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Sustained response to erythropoietin for anemia in NK-cell large granular lymphocytosis: A brief case report

Large granular lymphocytic leukemia (LGL) is a rare lymphoproliferative disorder that involves the T-cell lineage in around 85% of cases and NK-cell lineage in 15%. Most patients require treatment at some point of their disease trajectory to address clinical symptomatology largely pertaining to cyto...

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Autores principales: Kwaramba, Tendai, Lewis, Brian, Burks, Bruce, Ruiz, Bernardo, Iyer, Swaminathan P., Safa, Firas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857583/
https://www.ncbi.nlm.nih.gov/pubmed/35242524
http://dx.doi.org/10.1016/j.lrr.2022.100292
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author Kwaramba, Tendai
Lewis, Brian
Burks, Bruce
Ruiz, Bernardo
Iyer, Swaminathan P.
Safa, Firas
author_facet Kwaramba, Tendai
Lewis, Brian
Burks, Bruce
Ruiz, Bernardo
Iyer, Swaminathan P.
Safa, Firas
author_sort Kwaramba, Tendai
collection PubMed
description Large granular lymphocytic leukemia (LGL) is a rare lymphoproliferative disorder that involves the T-cell lineage in around 85% of cases and NK-cell lineage in 15%. Most patients require treatment at some point of their disease trajectory to address clinical symptomatology largely pertaining to cytopenia. While immunosuppression represents the backbone of LGL therapy, there is no consensus on the best next line following failure of immunosuppression. Here we present a case of LGL-associated cytopenia in a 73-year-old male refractory to immunosuppression, treated with adjunct erythropoietin alpha (EPO) with a marked response. Our case suggests that EPO therapy may provide therapeutic benefit in refractory LGL cases when used in conjunction with immunosuppressive therapy.
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spelling pubmed-88575832022-03-02 Sustained response to erythropoietin for anemia in NK-cell large granular lymphocytosis: A brief case report Kwaramba, Tendai Lewis, Brian Burks, Bruce Ruiz, Bernardo Iyer, Swaminathan P. Safa, Firas Leuk Res Rep Article Large granular lymphocytic leukemia (LGL) is a rare lymphoproliferative disorder that involves the T-cell lineage in around 85% of cases and NK-cell lineage in 15%. Most patients require treatment at some point of their disease trajectory to address clinical symptomatology largely pertaining to cytopenia. While immunosuppression represents the backbone of LGL therapy, there is no consensus on the best next line following failure of immunosuppression. Here we present a case of LGL-associated cytopenia in a 73-year-old male refractory to immunosuppression, treated with adjunct erythropoietin alpha (EPO) with a marked response. Our case suggests that EPO therapy may provide therapeutic benefit in refractory LGL cases when used in conjunction with immunosuppressive therapy. Elsevier 2022-02-09 /pmc/articles/PMC8857583/ /pubmed/35242524 http://dx.doi.org/10.1016/j.lrr.2022.100292 Text en Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Kwaramba, Tendai
Lewis, Brian
Burks, Bruce
Ruiz, Bernardo
Iyer, Swaminathan P.
Safa, Firas
Sustained response to erythropoietin for anemia in NK-cell large granular lymphocytosis: A brief case report
title Sustained response to erythropoietin for anemia in NK-cell large granular lymphocytosis: A brief case report
title_full Sustained response to erythropoietin for anemia in NK-cell large granular lymphocytosis: A brief case report
title_fullStr Sustained response to erythropoietin for anemia in NK-cell large granular lymphocytosis: A brief case report
title_full_unstemmed Sustained response to erythropoietin for anemia in NK-cell large granular lymphocytosis: A brief case report
title_short Sustained response to erythropoietin for anemia in NK-cell large granular lymphocytosis: A brief case report
title_sort sustained response to erythropoietin for anemia in nk-cell large granular lymphocytosis: a brief case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857583/
https://www.ncbi.nlm.nih.gov/pubmed/35242524
http://dx.doi.org/10.1016/j.lrr.2022.100292
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