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Author Spotlight: Genetically Engineered Mouse Models and Pathological Characterization of Neurofibromatosis Type 1 Associated Tumors
Published on: May 17, 2024
Primary neuroendocrine tumor of the testis
Shakir Alsharif1, Mubarak Al-Shraim2, Ahmed Alhadi3
1Department of Pathology, Armed Forces Hospital - Southern Region, Khamis Mushayt, Saudi Arabia.
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.
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