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Lytic Bone Lesion: An Unusual Presentation of Hairy Cell Leukemia
Hairy cell leukemia (HCL) is a seldom encountered malignancy of lymphocytes with a low incidence in the United States. HCL generally follows an indolent course and not all patients require treatment. Most patients are asymptomatic at the time of diagnosis. Treatment is reserved for those with anemia...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920237/ https://www.ncbi.nlm.nih.gov/pubmed/33659114 http://dx.doi.org/10.7759/cureus.12959 |
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author | Fasulo, Sydney M Narvaneni, Spandana Kumar, Vinod Manje Gowda, Anusha Sultana, Yasmeen |
author_facet | Fasulo, Sydney M Narvaneni, Spandana Kumar, Vinod Manje Gowda, Anusha Sultana, Yasmeen |
author_sort | Fasulo, Sydney M |
collection | PubMed |
description | Hairy cell leukemia (HCL) is a seldom encountered malignancy of lymphocytes with a low incidence in the United States. HCL generally follows an indolent course and not all patients require treatment. Most patients are asymptomatic at the time of diagnosis. Treatment is reserved for those with anemia, thrombocytopenia, neutropenia, recurrent infections, symptomatic splenomegaly, or lymphadenopathy impairing vital organ function. Purine analogs are the mainstay of treatment with a durable response. We report a case of a 49-year old Ukrainian male who presented with bone pain secondary to a lytic bone lesion who was diagnosed with HCL. |
format | Online Article Text |
id | pubmed-7920237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-79202372021-03-02 Lytic Bone Lesion: An Unusual Presentation of Hairy Cell Leukemia Fasulo, Sydney M Narvaneni, Spandana Kumar, Vinod Manje Gowda, Anusha Sultana, Yasmeen Cureus Radiology Hairy cell leukemia (HCL) is a seldom encountered malignancy of lymphocytes with a low incidence in the United States. HCL generally follows an indolent course and not all patients require treatment. Most patients are asymptomatic at the time of diagnosis. Treatment is reserved for those with anemia, thrombocytopenia, neutropenia, recurrent infections, symptomatic splenomegaly, or lymphadenopathy impairing vital organ function. Purine analogs are the mainstay of treatment with a durable response. We report a case of a 49-year old Ukrainian male who presented with bone pain secondary to a lytic bone lesion who was diagnosed with HCL. Cureus 2021-01-28 /pmc/articles/PMC7920237/ /pubmed/33659114 http://dx.doi.org/10.7759/cureus.12959 Text en Copyright © 2021, Fasulo et al. http://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 | Radiology Fasulo, Sydney M Narvaneni, Spandana Kumar, Vinod Manje Gowda, Anusha Sultana, Yasmeen Lytic Bone Lesion: An Unusual Presentation of Hairy Cell Leukemia |
title | Lytic Bone Lesion: An Unusual Presentation of Hairy Cell Leukemia |
title_full | Lytic Bone Lesion: An Unusual Presentation of Hairy Cell Leukemia |
title_fullStr | Lytic Bone Lesion: An Unusual Presentation of Hairy Cell Leukemia |
title_full_unstemmed | Lytic Bone Lesion: An Unusual Presentation of Hairy Cell Leukemia |
title_short | Lytic Bone Lesion: An Unusual Presentation of Hairy Cell Leukemia |
title_sort | lytic bone lesion: an unusual presentation of hairy cell leukemia |
topic | Radiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920237/ https://www.ncbi.nlm.nih.gov/pubmed/33659114 http://dx.doi.org/10.7759/cureus.12959 |
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