Secondary Hemophagocytic Syndrome Associated with Richter’s Transformation in Chronic Lymphocytic Leukemia

Hemophagocytic syndrome (HPS) is an extremely rare condition arising from the overactivation of one’s own immune system. It results in excessive inflammation and tissue destruction. Prompt initiation of treatment is warranted in either scenario in order to decrease mortality. Most cases are triggere...

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Main Authors: Nura El-Haj, Wilson I. Gonsalves, Vinay Gupta, Jacob P. Smeltzer, Sameer A. Parikh, Preet P. Singh, Naseema Gangat
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/2014/287479
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author Nura El-Haj
Wilson I. Gonsalves
Vinay Gupta
Jacob P. Smeltzer
Sameer A. Parikh
Preet P. Singh
Naseema Gangat
author_facet Nura El-Haj
Wilson I. Gonsalves
Vinay Gupta
Jacob P. Smeltzer
Sameer A. Parikh
Preet P. Singh
Naseema Gangat
author_sort Nura El-Haj
collection DOAJ
description Hemophagocytic syndrome (HPS) is an extremely rare condition arising from the overactivation of one’s own immune system. It results in excessive inflammation and tissue destruction. Prompt initiation of treatment is warranted in either scenario in order to decrease mortality. Most cases are triggered by infectious agents, malignancy, or drugs. We describe the first case of a CLL patient presenting with HPS due to acquisition of EBV-related large cell lymphoma in the setting of profound immunodeficiency.
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institution Kabale University
issn 2090-6560
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publishDate 2014-01-01
publisher Wiley
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series Case Reports in Hematology
spelling doaj-art-3a7d9ac1c7964c54aaaedbcd734d63a72025-02-03T05:48:12ZengWileyCase Reports in Hematology2090-65602090-65792014-01-01201410.1155/2014/287479287479Secondary Hemophagocytic Syndrome Associated with Richter’s Transformation in Chronic Lymphocytic LeukemiaNura El-Haj0Wilson I. Gonsalves1Vinay Gupta2Jacob P. Smeltzer3Sameer A. Parikh4Preet P. Singh5Naseema Gangat6Trinity College, Dublin, IrelandDepartment of Hematology, Mayo Clinic Rochester, 200 1st Street SW, Rochester, MN 55905, USADepartment of Hematology, Mayo Clinic Rochester, 200 1st Street SW, Rochester, MN 55905, USADepartment of Hematology, Mayo Clinic Rochester, 200 1st Street SW, Rochester, MN 55905, USADepartment of Hematology, Mayo Clinic Rochester, 200 1st Street SW, Rochester, MN 55905, USADepartment of Hematology, Mayo Clinic Rochester, 200 1st Street SW, Rochester, MN 55905, USADepartment of Hematology, Mayo Clinic Rochester, 200 1st Street SW, Rochester, MN 55905, USAHemophagocytic syndrome (HPS) is an extremely rare condition arising from the overactivation of one’s own immune system. It results in excessive inflammation and tissue destruction. Prompt initiation of treatment is warranted in either scenario in order to decrease mortality. Most cases are triggered by infectious agents, malignancy, or drugs. We describe the first case of a CLL patient presenting with HPS due to acquisition of EBV-related large cell lymphoma in the setting of profound immunodeficiency.http://dx.doi.org/10.1155/2014/287479
spellingShingle Nura El-Haj
Wilson I. Gonsalves
Vinay Gupta
Jacob P. Smeltzer
Sameer A. Parikh
Preet P. Singh
Naseema Gangat
Secondary Hemophagocytic Syndrome Associated with Richter’s Transformation in Chronic Lymphocytic Leukemia
Case Reports in Hematology
title Secondary Hemophagocytic Syndrome Associated with Richter’s Transformation in Chronic Lymphocytic Leukemia
title_full Secondary Hemophagocytic Syndrome Associated with Richter’s Transformation in Chronic Lymphocytic Leukemia
title_fullStr Secondary Hemophagocytic Syndrome Associated with Richter’s Transformation in Chronic Lymphocytic Leukemia
title_full_unstemmed Secondary Hemophagocytic Syndrome Associated with Richter’s Transformation in Chronic Lymphocytic Leukemia
title_short Secondary Hemophagocytic Syndrome Associated with Richter’s Transformation in Chronic Lymphocytic Leukemia
title_sort secondary hemophagocytic syndrome associated with richter s transformation in chronic lymphocytic leukemia
url http://dx.doi.org/10.1155/2014/287479
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