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成人血尿患者偶然诊断为持续性苗勒管综合征:一例报告

Fortuitous Persistent Müllerian Duct Syndrome Diagnosis in an Adult Patient With Hematuria: A Case Report.

作者信息

Boitsios Alexi, Schick Tobias, Brawermann Romane, Buggenhout Alexis

机构信息

Department of Colorectal Surgery Hôpital Universitaire de Bruxelles (HUB) Brussels Belgium.

出版信息

Clin Case Rep. 2025 Sep 3;13(9):e70836. doi: 10.1002/ccr3.70836. eCollection 2025 Sep.

Abstract

Persistent Müllerian duct syndrome is a genetic disorder. It consists of Müllerian duct remains due to improper anti-Müllerian hormone. Early life presentation is often associated with undescended testes or inguinal hernias. Late diagnosis is rarer and poses a diagnostic challenge. We present a case of robotically treated PMDS in an adult who presented with hematuria.

摘要

持续性苗勒管综合征是一种遗传性疾病。它是由于抗苗勒管激素异常导致苗勒管残留所致。早期临床表现常与隐睾或腹股沟疝有关。晚期诊断较为罕见,且具有诊断挑战性。我们报告一例成年患者因血尿接受机器人手术治疗的持续性苗勒管综合征病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaeb/12406170/0440c3b7fc61/CCR3-13-e70836-g005.jpg

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