Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.16/2182
Title: Infantile myofibromatosis - a clinical and pathological diagnostic challenge
Author: Mota, F.
Machado, S.
Moreno, F.
Barbosa, T.
Selores, M.
Keywords: infantile myofibromatosis
mesenchymal tumor
infancy
Issue Date: 15-Apr-2017
Publisher: University of California, Davis
Citation: Dermatol Online J. 2017 Apr 15;23(4)
Abstract: Infantile myofibromatosis is a rare disorder of fibroblastic/myofibroblastic proliferation and represents the most frequent type of mesenchymal tumor in the neonatal period and primary infancy.Three clinical types have been described: solitary, multicentric, and generalized (with visceral involvement). A correct characterization of the histopathology is essential to diagnose these neoplasias in early infancy. We present a case of multicentric infantile myofibromatosis with regression over time.
Peer review: yes
URI: http://hdl.handle.net/10400.16/2182
DOI: pii: 13030/qt4493x33g
ISSN: 1087-2108
Publisher Version: http://escholarship.org/uc/item/4493x33g
Appears in Collections:SPM - Artigos publicados em revistas indexadas na Medline
SAP - Artigos publicados em revistas indexadas na Medline
SD - Artigos publicados em revistas indexadas na Medline

Files in This Item:
File Description SizeFormat 
Infantile myofibromatosis.pdf983,63 kBAdobe PDFView/Open


FacebookTwitterDeliciousLinkedInDiggGoogle BookmarksMySpace
Formato BibTex MendeleyEndnote Degois 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.