Lymphomatous meningitis


Published: June 3, 2009
Abstract Views: 393
PDF: 2746
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Authors

Malignant meningitis is a rare but devastating complication of neoplastic disease. It occurs most commonly in lung, melanoma, breast, primary brain tumours and haematological disorders. It is almost always a diffuse process even when it appears to be limited. The outcome is almost always fatal. Lymphomatous meningitis is generally accepted to occur in about 5% of diffuse large B-cell lymphomas, though rarely at presentation, it is more usual at relapse. The incidence is much higher in Burkitt’s, HIV associated lymphoma, HTLV-1 associated lymphoma, PTLDs and lymphoblastic lymphoma. There is disagreement as to those patients at risk of developing lymphomatous meningitis who may merit prophylaxis. There is a view that all lymphoma patients with a high IPI score are at risk, whilst others have attempted to identify involvement of specific extra-nodal sites such as bone marrow, breast, testicular or the gastro-intestinal tract. It is generally agreed that patients with widespread disease and high serum lactate dehydrogenase levels are at greatest risk.

Supporting Agencies


Hatton, C. (2009). Lymphomatous meningitis. Hematology Meeting Reports (formerly Haematologica Reports), 1(8). https://doi.org/10.4081/hmr.v1i8.303

Downloads

Citations