Avoidance of surgery for head and neck infantile myofibromatosis using imatinib monotherapy.
Prasanth PattisapuTara L WengerJohn P DahlRandall A BlyJulianna Bonilla-VelezNatalie WuAnurekha HallErin R RudzinskiJonathan A PerkinsPublished in: Clinical case reports (2022)
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.
Keyphrases
- chronic myeloid leukemia
- end stage renal disease
- newly diagnosed
- healthcare
- ejection fraction
- minimally invasive
- chronic kidney disease
- combination therapy
- clinical trial
- coronary artery bypass
- randomized controlled trial
- stem cells
- coronary artery disease
- copy number
- bone marrow
- patient reported outcomes
- mesenchymal stem cells
- patient reported