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一名男性新生儿罕见的复杂会阴畸形病例:多阶段手术治疗

A rare case of complex perineal anomaly in a male neonate: Multistage surgical management.

作者信息

Houas Yasmine, Thamri Fatma, Guitouni Asma, Jouini Riadh

机构信息

Pediatric Surgery Department "A", Children Hospital Bechir Hamza, Tunis, Tunisia.

Tunis El Manar University, Tunis, Tunisia.

出版信息

Urol Case Rep. 2025 Aug 26;62:103179. doi: 10.1016/j.eucr.2025.103179. eCollection 2025 Sep.

Abstract

We present a rare case of a full-term male neonate with a complex perineal anomaly featuring a mucosa-lined cleft extending from the penile base to the right gluteal fold, accompanied by penoscrotal transposition, hemiscrotal hypoplasia, and hypospadias. The lesion's anatomical and histological characteristics suggest antenatal rupture of a rectal duplication cyst. This report highlights the diagnostic challenges of exteriorized rectal duplications and underscores the importance of multistage reconstruction for optimal functional and cosmetic outcomes.

摘要

我们报告一例罕见的足月男婴,患有复杂的会阴异常,其特征为有一条内衬黏膜的裂隙,从阴茎基部延伸至右臀皱襞,同时伴有阴茎阴囊转位、半侧阴囊发育不全和尿道下裂。该病变的解剖和组织学特征提示为直肠重复囊肿产前破裂。本报告强调了外露型直肠重复畸形的诊断挑战,并强调了多阶段重建对于实现最佳功能和美容效果的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c32/12410184/0f6bff31558b/gr1.jpg

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