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Infantile myofibromatosis - a clinical and pathological diagnostic challenge

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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)

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