Mota, F.Machado, S.Moreno, F.Barbosa, T.Selores, M.2017-09-042017-09-042017-04-15Dermatol Online J. 2017 Apr 15;23(4)1087-2108http://hdl.handle.net/10400.16/2182Infantile 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.enginfantile myofibromatosismesenchymal tumorinfancyjournal articlepii: 13030/qt4493x33g