Clear Cell Papillary Renal Cell Carcinoma Incidentally Discovered in a Patient With Normal Renal Function: A Case Report

ABSTRACT Introduction Clear cell papillary renal cell carcinoma is a distinct histopathological entity first characterized in patients with end‐stage renal disease. Although increasingly reported in patients with normal renal function, it remains relatively unfamiliar in routine clinical practice. C...

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Main Authors: Toru Inoue, Masahiro Fuse, Satoki Abe, Shinya Sejiyama, Kazuhiro Kawamura, Yuzo Oyama, Tadasuke Ando, Toshitaka Shin
Format: Article
Language:English
Published: Wiley 2025-07-01
Series:IJU Case Reports
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Online Access:https://doi.org/10.1002/iju5.70050
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author Toru Inoue
Masahiro Fuse
Satoki Abe
Shinya Sejiyama
Kazuhiro Kawamura
Yuzo Oyama
Tadasuke Ando
Toshitaka Shin
author_facet Toru Inoue
Masahiro Fuse
Satoki Abe
Shinya Sejiyama
Kazuhiro Kawamura
Yuzo Oyama
Tadasuke Ando
Toshitaka Shin
author_sort Toru Inoue
collection DOAJ
description ABSTRACT Introduction Clear cell papillary renal cell carcinoma is a distinct histopathological entity first characterized in patients with end‐stage renal disease. Although increasingly reported in patients with normal renal function, it remains relatively unfamiliar in routine clinical practice. Case Presentation A 75‐year‐old male with normal renal function presented with an incidentally discovered left renal mass. Radiological evaluation revealed a mass with a distinct enhancement pattern. Considering the patient's preference for surgical management, robot‐assisted partial nephrectomy was performed, confirming clear cell papillary renal cell carcinoma, with immunohistochemistry demonstrating diffuse cytokeratin 7‐positivity, alpha‐methylacyl‐CoA racemase‐negativity, and cup‐shaped carbonic anhydrase IX staining. Conclusion This case demonstrated the characteristic features of clear cell papillary renal cell carcinoma in a patient with normal renal function. Nephron‐sparing surgery and rigorous follow‐up protocols are crucial management strategies. Future studies with larger cohorts are needed to define the natural history and optimal management of clear cell papillary renal cell carcinoma.
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issn 2577-171X
language English
publishDate 2025-07-01
publisher Wiley
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series IJU Case Reports
spelling doaj-art-c58516be7b174eba94cead0214fe8cfc2025-08-20T03:31:23ZengWileyIJU Case Reports2577-171X2025-07-018439439710.1002/iju5.70050Clear Cell Papillary Renal Cell Carcinoma Incidentally Discovered in a Patient With Normal Renal Function: A Case ReportToru Inoue0Masahiro Fuse1Satoki Abe2Shinya Sejiyama3Kazuhiro Kawamura4Yuzo Oyama5Tadasuke Ando6Toshitaka Shin7Department of Urology Faculty of Medicine, Oita University Yufu Oita JapanDepartment of Urology Faculty of Medicine, Oita University Yufu Oita JapanDepartment of Urology Faculty of Medicine, Oita University Yufu Oita JapanDepartment of Urology Faculty of Medicine, Oita University Yufu Oita JapanDepartment of Diagnostic Pathology Faculty of Medicine, Oita University Yufu Oita JapanDepartment of Diagnostic Pathology Faculty of Medicine, Oita University Yufu Oita JapanOrgan Transplantation Promotion Project Faculty of Medicine, Oita University Yufu Oita JapanDepartment of Urology Faculty of Medicine, Oita University Yufu Oita JapanABSTRACT Introduction Clear cell papillary renal cell carcinoma is a distinct histopathological entity first characterized in patients with end‐stage renal disease. Although increasingly reported in patients with normal renal function, it remains relatively unfamiliar in routine clinical practice. Case Presentation A 75‐year‐old male with normal renal function presented with an incidentally discovered left renal mass. Radiological evaluation revealed a mass with a distinct enhancement pattern. Considering the patient's preference for surgical management, robot‐assisted partial nephrectomy was performed, confirming clear cell papillary renal cell carcinoma, with immunohistochemistry demonstrating diffuse cytokeratin 7‐positivity, alpha‐methylacyl‐CoA racemase‐negativity, and cup‐shaped carbonic anhydrase IX staining. Conclusion This case demonstrated the characteristic features of clear cell papillary renal cell carcinoma in a patient with normal renal function. Nephron‐sparing surgery and rigorous follow‐up protocols are crucial management strategies. Future studies with larger cohorts are needed to define the natural history and optimal management of clear cell papillary renal cell carcinoma.https://doi.org/10.1002/iju5.70050clear cell papillary renal cell carcinomaimmunohistochemistrynormal renal function
spellingShingle Toru Inoue
Masahiro Fuse
Satoki Abe
Shinya Sejiyama
Kazuhiro Kawamura
Yuzo Oyama
Tadasuke Ando
Toshitaka Shin
Clear Cell Papillary Renal Cell Carcinoma Incidentally Discovered in a Patient With Normal Renal Function: A Case Report
IJU Case Reports
clear cell papillary renal cell carcinoma
immunohistochemistry
normal renal function
title Clear Cell Papillary Renal Cell Carcinoma Incidentally Discovered in a Patient With Normal Renal Function: A Case Report
title_full Clear Cell Papillary Renal Cell Carcinoma Incidentally Discovered in a Patient With Normal Renal Function: A Case Report
title_fullStr Clear Cell Papillary Renal Cell Carcinoma Incidentally Discovered in a Patient With Normal Renal Function: A Case Report
title_full_unstemmed Clear Cell Papillary Renal Cell Carcinoma Incidentally Discovered in a Patient With Normal Renal Function: A Case Report
title_short Clear Cell Papillary Renal Cell Carcinoma Incidentally Discovered in a Patient With Normal Renal Function: A Case Report
title_sort clear cell papillary renal cell carcinoma incidentally discovered in a patient with normal renal function a case report
topic clear cell papillary renal cell carcinoma
immunohistochemistry
normal renal function
url https://doi.org/10.1002/iju5.70050
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