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Orientador(es)
Resumo(s)
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.
Descrição
Palavras-chave
infantile myofibromatosis mesenchymal tumor infancy
Contexto Educativo
Citação
Dermatol Online J. 2017 Apr 15;23(4)
Editora
University of California, Davis
