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Incidental Splenic Marginal Zone Lymphoma With Extreme Macrocytosis After Hydroxyurea Use: A Case Report

Splenic marginal zone lymphoma (SMZL) is a low-grade mature B-cell lymphoma that typically presents in the form of splenomegaly and lymphocytosis. The diagnosis is traditionally made through splenic histology, the presence of circulating villous lymphocytes, or bone marrow biopsy. Its treatment can...

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Autores principales: Sultan, Kinza, Kal, Sarala, Wasson, Andrew, Farmand, Farbod
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899520/
https://www.ncbi.nlm.nih.gov/pubmed/36751210
http://dx.doi.org/10.7759/cureus.33462
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author Sultan, Kinza
Kal, Sarala
Wasson, Andrew
Farmand, Farbod
author_facet Sultan, Kinza
Kal, Sarala
Wasson, Andrew
Farmand, Farbod
author_sort Sultan, Kinza
collection PubMed
description Splenic marginal zone lymphoma (SMZL) is a low-grade mature B-cell lymphoma that typically presents in the form of splenomegaly and lymphocytosis. The diagnosis is traditionally made through splenic histology, the presence of circulating villous lymphocytes, or bone marrow biopsy. Its treatment can be in the form of chemotherapy, such as rituximab, or active surveillance. This case presentation discusses a 76-year-old female with a long history of hydroxyurea use for an unknown reason presenting with atypical symptoms requiring bone marrow biopsy to diagnose SMZL. This unique case demonstrates the importance of further research and studies into atypical SMZL presentations and hydroxyurea’s potential in precipitating secondary malignancies.
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spelling pubmed-98995202023-02-06 Incidental Splenic Marginal Zone Lymphoma With Extreme Macrocytosis After Hydroxyurea Use: A Case Report Sultan, Kinza Kal, Sarala Wasson, Andrew Farmand, Farbod Cureus Internal Medicine Splenic marginal zone lymphoma (SMZL) is a low-grade mature B-cell lymphoma that typically presents in the form of splenomegaly and lymphocytosis. The diagnosis is traditionally made through splenic histology, the presence of circulating villous lymphocytes, or bone marrow biopsy. Its treatment can be in the form of chemotherapy, such as rituximab, or active surveillance. This case presentation discusses a 76-year-old female with a long history of hydroxyurea use for an unknown reason presenting with atypical symptoms requiring bone marrow biopsy to diagnose SMZL. This unique case demonstrates the importance of further research and studies into atypical SMZL presentations and hydroxyurea’s potential in precipitating secondary malignancies. Cureus 2023-01-06 /pmc/articles/PMC9899520/ /pubmed/36751210 http://dx.doi.org/10.7759/cureus.33462 Text en Copyright © 2023, Sultan et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Sultan, Kinza
Kal, Sarala
Wasson, Andrew
Farmand, Farbod
Incidental Splenic Marginal Zone Lymphoma With Extreme Macrocytosis After Hydroxyurea Use: A Case Report
title Incidental Splenic Marginal Zone Lymphoma With Extreme Macrocytosis After Hydroxyurea Use: A Case Report
title_full Incidental Splenic Marginal Zone Lymphoma With Extreme Macrocytosis After Hydroxyurea Use: A Case Report
title_fullStr Incidental Splenic Marginal Zone Lymphoma With Extreme Macrocytosis After Hydroxyurea Use: A Case Report
title_full_unstemmed Incidental Splenic Marginal Zone Lymphoma With Extreme Macrocytosis After Hydroxyurea Use: A Case Report
title_short Incidental Splenic Marginal Zone Lymphoma With Extreme Macrocytosis After Hydroxyurea Use: A Case Report
title_sort incidental splenic marginal zone lymphoma with extreme macrocytosis after hydroxyurea use: a case report
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899520/
https://www.ncbi.nlm.nih.gov/pubmed/36751210
http://dx.doi.org/10.7759/cureus.33462
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