睾丸幼年型颗粒细胞瘤：一例报告

Testicular juvenile granulosa cell tumor: a case report.

作者信息

Baldazzi Michelangelo, Rossi Eugenio, Minelli Rocco, Paviglianiti Giuseppe, Napolitano Marcello, Romeo Paolo, Galuppi Francesco, Di Vincenzo Anna Olga, Greco Laura, Vivacqua Donatella, Thomas Eduje, Lovato Luigi, Lima Mario

机构信息

Pediatric and Adult CardioThoracic and Vascular, Oncohematologic and Emergency Radiology Unit, IRCCS Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy.

U.O.S.D. Diagnostica Per Immagini A.O.R.N. Santobono-Pausilipon, Pausilipon Hospital, Naples, Italy.

出版信息

J Ultrasound. 2024 Jun 16. doi: 10.1007/s40477-024-00905-9.

DOI:10.1007/s40477-024-00905-9

PMID:38879834

Abstract

The Testicular Juvenile Granulosa Cell Tumor (JGCT) is a rare testicular neoplasm that appears in the first months of life as a painless testicular mass. Following an accurate radiological ultrasound diagnosis, through which the cystic appearance of the lesion is observed, and histological confirmation, showing follicular growth pattern and an immunoreactivity for inhibin, the treatment process involves, when feasible, conservative surgery. We present the case of a 2-months old infant with a bilateral JGCT of the testis and we review the classical findings of the patology.

摘要

睾丸幼年型颗粒细胞瘤（JGCT）是一种罕见的睾丸肿瘤，在出生后的头几个月表现为无痛性睾丸肿块。在通过精确的放射超声诊断观察到病变的囊性外观并经组织学确认显示滤泡生长模式和抑制素免疫反应性后，治疗过程在可行时包括保守手术。我们报告一例2个月大双侧睾丸JGCT婴儿的病例，并回顾该病理学的经典发现。