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Primary seminal vesicle adenocarcinoma: A case report of rare entity and discussion of its differential diagnosis using immunohistochemical approach for the core biopsy specimen

机译:原发性精囊腺癌:使用免疫组化方法对核心活检标本的少数实体罕见实体和鉴别诊断的案例报告

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摘要

Abstract Primary seminal vesicle adenocarcinoma is a rare malignancy of the male genito‐urinary system with only a few confirmed reported cases. Initial tissue diagnostic modality is often a core biopsy specimen. Here, we report this rare entity in a 50‐year‐old male, highlighting the histomorphological and immunohistochemical approach to the core biopsy specimen of the seminal vesicle mass. The patient presented with a history of haematospermia and gross haematuria for one year, and radiological workup was found to have a right seminal vesicle mass. A trans‐rectal ultrasound guided core biopsy revealed a tumourous lesion with a predominant papillary architecture and cytological features of neoplasia. Based on positivity for CK7, PAX‐8 and CA‐125, and Ki‐67 index of 30%–40% and negativity for PSA, AMACR, CK20, CDX‐2, p63, GATA3, WT1 and calretinin, a diagnosis of primary seminal vesicle adenocarcinoma was offered. The diagnosis was also confirmed on the surgically resected specimen. This case depicts the approach of a pathologist to diagnose this rare entity on the core biopsy specimen and the possible differential diagnoses one must consider.
机译:摘要初级精髓囊泡腺癌是雄性泌尿系统的罕见恶性肿瘤,只有少数证实报告的病例。初始组织诊断模态通常是核心活组织检查标本。在这里,我们在50岁的男性中报告了这种罕见的实体,突出了精囊囊泡质量的核心活检标本的组织形态和免疫组织化学方法。患有血红蛋白历史和血腥血尿历史一年的患者,发现放射性处理具有正确的精囊囊泡。反外直肠超声引导核心活组织检查显示肿瘤病变,其具有主要的乳头结构和瘤形成的细胞学特征。基于CK7,PAX-8和CA-125的阳性,KI-67指数为30%-40%,PSA,AMACR,CK20,CDX-2,P63,GATA3,WT1和CALRETININ的消极性,诊断提供了精囊腺癌。还在手术切除的标本上证实了诊断。这种情况描绘了病理学家的方法,以诊断核心活检标本上的这种罕见实体,并且必须考虑可能的差异诊断。

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