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Plasma Cell Leukemia: A Review of 3 Cases Managed in Kenya

Plasma Cell Leukemia (PCL) is a rare and aggressive form of plasma cell dyscrasia that can arise either de novo (primary plasma cell leukemia) or evolve from previously diagnosed and treated multiple myeloma (secondary PCL). We highlight three clinical cases with very different presentations as a re...

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Detalles Bibliográficos
Autores principales: Ong'ondi, Matilda, Kagotho, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363435/
https://www.ncbi.nlm.nih.gov/pubmed/34395001
http://dx.doi.org/10.1155/2021/4843818
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author Ong'ondi, Matilda
Kagotho, Elizabeth
author_facet Ong'ondi, Matilda
Kagotho, Elizabeth
author_sort Ong'ondi, Matilda
collection PubMed
description Plasma Cell Leukemia (PCL) is a rare and aggressive form of plasma cell dyscrasia that can arise either de novo (primary plasma cell leukemia) or evolve from previously diagnosed and treated multiple myeloma (secondary PCL). We highlight three clinical cases with very different presentations as a reminder of this diagnosis. The cases also highlight the diversity and variability that cover a patient's journey that is highly dependent on accessibility based on financial capability and social support. The clinical presentation is more aggressive due to the higher tumour burden and more proliferative tumor cells with cytopenias being profound and more organomegaly. The diagnosis is made based on at least 20% of total white blood cells being circulating plasma cells with a peripheral blood absolute plasma cell count of at least 2 × 10(9)/l. Treatment with novel agents followed by autologous stem cell transplant in those who are transplant eligible leads to better outcomes.
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spelling pubmed-83634352021-08-14 Plasma Cell Leukemia: A Review of 3 Cases Managed in Kenya Ong'ondi, Matilda Kagotho, Elizabeth Case Rep Hematol Case Report Plasma Cell Leukemia (PCL) is a rare and aggressive form of plasma cell dyscrasia that can arise either de novo (primary plasma cell leukemia) or evolve from previously diagnosed and treated multiple myeloma (secondary PCL). We highlight three clinical cases with very different presentations as a reminder of this diagnosis. The cases also highlight the diversity and variability that cover a patient's journey that is highly dependent on accessibility based on financial capability and social support. The clinical presentation is more aggressive due to the higher tumour burden and more proliferative tumor cells with cytopenias being profound and more organomegaly. The diagnosis is made based on at least 20% of total white blood cells being circulating plasma cells with a peripheral blood absolute plasma cell count of at least 2 × 10(9)/l. Treatment with novel agents followed by autologous stem cell transplant in those who are transplant eligible leads to better outcomes. Hindawi 2021-07-27 /pmc/articles/PMC8363435/ /pubmed/34395001 http://dx.doi.org/10.1155/2021/4843818 Text en Copyright © 2021 Matilda Ong'ondi and Elizabeth Kagotho. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ong'ondi, Matilda
Kagotho, Elizabeth
Plasma Cell Leukemia: A Review of 3 Cases Managed in Kenya
title Plasma Cell Leukemia: A Review of 3 Cases Managed in Kenya
title_full Plasma Cell Leukemia: A Review of 3 Cases Managed in Kenya
title_fullStr Plasma Cell Leukemia: A Review of 3 Cases Managed in Kenya
title_full_unstemmed Plasma Cell Leukemia: A Review of 3 Cases Managed in Kenya
title_short Plasma Cell Leukemia: A Review of 3 Cases Managed in Kenya
title_sort plasma cell leukemia: a review of 3 cases managed in kenya
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363435/
https://www.ncbi.nlm.nih.gov/pubmed/34395001
http://dx.doi.org/10.1155/2021/4843818
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