Tubular anal duplication--experiences with two cases.

T Arai, T Miyano, M Tanno, S Kohno, Y Hamasaki
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引用次数: 7

Abstract

Anal duplication is a very rare abnormality, especially in infants. Two cases of tubular anal duplication of the infant and neonate are reported in this paper. In all cases, removal of the duplicated anus through the perineal approach was accomplished without difficulty. The histology revealed a squamous epithelium with smooth muscle component around the cavity, combined with collumnar or transitional epithelium. There was no evidence of inflammation. The postoperative courses were uneventful with satisfactory anal function. The definite aetiology of this condition is still unknown, although several hypotheses have been proposed.

管状肛门重复,两个病例的经验。
肛门重复是非常罕见的异常,特别是在婴儿中。本文报告两例婴幼儿管状肛管重复。所有病例均顺利通过会阴入路切除重复肛门。组织学显示在腔周围有平滑肌成分的鳞状上皮,并有柱状或移行上皮。没有炎症的迹象。术后过程顺利,肛门功能良好。这种情况的确切病因尚不清楚,尽管已经提出了几种假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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