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Clear Cell Primary Seminal Vesicle Carcinoma in a Young Male-A Rare Case Report

机译:年轻男性男性中的透明细胞原代精囊泡癌罕见病例报告

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Primary malignancies of Seminal Vesicle (SV) are rare. When involved, it is most commonly due to secondaries or by contiguousspread from adjacent organs. Primary tumours that can arise in SV can be epithelial and mesenchymal. Adenocarcinoma is mostcommon epithelial tumour, and the Clear Cell variant of Adenocarcinoma (CCA) so far has not been reported in literature. PrimarySV malignancies like adenocarcinoma pose a diagnostic dilemma as it becomes diffcult to differentiate it from secondaries or asinvolvement from other adjacent organs even with imaging, histopathology and Immunohistochemistry (IHC). Here we present acase of 34-year-old male who presented with occasional total painless haematuria for four years and was evaluated by ContrastEnhanced Computed Tomography (CECT) which revealed pelvic mass. After evaluation by biopsy, histopathology and IHC he wasdiagnosed as primary clear cell adenocarcinoma. Despite all investigations this malignancy is diffcult to differentiate from mullerianduct cyst carcinoma.
机译:精囊(SV)的原发恶性肿瘤很少见。当涉及时,最常见是由于次生或邻近器官的连续扩散所致。 SV中可能出现的原发性肿瘤可能是上皮和间质。腺癌是最常见的上皮肿瘤,迄今为止,腺癌(CCA)的透明细胞变异尚未在文献中报道。原发性SV恶性肿瘤(如腺癌)造成诊断难题,因为即使通过影像学,组织病理学和免疫组织化学(IHC)很难将其与继发性或累及其他邻近器官区分开。在这里,我们介绍了一例34岁的男性患者,该患者偶尔出现完全性无痛性血尿,持续了四年,并通过对比增强计算机断层扫描(CECT)进行了评估,结果显示了骨盆肿块。经活检,组织病理学和IHC评估后,他被诊断为原发性透明细胞腺癌。尽管进行了所有研究,但这种恶性肿瘤很难区别于mullerianduct囊肿癌。

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