Congenital peripheral primitive neuroectodermal tumor: A case treated successfully with multimodality treatment

Publication date: Available online 7 November 2014 Source:Journal of the Egyptian National Cancer Institute Author(s): Shikha Goyal , Ahitagni Biswas , Ruchika Gupta , Bidhu Kalyan Mohanti Neonatal tumors comprise less than two percent of childhood malignancies. Most are solid tumors, most common histologies being teratoma and neuroblastoma. We encountered a child who was detected to have a right arm mass on antenatal sonogram, which was diagnosed to be a primitive neuroectodermal tumor involving the triceps on fine needle aspiration cytology performed in the post-natal period. The child was successfully treated with multimodality treatment consisting of surgery, chemotherapy and radiotherapy. We also discuss briefly the problems associated with therapy in neonatal period. A review of all cases reported to have congenital Ewing’s sarcoma family of tumors is presented. Novel therapies are needed to improve efficacy and decrease the devastating side effects of treatment in this age group.
Source: Journal of the Egyptian National Cancer Institute - Category: Cancer & Oncology Source Type: research