男性新生儿复杂会阴异常一例:多阶段手术处理

IF 0.4 Q4 UROLOGY & NEPHROLOGY
Yasmine Houas , Fatma Thamri , Asma Guitouni , Riadh Jouini
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引用次数: 0

摘要

我们报告一例罕见的足月男性新生儿,其复杂的会阴异常表现为从阴茎基部延伸至右侧臀襞的粘膜间隙,并伴有阴部转位、半阴部发育不全和尿道下裂。病变的解剖和组织学特征提示产前直肠重复囊肿破裂。本报告强调了直肠外复制的诊断挑战,并强调了多阶段重建的重要性,以获得最佳的功能和美容结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of complex perineal anomaly in a male neonate: Multistage surgical management
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.
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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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