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Leptomeningeal metastasis in a marginal zone lymphoma, presenting as a delirium: case report
BACKGROUND: Hematologic malignancies can spread to the central nervous system (CNS), either as focal lesions or as leptomeningeal disease. Marginal zone lymphoma (MZL) is a low-grade non-Hodgkin lymphoma and generally presents as an indolent disease. This case report illustrates an unexpected diagno...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7298837/ https://www.ncbi.nlm.nih.gov/pubmed/32552693 http://dx.doi.org/10.1186/s12877-020-01608-6 |
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author | Dreessen, Lisa Maréchal, Nicolas Verheyden, Michel De Becker, Ann Jochmans, Kristin Vanderhasselt, Tim Bravenboer, Bert Beyer, Ingo |
author_facet | Dreessen, Lisa Maréchal, Nicolas Verheyden, Michel De Becker, Ann Jochmans, Kristin Vanderhasselt, Tim Bravenboer, Bert Beyer, Ingo |
author_sort | Dreessen, Lisa |
collection | PubMed |
description | BACKGROUND: Hematologic malignancies can spread to the central nervous system (CNS), either as focal lesions or as leptomeningeal disease. Marginal zone lymphoma (MZL) is a low-grade non-Hodgkin lymphoma and generally presents as an indolent disease. This case report illustrates an unexpected diagnosis of leptomeningeal metastasis in an MZL, presenting as a delirium without B symptoms, pronounced hematologic progression or abnormalities on cerebral imaging. CASE PRESENTATION: An 80-year-old patient with a medical history of monoclonal B-cell lymphocytosis (MBL) with a clone indicative for an MZL, presented to the emergency and the geriatric departments with a recent cognitive deterioration and behavioral changes. MMSE score was 18/30. After excluding the most common etiologies through classical work-up including a normal head magnetic resonance imaging, a lumbar puncture was performed. In the cerebrospinal fluid an elevated protein level and increased lymphocyte count were identified, whereas beta-amyloid and tau protein levels were normal. Immunophenotyping of the lymphocytes confirmed CNS invasion by the MZL clone. Staging revealed mild splenomegaly. Prednisolone, intrathecal and systemic chemotherapy were initiated, leading to quick cognitive improvement with a final MMSE score of 28/30. CONCLUSIONS: To the best of our knowledge a delirium in an older patient due to leptomeningeal disease in MZL has never been described. To date, rare reports of CNS invasion by MZL describe focal intracranial lesions. After exclusion of common etiologies, physicians should remain vigilant when confronted with a patient with history of MBL presenting neurological symptoms. This case illustrates the importance of low threshold for lumbar punctures in this population, also for those patients with normal imaging studies. |
format | Online Article Text |
id | pubmed-7298837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72988372020-06-17 Leptomeningeal metastasis in a marginal zone lymphoma, presenting as a delirium: case report Dreessen, Lisa Maréchal, Nicolas Verheyden, Michel De Becker, Ann Jochmans, Kristin Vanderhasselt, Tim Bravenboer, Bert Beyer, Ingo BMC Geriatr Case Report BACKGROUND: Hematologic malignancies can spread to the central nervous system (CNS), either as focal lesions or as leptomeningeal disease. Marginal zone lymphoma (MZL) is a low-grade non-Hodgkin lymphoma and generally presents as an indolent disease. This case report illustrates an unexpected diagnosis of leptomeningeal metastasis in an MZL, presenting as a delirium without B symptoms, pronounced hematologic progression or abnormalities on cerebral imaging. CASE PRESENTATION: An 80-year-old patient with a medical history of monoclonal B-cell lymphocytosis (MBL) with a clone indicative for an MZL, presented to the emergency and the geriatric departments with a recent cognitive deterioration and behavioral changes. MMSE score was 18/30. After excluding the most common etiologies through classical work-up including a normal head magnetic resonance imaging, a lumbar puncture was performed. In the cerebrospinal fluid an elevated protein level and increased lymphocyte count were identified, whereas beta-amyloid and tau protein levels were normal. Immunophenotyping of the lymphocytes confirmed CNS invasion by the MZL clone. Staging revealed mild splenomegaly. Prednisolone, intrathecal and systemic chemotherapy were initiated, leading to quick cognitive improvement with a final MMSE score of 28/30. CONCLUSIONS: To the best of our knowledge a delirium in an older patient due to leptomeningeal disease in MZL has never been described. To date, rare reports of CNS invasion by MZL describe focal intracranial lesions. After exclusion of common etiologies, physicians should remain vigilant when confronted with a patient with history of MBL presenting neurological symptoms. This case illustrates the importance of low threshold for lumbar punctures in this population, also for those patients with normal imaging studies. BioMed Central 2020-06-17 /pmc/articles/PMC7298837/ /pubmed/32552693 http://dx.doi.org/10.1186/s12877-020-01608-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Dreessen, Lisa Maréchal, Nicolas Verheyden, Michel De Becker, Ann Jochmans, Kristin Vanderhasselt, Tim Bravenboer, Bert Beyer, Ingo Leptomeningeal metastasis in a marginal zone lymphoma, presenting as a delirium: case report |
title | Leptomeningeal metastasis in a marginal zone lymphoma, presenting as a delirium: case report |
title_full | Leptomeningeal metastasis in a marginal zone lymphoma, presenting as a delirium: case report |
title_fullStr | Leptomeningeal metastasis in a marginal zone lymphoma, presenting as a delirium: case report |
title_full_unstemmed | Leptomeningeal metastasis in a marginal zone lymphoma, presenting as a delirium: case report |
title_short | Leptomeningeal metastasis in a marginal zone lymphoma, presenting as a delirium: case report |
title_sort | leptomeningeal metastasis in a marginal zone lymphoma, presenting as a delirium: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7298837/ https://www.ncbi.nlm.nih.gov/pubmed/32552693 http://dx.doi.org/10.1186/s12877-020-01608-6 |
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