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Intravascular large B-cell lymphoma in Hispanics: a case series and literature review

Intravascular large B-cell Lymphoma (IVLBCL) is a rare subtype of extra nodal non-Hodgkin’s lymphoma, which is challenging to diagnose and has a poor prognosis. Here we describe three non-White Hispanic patients newly diagnosed with IVLBCL within 14-month period. All of them presented with persisten...

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Autores principales: Nguyen, Sonha, Pakbaz, Zahra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7599000/
https://www.ncbi.nlm.nih.gov/pubmed/33194130
http://dx.doi.org/10.1080/20009666.2020.1811073
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author Nguyen, Sonha
Pakbaz, Zahra
author_facet Nguyen, Sonha
Pakbaz, Zahra
author_sort Nguyen, Sonha
collection PubMed
description Intravascular large B-cell Lymphoma (IVLBCL) is a rare subtype of extra nodal non-Hodgkin’s lymphoma, which is challenging to diagnose and has a poor prognosis. Here we describe three non-White Hispanic patients newly diagnosed with IVLBCL within 14-month period. All of them presented with persistent fever of unknown origin and symptomatic severe anemia as the initial manifestations. Two out of three cases were successfully diagnosed in a timely manner by fat pad biopsy and have remained disease free up to 34 months after chemotherapy. The third case was diagnosed by bone marrow biopsy and deceased one week later after choosing home hospice care. To date, this is the largest published case series of IVLBCL in non-White Hispanics.
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spelling pubmed-75990002020-11-12 Intravascular large B-cell lymphoma in Hispanics: a case series and literature review Nguyen, Sonha Pakbaz, Zahra J Community Hosp Intern Med Perspect Case Report Intravascular large B-cell Lymphoma (IVLBCL) is a rare subtype of extra nodal non-Hodgkin’s lymphoma, which is challenging to diagnose and has a poor prognosis. Here we describe three non-White Hispanic patients newly diagnosed with IVLBCL within 14-month period. All of them presented with persistent fever of unknown origin and symptomatic severe anemia as the initial manifestations. Two out of three cases were successfully diagnosed in a timely manner by fat pad biopsy and have remained disease free up to 34 months after chemotherapy. The third case was diagnosed by bone marrow biopsy and deceased one week later after choosing home hospice care. To date, this is the largest published case series of IVLBCL in non-White Hispanics. Taylor & Francis 2020-10-29 /pmc/articles/PMC7599000/ /pubmed/33194130 http://dx.doi.org/10.1080/20009666.2020.1811073 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nguyen, Sonha
Pakbaz, Zahra
Intravascular large B-cell lymphoma in Hispanics: a case series and literature review
title Intravascular large B-cell lymphoma in Hispanics: a case series and literature review
title_full Intravascular large B-cell lymphoma in Hispanics: a case series and literature review
title_fullStr Intravascular large B-cell lymphoma in Hispanics: a case series and literature review
title_full_unstemmed Intravascular large B-cell lymphoma in Hispanics: a case series and literature review
title_short Intravascular large B-cell lymphoma in Hispanics: a case series and literature review
title_sort intravascular large b-cell lymphoma in hispanics: a case series and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7599000/
https://www.ncbi.nlm.nih.gov/pubmed/33194130
http://dx.doi.org/10.1080/20009666.2020.1811073
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