Michael Sabbaj, Katrina Winsnes, Mathew Geltzeiler
Sinonasal pediatric rhabdomyosarcoma is a rare cancer with a prognosis dependent on stage/grade, histology, and molecular characteristics. Radiation therapy is considered first-line therapy in conjunction with chemotherapy, determined based on the disease risk group. Surgery is generally recommended when margin-free resections are possible. Here we present a unique case report of a patient with recurrent rhabdomyosarcoma and an overview of the salient literature pertaining to the management of this case.