Posterior Cloacal Variant with Clitorolabial Transposition and a Rectoperineal Fistula.

IF 0.6 Q4 SURGERY
Niveshni Maistry, Giulia Brisighelli, Chris Westgarth-Taylor
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引用次数: 0

Abstract

We present a case and discuss the management of a posterior cloacal variant not as yet described in the literature. A 5-week-old infant presented to our institution with a posterior cloacal variant and transposition of the clitoris and labia. After initial radiological investigations, staged operative intervention was performed over a 1-year period. This included an initial laparotomy (with drainage of hydrocolpos and formation of a colostomy), a left ureteric reimplantation and a posterior sagittal anorectoplasty due to a rectoperineal fistula. The child is under continued long-term follow-up by our specialist pediatric surgical team.

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后阴囊变异性伴阴蒂移位和直肠会阴瘘。
我们提出了一个案例,并讨论了后泄殖腔变异尚未在文献中描述的管理。一个5周大的婴儿出现后阴囊变异和阴蒂和阴唇移位。在最初的放射学调查后,在1年的时间里进行了分阶段的手术干预。这包括最初的剖腹手术(引流直肠积水并形成结肠造口术),左侧输尿管再植和由于直肠会阴瘘的后矢状直肠成形术。我们的儿科外科专家团队正在对这名儿童进行持续的长期随访。
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来源期刊
自引率
33.30%
发文量
39
审稿时长
12 weeks
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