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CASE REPORT
Year : 2014  |  Volume : 6  |  Issue : 2  |  Page : 173-175

Primary neuroendocrine tumor of the testis


1 Department of Pathology, Armed Forces Hospital - Southern Region, Khamis Mushayt, Saudi Arabia
2 Department of Pathology, College of Medicine, King Khalid University, Saudi Arabia
3 Department of Urology, Armed Forces Hospital - Southern Region, Khamis Mushayt, Saudi Arabia

Correspondence Address:
Mubarak Al-Shraim
Department of Pathology, King Khalid University, College of Medicine, 61421 Abha, PO Box 641
Saudi Arabia
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DOI: 10.4103/0974-7796.130662

PMID: 24833836

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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.


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