| Literature DB >> 30299348 |
Ayça Koca Yozgat1, Derya Ozyoruk1, Dilek Kacar1, Ibrahim I Cetin2, Inci Yaman Bajin1, Kubilay Inan3, Ayse S Oguz4.
Abstract
Burkitt lymphoma manifesting as an intracardiac mass is a rare entity. This report describes the case of a 10-year-old boy who presented with an intracardiac mass and tumor thrombosis in the anterior mediastinum that proved to be Burkitt lymphoma. The LMB-96 chemotherapy protocol was given and at the end of the treatment there was still residual mass. A biopsy was performed and the pathology revealed thymus tissue. The patient has been in complete remission for 3 months. Burkitt lymphoma has a short doubling time and an intracardiac lesion can become life threatening. Early recognition and prompt treatment are crucial in achieving optimal outcomes.Entities:
Mesh:
Year: 2019 PMID: 30299348 DOI: 10.1097/MPH.0000000000001327
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289