睾丸原发性神经内分泌肿瘤

Primary neuroendocrine tumor of the testis.

作者信息

Alsharif Shakir, Al-Shraim Mubarak, Alhadi Ahmed, Al-Aown Abdulrahman, Fooshang Fawzy, Eid Refat

机构信息

Department of Pathology, Armed Forces Hospital - Southern Region, Khamis Mushayt, Saudi Arabia.

Department of Pathology, College of Medicine, King Khalid University, Saudi Arabia.

出版信息

Urol Ann. 2014 Apr;6(2):173-5. doi: 10.4103/0974-7796.130662.

DOI:10.4103/0974-7796.130662

PMID:24833836

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4021664/

Abstract

Testicular neuroendocrine tumor is rare. It accounts for less than 1% of all testicular neoplasms. More than 60 cases have been published in the literature. A 27-year-old man presented with left testicular mass and underwent radical orchidectomy. Histological examination showed neuroendocrine tumor, confirmed by immunohistochemistry and electron microscopy. The patient showed no evidence of metastasis over 1-year follow-up post-orchidectomy in spite of extensive tumor necrosis.

摘要

睾丸神经内分泌肿瘤较为罕见。它占所有睾丸肿瘤的比例不到1%。文献中已报道了60多例病例。一名27岁男性因左侧睾丸肿块就诊并接受了根治性睾丸切除术。组织学检查显示为神经内分泌肿瘤，经免疫组织化学和电子显微镜检查得以证实。尽管肿瘤广泛坏死，但该患者在睾丸切除术后1年的随访中未出现转移迹象。