VON Hippel-Lindau综合征:附睾囊腺瘤合并血精症的罕见病例

IF 0.4 Q4 UROLOGY & NEPHROLOGY
Paulo Victor de Jesus Silva, Leonardo Bernardes de Amaro, Guilherme Vieira Cavalcante, Jefferson Douglas Camargos Moreira, Wagner Eduardo Matheus
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引用次数: 0

摘要

Von Hippel-Lindau (VHL)病可引起附睾囊腺瘤,通常无症状。我们报告一位27岁男性VHL病史(切除中枢神经系统血管母细胞瘤),表现出异常的复发性血精和双侧附睾肿大。超声和CT证实双侧附睾病变和其他vhl相关发现(胰腺/肾脏)。持续血精提示双侧附睾切除术,确认乳头状囊腺瘤。本病例为非典型的vhl相关附睾囊腺瘤,需要手术治疗,而这些良性病变通常采用保守治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
VON Hippel-Lindau syndrome: A rare case of epididymal cystadenoma associated with hemospermia
Von Hippel-Lindau (VHL) disease can cause epididymal cystadenomas, typically asymptomatic. We report a 27-year-old male with a VHL history (resected CNS hemangioblastoma) presenting unusually with recurrent hemospermia and bilateral epididymal enlargement. Ultrasound and CT confirmed bilateral epididymal lesions and other VHL-associated findings (pancreatic/renal). Persistent hemospermia prompted bilateral epididymectomy, confirming papillary cystadenomas. This case highlights an atypical, symptomatic presentation of VHL-related epididymal cystadenoma requiring surgical intervention, contrasting with usual conservative management for these benign lesions.
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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