Primary Pure Yolk Sac Tumor of the Urinary Bladder: A Case Report

ABSTRACT Introduction Yolk sac tumors are malignant germ cell tumors that typically arise in the gonads. Although extragonadal cases have been reported, primary involvement of the urinary tract is extremely rare. Case Presentation A 67‐year‐old man presented with gross hematuria. Cystoscopy and contrast‐enhanced computed tomography revealed a 6‐cm bladder mass. Transurethral resection of the bladder tumor was performed. Histopathological and immunohistochemical findings (alpha‐fetoprotein, glypican‐3, and Sal‐like protein 4 positivity) were consistent with a yolk sac tumor without a urothelial carcinoma component. Additional examinations revealed no primary lesions elsewhere, leading to the diagnosis of a primary bladder yolk sac tumor. The patient received four cycles of etoposide and cisplatin chemotherapy and has remained recurrence‐free for 2 years. Conclusions Patients with primary bladder yolk sac tumors, although rare, may achieve favorable outcomes with combined surgical resection and chemotherapy.

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Publication Details

Journal
IJU Case Reports
Published
2026-10-15
DOI
https://doi.org/10.1002/iju5.70282
Primary Topic
Urinary and Genital Oncology Studies
Type
article
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article

Primary Pure Yolk Sac Tumor of the Urinary Bladder: A Case Report

Fumihiko Kono, Kosuke Shimizu, Masayuki Uegaki, Yuki Hashimoto et al.
IJU Case Reports
Urinary and Genital Oncology Studies
article

Primary Pure Yolk Sac Tumor of the Urinary Bladder: A Case Report

Fumihiko Kono, Kosuke Shimizu, Masayuki Uegaki, Yuki Hashimoto, Toru Yoshida
article en

Abstract

ABSTRACT Introduction Yolk sac tumors are malignant germ cell tumors that typically arise in the gonads. Although extragonadal cases have been reported, primary involvement of the urinary tract is extremely rare. Case Presentation A 67‐year‐old man presented with gross hematuria. Cystoscopy and contrast‐enhanced computed tomography revealed a 6‐cm bladder mass. Transurethral resection of the bladder tumor was performed. Histopathological and immunohistochemical findings (alpha‐fetoprotein, glypican‐3, and Sal‐like protein 4 positivity) were consistent with a yolk sac tumor without a urothelial carcinoma component. Additional examinations revealed no primary lesions elsewhere, leading to the diagnosis of a primary bladder yolk sac tumor. The patient received four cycles of etoposide and cisplatin chemotherapy and has remained recurrence‐free for 2 years. Conclusions Patients with primary bladder yolk sac tumors, although rare, may achieve favorable outcomes with combined surgical resection and chemotherapy.

IJU Case ReportsVol. 9(6)
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Urinary and Genital Oncology Studies
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