Houas Yasmine, Thamri Fatma, Guitouni Asma, Jouini Riadh
Pediatric Surgery Department "A", Children Hospital Bechir Hamza, Tunis, Tunisia.
Tunis El Manar University, Tunis, Tunisia.
Urol Case Rep. 2025 Aug 26;62:103179. doi: 10.1016/j.eucr.2025.103179. eCollection 2025 Sep.
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.
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。
