May 2008, 気管支学, 30(Suppl.) (Suppl.), S102 - S102, Japanese

  • 肺癌研究における新たなエンティティとテクノロジー 高集積組織アレイ研究から試みる肺癌の個別化医療
    福岡 順也, 田中 伴典, 北野 晴久, 堀 隆, 坂井 祐太, 釜谷 寛之, 影山 俊一郎, 野本 一博
    (一社)日本病理学会, Mar. 2008, 日本病理学会会誌, 97(1) (1), 158 - 158, Japanese

  • HTLV-1キャリアにおける瀰漫性肺粟粒病変の3症例:HABA非定型の提唱(Three cases of diffuse pulmonary miliary lesions in HTLV-1 careers: Proposed variant of "HABA")
    田中 伴典, 一門 和哉, 菅 守隆, 堀 隆, 石澤 伸, 福岡 順也
    (一社)日本病理学会, Mar. 2008, 日本病理学会会誌, 97(1) (1), 390 - 390, English

  • 肺癌患者の救済療法薬としての細胞質JAB1(Cytoplasmic JAB1 act as rescuer in the patients with lung cancer)
    影山 俊一郎, 釜谷 寛之, 北野 晴久, 田中 伴典, 坂井 祐太, 堀 隆, 福岡 順也
    (一社)日本病理学会, Mar. 2008, 日本病理学会会誌, 97(1) (1), 393 - 393, English

  • 広汎な筋線維芽細胞の増殖を伴う胎盤性"血管腫"(Placental "hemangioma" with an extensive myofibroblastic proliferation)
    夏目 岳典, 仁井見 英樹, 田中 伴典, 中村 隆文, 福永 真治, 野島 孝之, 中嶋 安彬, 南口 早智子, 石井 陽子, 塩崎 有宏, 斉藤 滋, 福岡 順也
    (一社)日本病理学会, Mar. 2008, 日本病理学会会誌, 97(1) (1), 397 - 397, English

  • 癌性間質 新しい生物指標探索の場 組織マイクロアッセイ分析(Cancerous stroma: a place to look for new biomarkers: Tissue microarray analysis)
    北野 晴久, 坂井 祐太, 田中 伴典, 黒田 揮志夫, 野本 一博, 金森 宣子, 堀 隆, 福岡 順也
    (NPO)日本肺癌学会, Oct. 2007, 肺癌, 47(5) (5), 661 - 661, English

  • 【呼吸器における薬剤有害反応と感染症】 薬剤性肺障害の病理 病理診断の役割
    福岡 順也, 田中 伴典, 堀 隆, 野本 一博
    金原出版(株), Oct. 2007, 臨床放射線, 52(10) (10), 1215 - 1225, Japanese

  • 肺の粘膜表皮癌の脱分化 2症例報告(Dedifferentiation in Pulmonary Mucoepidermoid carcinoma: Report of 2 Cases)
    田中 伴典, 坂井 祐太, 木屋 千恵子, 江尻 哲, 中川 加奈子, 福岡 順也
    (一社)日本病理学会, Apr. 2006, 日本病理学会会誌, 95(1) (1), 381 - 381, English

  • 中川 加奈子, 木屋 千恵子, 森谷 鈴子, 室坂 千鶴子, 中村 隆文, 坂井 祐太, 田中 伴典, 江尻 哲, 尾矢 剛志, 福岡 順也
    (公社)日本臨床細胞学会, Mar. 2006, 日本臨床細胞学会雑誌, 45(Suppl.1) (Suppl.1), 283 - 283, English

  • 左心室遊離壁の動脈枝の定量解析(Quantitative analysis of arterial branches of the left ventricular free wall)
    植村 健司, 田中 伴典, 大谷 裕子, 村上 弦, 大谷 修
    (一社)日本解剖学会, Mar. 2005, 解剖学雑誌, 80(Suppl.) (Suppl.), 168 - 168, English

  • 内腸骨静脈の走行異常を伴った重複下大静脈
    田中 伴典, 斉藤 勇祐, 木場 隼人, 竹村 京子, 小柳 哲男, 大谷 裕子, 大谷 修
    (一社)日本解剖学会, Mar. 2005, 解剖学雑誌, 80(Suppl.) (Suppl.), 168 - 168, Japanese

  • 橈骨神経と尺骨神経の交通枝の3例
    田中 伴典, 宮崎 晋一, 松島 千紘, 大谷 裕子, 大谷 修
    (一社)日本解剖学会, Mar. 2005, 解剖学雑誌, 80(Suppl.) (Suppl.), 256 - 256, Japanese

  • 肝臓内の動脈の走行とCouinaudの肝区域との関係
    片山 宏祐, 田中 伴典, 松尾 光浩, 大谷 裕子, 長田 拓哉, 大谷 修
    (一社)日本解剖学会, Mar. 2005, 解剖学雑誌, 80(Suppl.) (Suppl.), 258 - 258, Japanese

  • 95歳女性に見られた二分肋骨の1例
    松本 健司, 三浦 正史, 松本 裕幹, 水本 健, 田中 伴典, 松尾 光浩, 大谷 裕子, 大谷 修
    (一社)日本解剖学会, Mar. 2005, 解剖学雑誌, 80(Suppl.) (Suppl.), 259 - 259, Japanese

■ Books And Other Publications
  • Lung and Pleural Pathology
    TANAKA TOMONORI
    Joint work, Interstitial pneumonia, McGraw-Hill Education, Oct. 2015

  • マーティン神経解剖学―テキストとアトラス
    田中 伴典
    Joint translation, 西村書店, Mar. 2007

■ Lectures, oral presentations, etc.
  • The importance of lung biopsy on interstitial lung disease associated with connective disease.
    Tomonori Tanaka
    日本リウマチ学会, Apr. 2025, Japanese
    [Invited]
    Invited oral presentation

  • 間質性肺炎 基本的な見かた
    田中伴典
    日本病理学会総会, Apr. 2025, Japanese
    [Invited]
    Invited oral presentation

  • 喫煙関連肺疾患 病理の観点から
    田中伴典
    第22回若手のためのびまん性肺疾患研究会, Dec. 2024, Japanese
    [Invited]
    Keynote oral presentation

  • クライオ肺生検での病理診断の役割
    田中伴典
    第86回 浜松びまん性肺疾患研究会, Nov. 2024, Japanese
    [Invited]
    Invited oral presentation

  • クライオ肺生検の見かた・考え方 病理から見た肺癌背景肺
    田中伴典
    第32回香川びまん性肺疾患研究会, Oct. 2024, Japanese
    [Invited]
    Invited oral presentation

  • 肺癌切除検体に見られる様々な病変・肺癌背景肺の報告事項
    田中伴典
    第113回日本病理学会総会, Mar. 2024, Japanese
    [Invited]
    Nominated symposium

  • 2013年特発性間質性肺炎 ステートメントを斬る - 病理診断に関する残された課題 -
    田中伴典
    第42回日本画像医学会, Feb. 2024
    [Invited]
    Invited oral presentation

  • IgG4関連肺疾患 病理学の観点から
    田中伴典
    第20回若手のためのびまん性肺疾患勉強会, Dec. 2023
    [Invited]

  • 病理学の眼で見るびまん性肺疾患
    田中伴典
    第11回Clinical Forum of Interstitial Lung Disease, Oct. 2023
    [Invited]
    Invited oral presentation

  • 病理から見た Interstitial lung abnormalities
    田中伴典
    第83回浜松びまん性肺疾患研究会, Mar. 2023, Japanese
    [Invited]
    Invited oral presentation

  • 病理像から見た関節リウマチの多様性
    田中伴典
    第40回埼玉膠原病肺研究会, Mar. 2023, Japanese
    [Invited]
    Invited oral presentation

  • 間質性肺炎合併肺がん術後急性増悪を病理から考える
    田中伴典
    第42回画像医学会, Feb. 2023, Japanese
    [Invited]
    Invited oral presentation

  • RAの肺病理総論 -慢性線維化性ILDを中心に-
    田中伴典
    第16回びまん性肺疾患フォーラム, Dec. 2022, Japanese
    [Invited]
    Invited oral presentation

  • 間質性肺炎急性増悪 up to date
    田中伴典
    第23回東京びまん性肺疾患研究会, Oct. 2022, Japanese
    [Invited]
    Invited oral presentation

  • 病理から見たInterstitial lung abnormalities
    田中伴典
    第42回岡山胸部画像病理カンファレンス, Sep. 2022, Japanese
    [Invited]
    Invited oral presentation

  • Discussion of autopsy interstitial pneumonia on clinicopathological conference.
    Tomonori Tanaka
    第111回日本病理学会総会, Apr. 2022
    [Invited]
    Invited oral presentation

  • Defference between ARDS/DAD and COVID-19. View point of pathology.
    Tomonori Tanaka
    第15回びまん性肺疾患フォーラム, Dec. 2021
    [Invited]
    Invited oral presentation

  • Pathology of Early phase of idiopathic pulmonary fibrosis.
    Tomonori Tanaka
    第80回浜松びまん性肺疾患研究会, Oct. 2021
    [Invited]
    Invited oral presentation

  • Variety of IPF and borderline area between IPF and other disease.
    Tomonori Tanaka
    第32回びまん性肺疾患勉強会, May 2021, Japanese
    [Invited]
    Invited oral presentation

  • Diagnosis of IPF based of guideline.
    Tomonori Tanaka
    第110回日本病理学会総会, Apr. 2021, Japanese
    [Invited]
    Nominated symposium

  • 組織像からMPO-ANCA陽性の間質性肺炎を考える
    田中伴典
    第14回若手のためのびまん性肺疾患勉強会, Dec. 2020, Japanese
    [Invited]
    Invited oral presentation

  • 強皮症に伴う肺病変の病理
    田中伴典
    第39回画像医学会, Feb. 2020, Japanese
    [Invited]
    Nominated symposium

  • 間質性肺炎合併肺癌の病理
    田中 伴典
    第11回若手のためのびまん肺勉強会, Jul. 2018, Japanese, Domestic conference
    [Invited]
    Invited oral presentation

  • PPFEの概観 UIPとの関連において 病理
    田中 伴典
    第97回間質性肺疾患研究会, Jun. 2018, Japanese, Domestic conference
    [Invited]
    Keynote oral presentation

  • 皮膚筋炎合併間質性肺炎の病理
    田中 伴典
    第37回日本画像医学会, Feb. 2018, Japanese, Domestic conference
    [Invited]
    Nominated symposium

  • 間質性肺炎の病理 初歩編
    田中 伴典
    第3回初歩から学ぶびまん性肺疾患セミナー, Jan. 2018, Japanese, Domestic conference
    [Invited]
    Public discourse

  • IPF急性増悪の病理
    田中 伴典
    第11回びまん性肺疾患フォーラム, Dec. 2017, Japanese, Domestic conference
    [Invited]
    Invited oral presentation

  • Update on rare idiopathic interstitial pneumonias.
    TANAKA TOMONORI
    Pulmonary Pathology Society Biennial Meeting 2017, Jun. 2017, English, Pulmonary Pathology Society, USA, Chicago, International conference
    [Invited]
    Invited oral presentation

  • Diagnostic approach to interstitial pneumonia based on 2013 ATS/ERS classification.
    TANAKA TOMONORI
    Asia Pacific International Academy of Pathology 2017, Apr. 2017, English, International conference
    [Invited]
    Invited oral presentation

  • 急性・亜急性経過の間質性肺炎の病理像
    田中 伴典
    第36回日本画像医学会, Feb. 2017, Japanese, Domestic conference
    [Invited]
    Invited oral presentation

  • Rare idiopathic interstinal pneumonias and histologic patterns in new ATS/ERS classification
    TANAKA TOMONORI
    XXXI International Congress of the IAP and 28th Congress of the ESP, Sep. 2016, English, International conference
    [Invited]
    Invited oral presentation

  • 関節リウマチ関連肺疾患の病理像
    田中 伴典
    第6回若手のためのびまん肺勉強会, Jun. 2016, Japanese, Domestic conference
    [Invited]
    Invited oral presentation

  • 抗ARS抗体症候群の病理
    田中 伴典
    第105回日本病理学会総会JPPSコンパニオンミーティング, May 2016, Japanese, Domestic conference
    [Invited]
    Invited oral presentation

  • Subacute interstitial pneumonia ないしfibrosing OP の病理診断
    田中 伴典
    第9回びまん性肺疾患フォーラム, Dec. 2015, Japanese, Domestic conference
    [Invited]
    Invited oral presentation

  • 間質性肺炎の病理『ATS-ERS IIPs Classification』
    田中 伴典
    JCRミッドサマーセミナー, Jul. 2014, Japanese, Domestic conference
    [Invited]
    Invited oral presentation

  • サルコイドーシス/肉芽腫性肺疾患の病理
    田中 伴典
    第32回日本サルコイドーシス／肉芽腫性疾患学会総会, Oct. 2012, Japanese, Domestic conference
    [Invited]
    Invited oral presentation

■ Affiliated Academic Society
  • THE JAPANESE RESPIRATORY SOCIETY

  • THE JAPANESE SOCIETY OF PATHOLOGY

TOP