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Split notochord syndrome with prolapsed congenital colostomy.

作者信息

Kiristioglu I, Teitelbaum D H, Dogruyol H

机构信息

CS Mott Children's Hospital and the University of Michigan Medical Center, Ann Arbor 48109-0245, USA.

出版信息

J Pediatr Surg. 1998 Mar;33(3):525-8. doi: 10.1016/s0022-3468(98)90105-1.

DOI:10.1016/s0022-3468(98)90105-1
PMID:9537574
Abstract

A case of split notochord syndrome associated with a prolapsed colostomylike dorsal enteric opening, a foreshortened colon, imperforate anus, and meningocele is presented. The surgical management of this disorder is discussed and available literature is reviewed. The patient was successfully treated with a combined, single-stage surgical correction.

摘要

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A case of split notochord syndrome with congenital ileal atresia, the total absence of a colon, and a dorsal enteric cyst communicating to the retroperitoneal isolated ceca with a vesical fistula.一例合并先天性回肠闭锁、结肠完全缺如及背侧肠囊肿并与经膀胱瘘与腹膜后孤立盲肠相通的分裂脊索综合征病例。
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