| Literature DB >> 18021474 |
Jose Ponce1, Angel Segura, Alejandra Gimenez, Roberto Diaz, Jorge Molina, Laura Palomar, Jose Gomez Codina.
Abstract
Primary meningeal lymphoma is a rare clinical entity. Central nervous system infiltration by systemic lymphoma should always be excluded. Diagnosis can be difficult, and prognosis is usually poor. Most are of B-cell origin. We present the case of a young man with a primary meningeal lymphoma of T-cell origin. He was treated with systemic chemotherapy with high-dose methotrexate and cytarabine and intraventricular chemotherapy. He had a clinical improvement and a complete remission, with a long overall survival. There is no standard treatment for this rare disease. Traditionally, treatment has been based in craniospinal radiation therapy and intrathecal chemotherapy, with poor overall results. More recently, systemic chemotherapy with high-dose methotrexate has been advocated, which could avoid the long-term toxicity of craniospinal radiation therapy, and could improve the prognosis of these patients.Entities:
Mesh:
Year: 2007 PMID: 18021474 DOI: 10.3816/clm.2007.n.041
Source DB: PubMed Journal: Clin Lymphoma Myeloma ISSN: 1557-9190