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Updated: Mar 1, 2026

Author Spotlight: Genetically Engineered Mouse Models and Pathological Characterization of Neurofibromatosis Type 1 Associated Tumors
Published on: May 17, 2024
Infantile myofibromatosis - a clinical and pathological diagnostic challenge
Fernando Mota1, Susana Machado, Filipa Moreno
1Dermatology Department, Centro Hospitalar do Porto, Porto, Portugal. fernandojrmota@gmail.com.
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.
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