| Literature DB >> 16217262 |
Yusuke Shiozawa1, Nobutaka Kiyokawa, Junya Fujimura, Kyoko Suzuki, Yukiko Yarita, Junichiro Fujimoto, Masahiro Saito, Yuichiro Yamashiro.
Abstract
Primary lymphoma of the central nervous system (PCNSL) is extremely rare, especially in childhood. A 9-year-old Japanese boy was diagnosed as having precursor-B cell-type lymphoblastic lymphoma, based on morphologic and immunocytochemical analysis of mononuclear cells in the cerebrospinal fluid and a positive reaction for terminal deoxynucleotidyl transferase (TdT), CD19, CD79a, and CD179b. After seven courses of chemotherapy and craniospinal radiotherapy, the patient is alive, well, and in continuous complete remission. Despite its rarity, PCNSL should be included in the differential diagnosis in the presence of symptoms of increased intracranial pressure and/or unusual imaging findings of the brain.Entities:
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Year: 2005 PMID: 16217262 DOI: 10.1097/01.mph.0000184570.70222.c5
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289