| Literature DB >> 25389917 |
Meaghann S Weaver1, Fariba Navid, Alison Huppmann, Holly Meany, Anne Angiolillo.
Abstract
Although solitary presentations of infantile myofibromatosis tend toward spontaneous regression, multicentric forms fare worse. Previous case reports have depicted observation, surgical resection, and systemic therapies as treatment options. This paper reports well-tolerated, successful outcomes in a series of patients with high-risk infantile myofibromatosis in need of life-sustaining interventions treated with a combination of vincristine and dactinomycin. The clinical presentation, pathology, and radiographic findings are described.Entities:
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Year: 2015 PMID: 25389917 DOI: 10.1097/MPH.0000000000000286
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289