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HYODO ToshikiUniversity Hospital / Diagnostic PathologyAssistant Professor
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■ Paper- [18F] Fluorodeoxyglucose positron emission tomography/computed tomography ([18F] FDG-PET/CT) has traditionally been considered suboptimal for the evaluation of renal tumors due to intense physiological tracer accumulation in the urinary tract. However, incidental detection of renal masses can occur during [18F] FDG-PET examinations, and recognizing that FDG uptake varies according to tumor type can aid differential diagnosis. In patients with renal failure or those undergoing dialysis, reduced urinary excretion lowers background activity, paradoxically improving the visualization of renal tumors. Recent studies have demonstrated that high-grade and sarcomatoid renal cell carcinomas (RCCs) exhibit intense [18F] FDG uptake associated with poor prognosis, whereas benign and low-grade lesions show relatively low uptake. Although [18F] FDG-PET/CT has limited sensitivity for nodal staging, it provides high diagnostic accuracy for distant metastases, including osteolytic bone lesions. During postoperative surveillance and restaging, PET/CT contributes to early detection of recurrence and assists in therapeutic decision-making, particularly in high-risk or dialysis patients. In therapeutic monitoring, changes in metabolic parameters-such as SUVmax, metabolic tumor volume, and total lesion glycolysis-correlate with progression-free and overall survival during tyrosine kinase inhibitor or immune checkpoint inhibitor therapy. These parameters complement Response Evaluation Criteria in Solid Tumors (RECIST) and support metabolic response criteria such as PET Response Criteria in Solid Tumors (PERCIST). Moreover, novel tracers developed to overcome the intrinsic limitations of [18F] FDG, including [11C] Acetate, [18F] Fluoromisonidazole, and prostate-specific membrane antigen ligands, have shown promise in differentiating fat-poor angiomyolipoma, evaluating tumor hypoxia, and detecting FDG-negative metastases. This review discusses the current role, limitations, and future perspectives of [18F] FDG-PET in the management of renal tumors, with particular focus on RCC.Nov. 2025, Seminars in nuclear medicine, English, International magazineScientific journal
- PURPOSE: Fumarate hydratase (FH)-deficient renal cell carcinoma (RCC) is a rare and aggressive RCC subtype defined in the 2022 WHO classification. This study aimed to describe its imaging and clinicopathological features. METHODS: A retrospective analysis was conducted on 11 patients (12 tumors) diagnosed with FH-deficient RCC between 2015 and 2024 across multiple institutions. Clinical data, imaging findings (CT, MRI, [18F] fluorodeoxyglucose (FDG) -PET/CT), and histopathological results were reviewed. RESULTS: The median age at diagnosis was 54 years (range: 35-81), with a male predominance (64%). At presentation, distant metastases were observed in 27% of patients. Based on contrast-enhanced CT findings, tumors were morphologically classified into three types: cystic-predominant (n = 5), solid-predominant (n = 4), and purely solid (n = 3). The dynamic enhancement pattern of the solid components showed progressive enhancement in 54.5% and mild corticomedullary enhancement with delayed washout in 45.5%, suggesting vascular heterogeneity. MRI showed high signal intensity of cystic components on both T1WI and T2WI, suggestive of hemorrhage. Solid components exhibited restricted diffusion on DWI in all cases, with a median ADC value of 0.88 (range: 0.77-1.18) × 10⁻³ mm²/s. On FDG-PET/CT, solid components demonstrated elevated FDG uptake (median SUVmax: 7.25; range: 6.81-10.10). Among nine cases with available follow-up data, three (33%) developed recurrence within two years after surgery. CONCLUSION: FH-deficient RCC has a high risk of metastasis and recurrence, requiring strict follow-up. Although definitive diagnosis relies on immunohistochemistry, imaging features-such as mixed cystic-solid morphology, hemorrhagic cysts, and, compared with clear cell RCC, lower enhancement, restricted diffusion, and higher FDG uptake-may serve as important diagnostic clues that facilitate accurate pathological diagnosis and management.Nov. 2025, Abdominal radiology (New York), English, International magazineScientific journal
- The objective of this article is to provide a comprehensive overview of the imaging characteristics of various renal cell tumors using 18F-fluorodeoxyglucose (FDG)-positron emission tomography (PET), based on the latest WHO-2022 classification. Due to the physiological accumulation of FDG in the kidneys, the clinical utility of FDG-PET in the evaluation of renal tumors has traditionally been considered limited. However, recent studies have re-evaluated its potential value. FDG-PET has demonstrated particular utility in detecting metastases and postoperative recurrence of renal cell carcinoma (RCC), as well as in identifying RCC in patients with chronic kidney failure, where FDG excretion into the urinary tract is reduced. Renal tumors are occasionally detected incidentally on FDG-PET, and FDG uptake varies depending on the tumor subtype. Therefore, a comprehensive understanding of these imaging characteristics is clinically important, as it may serve as a valuable guide for subsequent diagnostic evaluations. Furthermore, recent advancements in the development of novel PET tracers hold promise for future applications in the imaging of renal tumors. We believe that the insights gained from this study will contribute to routine diagnostic practice and the planning of future research.Jul. 2025, Japanese journal of radiology, 43(7) (7), 1078 - 1089, English, Domestic magazineScientific journal
- Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a complication caused by antithyroid drugs, particularly propylthiouracil (PTU). Most patients experience organ failure due to the affects of the treatment regimen. We herein report the case of an 89-year-old woman whose severe AAV induced by PTU resulted in various instances of organ failure that eventually led to death after 9 years of PTU therapy. During autopsy, we identified five types of organ failure. As AAV is a potentially fatal disease, the development of various vasculitis symptoms during PTU therapy should therefore be carefully monitored.Dec. 2024, Internal medicine (Tokyo, Japan), 63(23) (23), 3197 - 3202, English, Domestic magazineScientific journal
- PURPOSE: To compare the image quality, inter-reader agreement, and diagnostic capability for muscle-invasive bladder cancer (MIBC) of the reconstructed images in sections orthogonal to the bladder tumor obtained by 3D Dynamic contrast-enhanced (DCE)-MRI using the Golden-angle Radial Sparse Parallel (GRASP) technique with the images directly captured using the Cartesian sampling. MATERIALS AND METHODS: This study involved 68 initial cases of bladder cancer examined with DCE-MRI (GRASP: n = 34, Cartesian: n = 34) at 3 Tesla. Four radiologists conducted qualitative evaluations (overall image quality, absence of motion artifact, absence of streak artifact, and tumor conspicuity) using a five-point Likert scale (5 = Excellent/None) and quantitative signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR) measurements. The areas under the receiver-operating characteristic curves (AUCs) for the Vesical Imaging-Reporting and Data System (VI-RADS) DCE score for MIBC assessment were calculated. Inter-reader agreement was also assessed. RESULTS: GRASP notably enhanced overall image quality (pooled score: GRASP 4 vs. Cartesian 3, P < 0.0001), tumor conspicuity (5 vs. 3, P < 0.05), SNR (Median 38.2 vs. 19.0, P < 0.0001), and CNR (7.9 vs. 6.0, P = 0.005), with fewer motion artifacts (5 vs. 3, P < 0.0001) and minor streak artifacts (5 vs. 5, P > 0.05). Although no significant differences were observed, the GRASP group tended to have higher AUCs for MIBC (pooled AUCs: 0.92 vs. 0.88) and showed a trend toward higher inter-reader agreement (pooled kappa-value: 0.70 vs. 0.63) compared to the Cartesian group. CONCLUSIONS: Using the GRASP for 3D DCE-MRI, the reconstructed images in sections orthogonal to the bladder tumor achieved higher image quality and improve the clinical work flow, compared to the images directly captured using the Cartesian. GRASP tended to have higher diagnostic ability for MIBC and showed a trend toward higher inter-reader agreement compared to the Cartesian.Dec. 2024, Japanese journal of radiology, 42(12) (12), 1469 - 1478, English, Domestic magazineScientific journal
- Neural epidermal growth factor-like 1 protein (NELL1) is the second most common target antigen in membranous glomerulonephritis (MGN). However, data regarding the clinicopathological characteristics of NELL1-associated MGN are limited owing to its low prevalence. This study examined the prevalence and clinicopathological characteristics of NELL1-associated MGN in a Japanese cohort. Additionally, we compared the clinicopathological features of NELL1-positive MGN, phospholipase A2 receptor 1 (PLA2R1)-positive MGN, and MGN negative for all three antigens (NELL1, PLA2R1, and thrombospondin type-1 domain-containing 7A). Among 257 consecutive patients pathologically diagnosed with MGN at two centers in Japan, 24 (9.3%) were immunohistochemically positive for NELL1. Clinically, patients with NELL1-positive MGN were significantly older (p < 0.001) and had a higher frequency of bucillamine use (vs PLA2R1-positive MGN, p < 0.01). Histologically, NELL1-positive MGN exhibited significantly lower detection of spikes and crater formation (p < 0.001), higher prevalence of segmental spike distribution (vs PLA2R1-positive MGN: p < 0.001), and higher prevalence of stage I cases on electron microscopy (p < 0.01). There were no significant differences in the prognoses among the three groups. The characteristic histological feature of segmental distribution in NELL1-positive MGN may be related to bucillamine use and the early phase of the disease. Further investigations with larger numbers of patients may offer further insight into the prognosis of patients with NELL1-positive MGN.Sep. 2024, Virchows Archiv : an international journal of pathology, 486(5) (5), 991 - 1000, English, International magazineScientific journal
- PURPOSE: Tubulointerstitial nephritis (TIN) has various etiologies, including IgG4-related disease (IgG4-RD), autoimmune diseases, antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), and others. IgG4-positive plasma cell infiltration can occasionally be found in TIN unrelated to IgG4-RD. Therefore, there may be problems with usage of IgG4 immunostaining to differentiate between TIN with and TIN without IgG4-RD. This study aimed to compare the proportion of plasma cells that are positive for each IgG subclass and to clarify the predominant IgG subclass trends and clinical characteristics associated with IgG4-RD and non-IgG4-related interstitial nephritis. METHODS: The study enrolled 44 cases of TIN: 6 of IgG4-RD, 8 of autoimmune disease, 9 of AAV, and 21 of unknown disease group. In addition to clinical characteristics, IgG subclass composition of interstitial plasma cells was evaluated among 4 groups by immunohistochemistry. RESULTS: IgG1 was the predominant IgG subclass in TIN unrelated to IgG4-RD. In the IgG4-RD group, the IgG subclass rate was high in both IgG1 and IgG4. The rate of average IgG4-positive cells was significantly lower in the autoimmune disease group and unknown disease group compared with the IgG4-RD group. CONCLUSION: The present study revealed IgG1-dominant immune profiles of TIN unrelated to IgG4-RD. Further investigation is required to elucidate the clinicopathological differences between IgG1-dominant and IgG4-dominant groups in IgG4-RD.Feb. 2024, International urology and nephrology, 56(7) (7), 2363 - 2369, English, International magazineScientific journal
- Not all patients with ulcerative colitis (UC) respond initially to treatment with biologic agents, and predicting their efficacy prior to treatment is difficult. Vedolizumab, a humanized monoclonal antibody against alpha 4 beta 7 (α4β7) integrin, suppresses immune cell migration by blocking the interaction between α4β7 integrin and mucosal addressin cell adhesion molecule 1. Reports about histological features that predict vedolizumab efficacy are scarce. So, we examined the association between histological features and vedolizumab efficacy. This was a multicenter, retrospective study of patients with UC treated with vedolizumab. Biopsy specimens taken from the colonic mucosa prior to vedolizumab induction were used, and the areas positively stained for CD4, CD68, and CD45 were calculated. Clinical and histological features were compared between those with and without remission at week 22, and the factors associated with clinical outcomes were identified. We enrolled 42 patients. Patients with a high CD4+ infiltration showed a better response to vedolizumab [odds ratio (OR) = 1.44, P = 0.014]. The concomitant use of corticosteroids and high Mayo scores had a negative association with the vedolizumab response (OR = 0.11, P = 0.008 and OR = 0.50, P = 0.009, respectively). Histological evaluation for CD4+ cell infiltration may be helpful in selecting patients who can benefit from vedolizumab.Nov. 2023, Scientific reports, 13(1) (1), 20262 - 20262, English, International magazineScientific journal
- KEY CLINICAL MESSAGE: Renal cell carcinoma as a secondary malignant neoplasm is relatively rare; however, the possibility of secondary renal cell carcinoma following chemoradiotherapy for childhood nephroblastoma should be considered. ABSTRACT: The occurrence of secondary renal cell carcinoma (RCC) following chemoradiotherapy for nephroblastoma is relatively rare, especially in microphthalmia transcription factor family translocation renal cell carcinoma. A 13-year-old Japanese male was referred to our department for treatment of a right kidney mass. The patient had undergone open left nephrectomy and adjuvant chemotherapy for nephroblastoma, 12 years before. Diagnostic imaging revealed a tumor in the right kidney and a lesion suspected to be metastasis in the left eighth rib. Chromophobe RCC or translocation RCC was suspected from the imaging pattern. TNM classification was cT1aN0M1, and the clinical stage was IV. Partial nephrectomy by robot-assisted surgery for the right renal tumor and resection of the left eighth rib were performed. Pathologically, the renal tumor was diagnosed as translocation RCC, and the rib lesion demonstrated no evidence of malignancy. We are currently undergoing imaging follow-up and the patient has been recurrence-free for 15 months. In this study, we present a rare case of secondary translocation RCC after successful treatment of nephroblastoma.Nov. 2023, Clinical case reports, 11(11) (11), e8128, English, International magazineScientific journal
- BACKGROUND Various neoplasms, including neuroendocrine neoplasms (NENs), can arise from the presacral space. Most presacral lesions are detected due to symptoms arising from tumor growth. However, diagnosing small, asymptomatic presacral tumors is challenging because of their unique location. CASE REPORT A 63-year-old woman with chronic hepatitis C underwent follow-up after achieving a sustained virological response. Abdominal ultrasonography revealed multiple new hyperechoic masses in the liver. Physical and laboratory examinations, including tumor marker analysis, yielded unremarkable results. Computed tomography (CT) and magnetic resonance imaging (MRI) indicated metastatic liver tumors but failed to identify the primary site of these lesions. The hepatic mass was biopsied, leading to a diagnosis of grade 2 neuroendocrine tumor. 111In-pentetreotide somatostatin receptor scintigraphy revealed significant radiotracer accumulation in multiple hepatic masses, several bones, and a small presacral space lesion. Pathological examination of the presacral lesion confirmed a grade 2 neuroendocrine tumor, similar to the hepatic mass. Review of a CT scan performed 4 years earlier indicated a small cyst-like lesion in the presacral space suspected of being a developmental cyst; however, the presence of cystic components was not confirmed pathologically. The patient was diagnosed with a primary presacral neuroendocrine tumor, which might have originated from a developmental cyst, with multiple liver metastases. Chemotherapy with everolimus was initiated, and the clinical course has been uneventful. CONCLUSIONS We report a rare neuroendocrine tumor arising from the presacral space with multiple liver metastases. The presacral space should be examined when a NEN with an unknown primary site is found.Jul. 2023, The American journal of case reports, 24, e939614, English, International magazineScientific journal
- A 79-year-old female was diagnosed with a right renal tumor with a level II tumor thrombus of the vena cava. presurgical therapy was initiated with a combination of avelumab and axitinib for 3 monthes. Then, she underwent nephrectomy and thrombectomy. Histologically, the primary tumor and tumor thrombus had no viable cells, indicating that pathological complete response was achieved with presurgical tyrosine kinase inhibitor/Immuno-oncology combination therapy. An immunohistological xamination showed very strong staining for tumor-infiltrating lymphocytes in the embolized area of the tumor, with CD8 predominating over CD4.Nov. 2021, Urology case reports, 39, 101800 - 101800, English, International magazine
- (株)文光堂, Jun. 2021, 病理と臨床, 39(6) (6), 611 - 616, Japanese
- A 78-year-old man who underwent right nephrectomy for renal cell carcinoma (RCC) 18 years ago visited our hospital complaining of abdominal pain. Imaging revealed that the pancreatic head tumor obstructed the Santorini duct. We suspected a pancreatic intraductal tumor, such as an intraductal tubulopapillary neoplasm or intraductal papillary mucinous neoplasm. Thus, the patient underwent subtotal stomach-preserving pancreaticoduodenectomy. Pathological findings confirmed the diagnosis of metastatic RCC. Herein, we report a case of pancreatic metastasis of an RCC that presented with a tumor in the pancreatic duct.Jun. 2021, Clinical journal of gastroenterology, 14(3) (3), 905 - 909, English, Domestic magazineScientific journal
- BACKGROUND Microscopic tumor foci have been detected incidentally on renal biopsy, including renal cell carcinoma and renomedullary interstitial cell tumor (medullary fibroma). A report is presented of a case of an incidental finding of microscopic renal angiomyolipoma that was diagnosed and completely excised on core needle biopsy. CASE REPORT A 44-year-old woman was referred to our hospital for evaluation of persistent mild proteinuria. Three years previously, she was diagnosed with Cushing's syndrome associated with a right adrenal cortical adenoma, which was successfully treated with unilateral adrenalectomy. At the time of surgery, abdominal computed tomography (CT) showed no renal lesions. During the present admission, a renal biopsy was performed that showed minimal changes in the renal glomeruli and interstitium. Immunofluorescence showed weakly positive staining for IgM in the glomeruli and no dense deposits. A microscopic focus of a predominantly spindle-cell tumor was found in the corticomedullary region. Immunohistochemistry showed positive immunostaining for HMB-45, Melan-A, and alpha-smooth muscle actin (ASMA), which supported a diagnosis of angiomyolipoma. Abdominal ultrasound at one-year follow-up showed no evidence of residual renal tumor. CONCLUSIONS To our knowledge, this is the first reported case of a completely excised incidental microscopic renal angiomyolipoma. This case demonstrated that even when imaging findings are normal, renal biopsy may detect microscopic foci of primary renal tumors.Mar. 2020, The American journal of case reports, 21, e921353, English, International magazine
- (一社)日本肝臓学会, Mar. 2020, 肝臓, 61(3) (3), 122 - 128, Japanese
- Thrombospondin type 1 domain-containing 7A (THSD7A) is a recently identified target antigen of idiopathic membranous nephropathy (iMN). The clinicopathological characteristics of THSD7A-associated MN are poorly characterised due to low prevalence among MN patients. Among 469 consecutive cases of pathologically confirmed MN diagnosed at four centres in Japan, 14 cases were confirmed positive for THSD7A by immunohistochemistry (3.0%). The prevalence of THSD7A-associated MN tended to be higher in northern Japan. Most cases demonstrated nephrotic-range proteinuria (12/14 cases, 86%). In two patients, cancer was detected at the time of renal biopsy (small-cell carcinoma of the lung and prostatic adenocarcinoma with neuroendocrine differentiation). Both tumours were negative for THSD7A. Four patients had concurrent or previous incidence of allergic diseases, including one patient with Kimura's disease. Pathological analysis of kidney biopsy tissue revealed slight mesangial cell proliferation in three cases and spike formation in one case. Immunofluorescence studies demonstrated that IgG subclass was mainly IgG4-dominant/codominant (12/13, 92% cases), while the case with prostatic cancer had an IgG2-dominant distribution. The immunostaining profile for components of the lectin complement pathways was not significant in three cases including two patients with malignancy. One case was dual positive for THSD7A and PLA2R. Of 10 cases with known clinical follow-up data, 6 demonstrated reduced serum creatinine and 8 presented reduced proteinuria. In summary, although the major IgG phenotype was usually IgG4-dominant/codominant, clinical background was otherwise heterogeneous. Further investigation of regional differences in THSD7A-associated MN prevalence may reveal genetic and environmental risk factor and associated pathogenic mechanisms.Jun. 2019, Virchows Archiv : an international journal of pathology, 474(6) (6), 735 - 743, English, International magazineScientific journal
- A 77-year-old man was referred to our hospital with persistent proteinuria and progressive lower leg edema. Past history was unremarkable except for hypertension. Autoimmune diseases, infections, and malignancies were excluded based on clinical and laboratory test results. Renal biopsy specimens showed membranous nephropathy with segmental distribution of spikes and bubbling appearance. Double contour formation in glomerular tufts was also observed. There were no proliferative changes in the glomeruli. Interstitial fibrosis and tubular atrophy were moderate, and no interstitial inflammation was observed. Arteries showed moderate sclerotic changes with hyalinosis. Immunohistochemical analysis revealed no thrombospondin type 1 domain-containing 7A reactivity. Immunofluorescence staining showed segmental granular positivity of IgG on glomerular tufts and focal staining of IgG on the tubular basement membranes. IgG deposits (subclass distribution: IgG1, 2+; IgG2, -; IgG3, 1+; IgG4, 2+) and phospholipase A2 receptor type 1 (PLA2R1) immunoreactivity showed similar distributions in both glomeruli and renal tubular basement membranes. Electron microscopy revealed subendothelial edema in partially collapsed glomerulus. No subepithelial dense deposits were observed in the glomeruli under an electron microscope. This is the first documented case of membranous nephropathy (MN) with segmental distribution of PLA2R1 in the glomeruli and focal PLA2R1 positivity in renal tubular basement membranes. Our findings extend the pathological presentation of PLA2R1-associated MN. Future studies are required to examine the mechanistic insights of these atypical histopathological features. .Feb. 2019, Clinical nephrology, 91(2) (2), 114 - 119, English, International magazineScientific journal
- Renal cell carcinoma (RCC) occasionally has sarcomatoid differentiation and rarely contains heterologous components. We report a case of chromophobe RCC with sarcomatoid differentiation that had various heterologous components including a unique lipomatous area. The patient was an 83-year-old woman with a palpable mass in the left lower abdomen. Grossly, the tumor was 14 cm in diameter and had yellowish-to-whitish color with focal necrosis and hemorrhage. Histologically, the tumor was composed of an eosinophilic subtype of chromophobe RCC with sarcomatoid differentiation including mainly chondrosarcoma, some osteosarcoma and a lipomatous area. The heterologous components of sarcomatoid RCC are usually osteosarcoma or chondrosarcoma, and sarcomatoid RCC with multiple heterologous components is extremely rare.Sep. 2018, Pathology international, 68(9) (9), 524 - 529, English, International magazineScientific journal
- 2018, CASE REPORTS IN ONCOLOGY, 11(3) (3), 735 - 741, EnglishScientific journal
- (株)東京医学社, Sep. 2024, 腎と透析, 97(3) (3), 383 - 390, Japanese
- (株)文光堂, Apr. 2023, 病理と臨床, 41(臨増) (臨増), 133 - 133, Japanese
- (株)文光堂, Apr. 2023, 病理と臨床, 41(臨増) (臨増), 134 - 134, Japanese
- 2021, 病理と臨床, 39(4) (4)マクロクイズ 第144回
- 文光堂, Apr. 2023, Japanese病理診断クイックリファレンス 2023/ 「病理と臨床」編集委員会編
- 文光堂, Nov. 2022, Japanese, ISBN: 9784830604881腎
- 移植, Oct. 2025, Japanese, (一社)日本移植学会移植後拒絶を疑う腎機能低下から腎動脈狭窄が判明した一例
- 臨床放射線, Jul. 2025, Japanese, 金原出版(株)膿瘍形成をきたした巨大嚢胞性子宮腺筋症の1例
- 日本腎臓学会誌, Jun. 2025, Japanese, (一社)日本腎臓学会腎生検病理診断コンサルテーション・アンド・レビュー (症例1)大動脈周囲の軟部影と高IgG4血症及び腎機能障害を認めた一例
- 日本腎臓学会誌, Jun. 2025, Japanese, (一社)日本腎臓学会ADTKD-MUC1診断における免疫蛍光染色の有用性
- 日本小児腎臓病学会雑誌, May 2025, Japanese, (一社)日本小児腎臓病学会ADTKD-MUC1診断における免疫蛍光染色の有用性
- 日本病理学会会誌, Mar. 2025, English, (一社)日本病理学会NELL1関連膜性腎症の臨床病理学的特徴(Clinicopathological characteristics of NELL 1-associated membranous glomerulonephritis)
- 日本病理学会会誌, Mar. 2025, English, (一社)日本病理学会急性肝不全を契機に診断に至ったランゲルハンス細胞肉腫の一例(A case of Langerhans cell sarcoma found with acute liver failure)
- 核医学, 2025, Japanese, (一社)日本核医学会腎腫瘍のFDG-PET所見-WHO分類第5版(2022)に基づいて
- 移植, Nov. 2024, Japanese, (一社)日本移植学会抗ネフリン抗体の関与が疑われた巣状分節性糸球体硬化症の腎移植後再発の一例
- 日本臨床細胞学会雑誌, Oct. 2024, Japanese, (公社)日本臨床細胞学会ホブネイル(hobnail)様異型細胞が混在した甲状腺乳頭癌の一例
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- 日本腎臓学会誌, Sep. 2024, Japanese, (一社)日本腎臓学会尿円柱・結晶に関する腎病変
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- 日本腎臓学会誌, Jun. 2024, Japanese, (一社)日本腎臓学会免疫蛍光染色によるADTKD-MUC1診断法の確立
- 日本小児腎臓病学会雑誌, May 2024, Japanese, (一社)日本小児腎臓病学会免疫蛍光染色によるADTKD-MUC1診断法の確立
- 日本病理学会会誌, Feb. 2024, English, (一社)日本病理学会甲状腺に発生し未分化癌との鑑別に難渋した悪性グロムス腫瘍の1例(Malignant glomus tumor of the thyroid gland: a difficult-to-diagnose case)
- 日本病理学会会誌, Feb. 2024, English, (一社)日本病理学会Fumarate hydratase(FH)欠損性腎細胞癌と考えられた一例(A case of renal cell carcinoma, suggesting fumarate hydratase(FH)-deficient)
- 日本腎臓学会誌, Sep. 2023, Japanese, (一社)日本腎臓学会COVID-19感染を契機にネフローゼ症候群を発症し,膜性増殖性糸球体腎炎(MGPN)と診断された1例
- 日本腎臓学会誌, Sep. 2023, Japanese, (一社)日本腎臓学会COVID-19契機に非典型的溶血性尿毒症症候群(aHUS)を発症し維持透析に至った若年者の一例
- 日本内分泌学会雑誌, Mar. 2023, Japanese, (一社)日本内分泌学会甲状腺未分化癌の術後に再発や転移なく4年間経過している症例
- 日本内分泌学会雑誌, Feb. 2023, Japanese, (一社)日本内分泌学会甲状腺未分化癌を完全切除でき、転移や術後再発なく4年間が経過している症例
- 日本腎臓学会誌, Oct. 2022, Japanese, (一社)日本腎臓学会糸球体優位にM蛋白を貪食した組織球を認めたリンパ形質細胞性リンパ腫によるcrystal-storing histiocytosisの1症例
- 日本腎臓学会誌, Oct. 2022, Japanese, (一社)日本腎臓学会クリオフィブリノゲン関連腎症の一例
- 日本形成外科学会会誌, Apr. 2022, Japanese, (一社)日本形成外科学会母指指動脈の切断、吻合による再建が必要であった母指筋周皮腫の一例
- 日本病理学会会誌, Mar. 2022, Japanese, (一社)日本病理学会Renal medullary angiitis4例の臨床病理学的検討
- 日本病理学会会誌, Mar. 2022, Japanese, (一社)日本病理学会微小変化型ネフローゼ症候にみられるIgG dustingの検討
- 日本病理学会会誌, Mar. 2022, Japanese, (一社)日本病理学会尿細管間質性腎炎55例の免疫組織化学染色を用いたIgG subclass検討
- 日本病理学会会誌, Mar. 2022, Japanese, (一社)日本病理学会軽鎖免疫グロブリン貪食組織球の顕著な管内増殖性糸球体腎炎の1例
- 日本腎臓学会誌, Sep. 2021, Japanese, (一社)日本腎臓学会難治性重症ネフローゼ症候群に対し免疫抑制療法と血漿交換により完全寛解に至ったSLEの一例
- 日本腎臓学会誌, Sep. 2021, Japanese, (一社)日本腎臓学会Medullary angiitisと診断した腎膿瘍疑い症例
- 日本内分泌学会雑誌, Apr. 2021, Japanese, (一社)日本内分泌学会Basedow病治療中にANCA関連血管炎を発症し、血管炎の病理所見を得た高齢女性の一例
- 日本内分泌学会雑誌, Oct. 2020, Japanese, (一社)日本内分泌学会PTU服用開始9年後にANCA関連血管炎を発症した一例
- 日本腎臓学会誌, Sep. 2020, Japanese, (一社)日本腎臓学会感染後糸球体腎炎を契機に発症した高齢者微小変化型ネフローゼ症候群のステロイド治療完全寛解症例
- 日本病理学会会誌, Mar. 2020, Japanese, (一社)日本病理学会Oligomeganephronia9例の臨床病理学的検討
- 日本医学放射線学会秋季臨床大会抄録集, Sep. 2019, Japanese, (公社)日本医学放射線学会腸間膜に発生した悪性末梢神経鞘腫の1例
- 日本腎臓学会誌, May 2019, Japanese, (一社)日本腎臓学会ゲフィチニブで治療中に急速進行性糸球体腎炎の経過を辿った肺がん患者の1例
- 日本内分泌学会雑誌, Apr. 2019, Japanese, (一社)日本内分泌学会痩せ型糖尿病と筋力低下から診断に至ったクッシング症候群の1例
- 日本内分泌学会雑誌, Apr. 2019, Japanese, (一社)日本内分泌学会急速に健忘、意欲低下が進行した鞍上部血管腫の1例
- 日本病理学会会誌, Apr. 2019, Japanese, (一社)日本病理学会Fabry病遺伝子変異と腎病理像 E66Q変異はFabry病か否か?
- 日本内分泌学会雑誌, Dec. 2018, Japanese, (一社)日本内分泌学会皮膚筋炎の診断から発見に至った甲状腺乳頭癌の1例
- 日本乳癌学会総会プログラム抄録集, May 2018, Japanese, (一社)日本乳癌学会乳癌の卵巣転移と原発性卵巣癌の鑑別が困難であった1症例
- 日本病理学会会誌, Apr. 2018, Japanese, (一社)日本病理学会結晶様構造物を伴う近位尿細管障害像をきたした多発性骨髄腫の一例
- 肝臓, 2018肝細胞癌治療経過中に神経内分泌癌を合併したC型肝硬変の一剖検例
■ Research Themes