Congenital Localized Multiple Fibromatosis: A Case Report

Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/15340

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DC Field	Value	Language
dc.contributor.author	Palungwachira P.
dc.contributor.author	Shirai M.
dc.contributor.author	Iwahara K.
dc.contributor.author	Ogawa H.
dc.date.accessioned	2021-04-05T04:33:35Z	-
dc.date.available	2021-04-05T04:33:35Z	-
dc.date.issued	1998
dc.identifier.issn	1252208
dc.identifier.other	2-s2.0-2542633636
dc.identifier.uri	https://ir.swu.ac.th/jspui/handle/123456789/15340	-
dc.identifier.uri	https://www.scopus.com/inward/record.uri?eid=2-s2.0-2542633636&partnerID=40&md5=06260abb593edcbf5cf59fd80afc4377
dc.description.abstract	Clinical, histopathologic and electronmicroscopic findings in a case of congenital localized multiple fibromatosis of interscapular region are presented. This 10 year-old Japanese girl developed this lesion since she was 3 weeks old, metastases have never been observed. The histological and electron-microscopic features point to the hamartomous origin of this tumor with partial differentiation of its cells towards myofibroblasts and atypical fibroblasts. The differential diagnosis from other soft tissue tumors in infancy and early childhood is discussed.
dc.title	Congenital Localized Multiple Fibromatosis: A Case Report
dc.type	Article
dc.rights.holder	Scopus
dc.identifier.bibliograpycitation	Journal of the Medical Association of Thailand. Vol 81, No.5 (1998), p.370-377
Appears in Collections:	Scopus 1983-2021

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