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Solitary intestinal fibromatosis: a rare cause of intestinal obstruction in neonate and infant.

作者信息

Chang W W, Griffith K M

机构信息

Department of Pathology, West Virginia University School of Medicine, Morgantown 26506.

出版信息

J Pediatr Surg. 1991 Dec;26(12):1406-8. doi: 10.1016/0022-3468(91)91048-4.

DOI:10.1016/0022-3468(91)91048-4
PMID:1765922
Abstract

A 5-month-old white boy infant exhibited remarkable growth retardation and subsequently developed ileal obstruction, which was found to be due to solitary intestinal fibromatosis. This rare lesion has an excellent prognosis if it is completely excised. This is in contrast to cases of congenital fibromatosis with multiple lesions, which carries a poor prognosis.

摘要

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