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OEIS综合征患者的胃肠道重建及预后

Gastrointestinal reconstruction and outcomes for patients with the OEIS complex.

作者信息

Sawaya David, Gearhart John P

机构信息

Department of General Surgery, Division of Pediatric Surgery, University of Mississippi Medical Center, Jackson, MS 39216, USA.

出版信息

Semin Pediatr Surg. 2011 May;20(2):123-5. doi: 10.1053/j.sempedsurg.2010.12.008.

DOI:10.1053/j.sempedsurg.2010.12.008
PMID:21453858
Abstract

The OEIS complex (ie, omphalocele-exstrophy-imperforate anus-spinal defects) is a rare and complex anomaly requiring collaboration among multiple pediatric surgical subspecialties throughout the early childhood period. Initial gastrointestinal management involves identification of all intestinal components with reconstruction of the entire length of intestines in-line leading to an end colostomy. Candidacy for an abdominoperineal intestinal pull-through procedure is dependent upon the patient's ability to form solid stools, degree of pelvic neuromuscular development, and ability to comply with a bowel management program.

摘要

OEIS综合征(即脐膨出-泄殖腔外翻-肛门闭锁-脊柱裂)是一种罕见且复杂的先天性畸形,在儿童早期需要多个小儿外科亚专业共同协作。最初的胃肠道处理包括识别所有肠道组件,并将整个肠道长度进行原位重建,最终进行末端结肠造口术。腹会阴经肛门拖出术的适应证取决于患者形成成形粪便的能力、盆腔神经肌肉发育程度以及遵守肠道管理计划的能力。

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Re: Urological outcomes in the omphalocele exstrophy imperforate anus spinal defects (OEIS) complex: experience with 80 patients.关于:脐膨出-膀胱外翻-肛门闭锁-脊柱裂(OEIS)综合征的泌尿外科治疗结果:80例患者的经验
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Urological outcomes in the omphalocele exstrophy imperforate anus spinal defects (OEIS) complex: experience with 80 patients.脐膨出-膀胱外翻-肛门闭锁-脊柱裂(OEIS)复合畸形的泌尿系统结局:80 例患者的经验。
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Cloacal Exstrophy Associated with a Hindgut Duplication Anomaly: A Case Report of Challenges in Hindgut Preservation.与后肠重复畸形相关的泄殖腔外翻:后肠保留挑战的病例报告
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Hindgut Duplication in an Infant with Omphalocele-Exstrophy-Imperforate Anus-Spinal Defects (OEIS) Complex.患有脐膨出-膀胱外翻-肛门闭锁-脊柱裂(OEIS)综合征的婴儿的后肠重复畸形。
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