Juvenile Granulosa Cell Tumor of Adult Testis: A Case Report

Ke Hsun Lin; Sey-En Lin; Liang Ming Lee

doi:10.1016/j.urology.2007.11.126

Juvenile Granulosa Cell Tumor of Adult Testis: A Case Report

Ke Hsun Lin, Sey-En Lin, Liang Ming Lee

Taipei Municipal Wanfang Hospital

Research output: Contribution to journal › Article › peer-review

13 Citations (Scopus)

Abstract

Juvenile granulosa cell tumor (JGCT) of the testis is a rare tumor and typically occurs in the testis of children aged 4 years or younger. This report describes a case of a 27-year-old man who presented with a JGCT in his right testis. Orchiectomy was performed. No recurrence was noted during an 8-year follow-up. This is the first reported case of JGCT occurring in adult testis. The benign behavior of testicular JGCT mandates that it should be distinguished from other, much more aggressive neoplasms it resembles.

Original language	English
Journal	Urology
Volume	72
Issue number	1
DOIs	https://doi.org/10.1016/j.urology.2007.11.126
Publication status	Published - Jul 2008

ASJC Scopus subject areas

Urology

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abstract = "Juvenile granulosa cell tumor (JGCT) of the testis is a rare tumor and typically occurs in the testis of children aged 4 years or younger. This report describes a case of a 27-year-old man who presented with a JGCT in his right testis. Orchiectomy was performed. No recurrence was noted during an 8-year follow-up. This is the first reported case of JGCT occurring in adult testis. The benign behavior of testicular JGCT mandates that it should be distinguished from other, much more aggressive neoplasms it resembles.",

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AB - Juvenile granulosa cell tumor (JGCT) of the testis is a rare tumor and typically occurs in the testis of children aged 4 years or younger. This report describes a case of a 27-year-old man who presented with a JGCT in his right testis. Orchiectomy was performed. No recurrence was noted during an 8-year follow-up. This is the first reported case of JGCT occurring in adult testis. The benign behavior of testicular JGCT mandates that it should be distinguished from other, much more aggressive neoplasms it resembles.

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