Clinical Case Reports (Feb 2022)

Avoidance of surgery for head and neck infantile myofibromatosis using imatinib monotherapy

  • Prasanth Pattisapu,
  • Tara L. Wenger,
  • John P. Dahl,
  • Randall A. Bly,
  • Juliana Bonilla‐Velez,
  • Natalie Wu,
  • Anurekha Hall,
  • Erin R. Rudzinski,
  • Jonathan A. Perkins

DOI
https://doi.org/10.1002/ccr3.5382
Journal volume & issue
Vol. 10, no. 2
pp. n/a – n/a

Abstract

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Abstract Describe a novel use for a kinase inhibitor, imatinib, in young children with a known activated somatic mutation in PDGFR‐beta. Two patients with infantile myofibromatosis treated with imatinib. Case description of evaluation, diagnosis and treatment decisions for infantile myfibromatosis of the head and neck. Description of medical therapy for infantile myofibromatosis in these patients. For function threatening myofibromas of a known genotype, in infants, targeted medical therapy is a treatment option.

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