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Article

Late Relapse in Genetically Determined Infantile Myofibromatosis. A Case Report and Brief Focus on Recurrences.

Journal of pediatric hematology/oncology - 1 Oct 2024

Conte Alessio, De Padova Damiana, Giglio Serena, Livellara Virginia, Manzitti Carla, De Marco Patrizia, Capra Valeria, Sorrentino Stefania

Abstract excerpt

BACKGROUND: Infantile myofibromatosis (IM) is a rare disorder characterized by benign tumors in the skin, subcutaneous tissue, muscle, and occasionally viscera. IM can be hereditary due to PDGFRB or NOTCH3 variants. Treatment is mainly conservative or surgical. Combination regimens have been used in case of disseminated disease. OBSERVATION: We present relapsed disease of IM 11 years after diagnosis in a...

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PMID: 39141797
DOI: 10.1097/MPH.0000000000002942

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Late Relapse in Genetically Determined Infantile Myofibromatosis. A Case Report and Brief Focus on Recurrences.PMID 39141797Read ↗

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