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[辛纳综合征的外科治疗]

[Surgical treatment of Zinner syndrome].

作者信息

Kamalov A A, Karpov V K, Pshihachev A M, Andreytsev I L, Takhirzade T B, Ekhoyan M M, Gevorkyan Z A

机构信息

Department of Urology and Andrology, Faculty of Fundamental Medicine of Moscow State University by Lomonosov, Moscow, Russia.

Medical Scientific and Educational Center of Lomonosov Moscow State University, Moscow, Russia.

出版信息

Urologiia. 2022 Sep(4):60-62.

Abstract

Zinners syndrome (SC) is a rare congenital disease characterized by ejaculatory duct obstruction, seminal vesicle cyst in combination with ipsilateral renal agenesis. This syndrome is due to development arrest of the Wolffian duct (mesonephros). Before the onset of sexual activity, the disease is asymptomatic. The main symptoms are nonspecific, including dysuria, urinary frequency, perineal and scrotal pain after ejaculation. A clinical case with the presentation of our own experience of surgical robot-assisted treatment of a patient with Zinners syndrome is presented in the article.

摘要

津纳综合征(SC)是一种罕见的先天性疾病,其特征为射精管梗阻、精囊囊肿并伴有同侧肾缺如。该综合征是由于中肾管(中肾)发育停滞所致。在性活动开始前,该病无症状。主要症状不具特异性,包括排尿困难、尿频、射精后会阴及阴囊疼痛。本文介绍了一例我们采用手术机器人辅助治疗津纳综合征患者的临床病例及自身经验。

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