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pubmed-article:10910628pubmed:dateCreated1999-10-27lld:pubmed
pubmed-article:10910628pubmed:abstractTextCongenital defect of the small intestinal musculature is a rare cause of neonatal spontaneous intestinal obstruction or perforation. Its etiology and pathogenesis are still controversial. A male infant presented with intestinal obstruction at two days of age and rapidly progressed to perforation and septic shock. He died at seven days of age. Autopsy finding revealed a perforation hole at twenty-five cm proximal to ileocecal valve. Histology examination demonstrates multifocal deficiency of the inner circular muscle layer three cm around the perforation site. The clinical and histological characteristics are reviewed and discussed. We propose that the muscle defect of small intestine, especially ileum, is secondary to ischemic injury rather than an embryological malformation.lld:pubmed
pubmed-article:10910628pubmed:languageenglld:pubmed
pubmed-article:10910628pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
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pubmed-article:10910628pubmed:statusMEDLINElld:pubmed
pubmed-article:10910628pubmed:issn1608-8115lld:pubmed
pubmed-article:10910628pubmed:authorpubmed-author:HuangP CPClld:pubmed
pubmed-article:10910628pubmed:authorpubmed-author:ZarJ HJHlld:pubmed
pubmed-article:10910628pubmed:authorpubmed-author:HuangS FSFlld:pubmed
pubmed-article:10910628pubmed:authorpubmed-author:WuM ZMZlld:pubmed
pubmed-article:10910628pubmed:issnTypePrintlld:pubmed
pubmed-article:10910628pubmed:volume40lld:pubmed
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pubmed-article:10910628pubmed:pagination271-3lld:pubmed
pubmed-article:10910628pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:10910628pubmed:articleTitleNeonatal intestinal perforation caused by congenital defect of the small intestinal musculature: report of one case.lld:pubmed
pubmed-article:10910628pubmed:affiliationDepartment of Pathology, National Taiwan University Hospital, Taipei, Taiwan.lld:pubmed
pubmed-article:10910628pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10910628pubmed:publicationTypeCase Reportslld:pubmed