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Congenital pouch colon: an unusual histological finding

机译:先天性小袋结肠:不寻常的组织学发现

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Congenital pouch colon (CPC) is an unusual abnormality in which the colon ends in a pouch-like dilatation and there is generally an associated anorectal malformation. The condition varies from complete absence of normal colon to a nearly normal length of proximal colon with only recto-sigmoid involvement. There is a paucity of data on histological findings in cases of pouch colon. Resected specimens of five cases of CPC were taken. Microscopic sections were stained for H&E and Masson’s trichrome stains. We present here an interesting histological finding, namely an unusual muscle layer, inner to the circular muscle layer, in five cases of complete or almost complete CPC and discuss the clinical significance of this finding.
机译:先天性小袋结肠(CPC)是一种异常的异常,其中结肠以小袋状扩张的形式结束,通常会伴有肛门直肠畸形。从完全没有正常结肠到只有直肠乙状结肠受累的近端结肠长度接近正常,情况有所不同。袋状结肠病例的组织学发现数据很少。切除5例CPC的标本。显微镜下的切片进行了H&E和Masson的三色染色。我们在这里介绍了一个有趣的组织学发现,即在5例完全或几乎完全CPC的情况下,环形肌层内部有异常的肌层,并讨论了该发现的临床意义。

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