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A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report

机译:伴发隐睾和肛门闭锁的会阴错构瘤罕见病例:病例报告

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A full-term male neonate with anorectal anomaly and external perineal anomalies was referred to our service. Physical examination showed an epithelized perineal mass with cutaneous orifices, which had urine fistulization, hipotrofic perineal musculature, bilateral congenital clubfoot, hipospadic urethra, criptorquidy bilateral with nonpalpable testis and imperforate anus. A colostomy was constructed immediately after birth. The child underwent excision of perineal mass, bilateral orchidopexy, Duplay neourethroplasty and coloanal anastomosis at 3 months of age. The histopathological examination of the perineal mass revealed a hamartoma.
机译:足月男儿肛门直肠异常和会阴外异常被推荐给我们。体格检查显示会阴部上皮肿块,皮肤有小孔,有尿瘘,肥大性会阴肌肉,双侧先天性马蹄内翻足,马蹄形尿道,双侧ip不稳,睾丸无痛和肛门无孔。出生后立即进行结肠造口术。该孩子在3个月大时接受了会阴肿块切除,双侧睾丸切除,Duplay尿道成形术和结肠吻合术。会阴部肿块的组织病理学检查发现错构瘤。

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