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[肠套叠的罕见病因:先天性息肉样胃异位。1例病例研究及文献复习]

[Unusual cause of intestinal invagination: congenital polypoid-form gastric heterotopia. Study of a case and review of the literature].

作者信息

Justrabo E, Michiels R, Nivelon J L, Piard F, Autissier J M, Muller F

出版信息

Arch Fr Pediatr. 1984 Jun-Jul;41(6):391-4.

PMID:6487041
Abstract

The authors report a case of polypoid heterotopic gastric mucosa in the ileum presenting as intussusception with hypochromic anemia in a 6 year-old boy. Tumorous heterotopic gastric mucosa in the small bowel is very uncommon. So far 22 similar cases have been published in the literature. This congenital intestinal anomaly is discovered in one third of the cases during the first decade. In 9 of 23 cases gastric heterotopia was diagnosed after an ileal resection for intussusception induced by the heterotopia presenting as a pedunculated or sessile polyp. In our case the great number of the polypoid formations is exceptional and has not been previously described.

摘要

作者报告了一例6岁男孩回肠息肉样异位胃黏膜,表现为肠套叠并伴有低色素性贫血。小肠肿瘤性异位胃黏膜非常罕见。迄今为止,文献中已发表了22例类似病例。这种先天性肠道异常在三分之一的病例中是在第一个十年期间发现的。在23例病例中的9例中,因异位胃黏膜导致的肠套叠表现为带蒂或无蒂息肉,在回肠切除术后诊断出胃异位。在我们的病例中,息肉样病变的数量之多是罕见的,且此前未曾有过描述。

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