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Mediastinal T-cell lymphoma in a boy 7 years after treatment of supratentorial primitive neuroectodermal tumor
Thomas Lehrnbecher1, Frank Deinlein, Alexander Marx
1Department of Pediatric Hematology and Oncology, Children's Hospital III, Frankfurt, Germany. thomas_lehrnbecher@yahoo.com
Abstract:
Medulloblastoma/primitive neuroectodermal tumor (PNET) is one of the most common central nervous system tumors in children and requires aggressive multimodality therapy. The authors describe a patient who developed mediastinal T-cell lymphoma 7 years after treatment of supratentorial PNET. Despite a good tumor response, the patient died during induction therapy because of invasive pulmonary aspergillosis. The authors conclude from this case that patients treated for medulloblastoma/PNET should be followed carefully for years. In addition, patients with second malignancies should be considered as a high-risk population for opportunistic infections.