Primary neuroendocrine tumor of the testis - 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.

Written by:
Alsharif S, Al-Shraim M, Alhadi A, Al-Aown A, Fooshang F, Eid R.   Are you the author?
Department of Pathology, Armed Forces Hospital - Southern Region, Khamis Mushayt, Saudi Arabia; Department of Pathology, College of Medicine, King Khalid University, Saudi Arabia; Department of Urology, Armed Forces Hospital - Southern Region, Khamis Mushayt, Saudi Arabia.

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


PubMed Abstract
PMID: 24833836

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