| Literature DB >> 32958553 |
Arunmozhimaran Elavarasi1, Rohit Bhatia2, Sudheer Arava3, Lalit Kumar4.
Abstract
Primary leptomeningeal lymphomatosis is a rare disease with only a few hundred cases reported. We present a patient with a relatively short history of 25 days of headache followed by diplopia who was found to have primary leptomeningeal T-cell lymphoma without evidence of systemic lymphoma. The patient responded well to chemotherapy along with intrathecal medication and cranial irradiation and returned to a completely normal state of health. Not all chronic meningitis is due to infection or self-limiting inflammatory causes. It is important to consider lymphoma as a differential even in the absence of constitutional features such as loss of weight, appetite, night sweats, lymphadenopathy or hepatosplenomegaly. T-cell lymphoma with only Central Nervous system (CNS) involvement is a rare cause of chronic meningitis, which is eminently amenable to treatment and is fatal if missed. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: neurology; neurooncology
Mesh:
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Year: 2020 PMID: 32958553 PMCID: PMC7507331 DOI: 10.1136/bcr-2020-236491
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X