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Congenital Localized Multiple Fibromatosis: A Case Report

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dc.contributor.authorPalungwachira P.
dc.contributor.authorShirai M.
dc.contributor.authorIwahara K.
dc.contributor.authorOgawa H.
dc.date.accessioned2021-04-05T04:33:35Z
dc.date.available2021-04-05T04:33:35Z
dc.date.issued1998
dc.date.issuedBE2541
dc.description.abstractClinical, 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.format.mimetypeapplication/pdf
dc.identifier.citationJournal of the Medical Association of Thailand. Vol 81, No.5 (1998), p.370-377
dc.identifier.issn1252208
dc.identifier.other2-s2.0-2542633636
dc.identifier.urihttps://hdl.handle.net/20.500.14740/7249
dc.rights.holderScopus
dc.titleCongenital Localized Multiple Fibromatosis: A Case Report
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-2542633636&partnerID=40&md5=06260abb593edcbf5cf59fd80afc4377

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