Hemophagocytic Lymphohistiocytosis Secondary to Disseminated Histoplasmosis in Rheumatologic Disease

Background. Hemophagocytic lymphohistiocytosis (HLH) was originally described in pediatric patients presenting with fever, hepatosplenomegaly, and blood cell abnormalities. Later, HLH was recognized to occur in adults, often associated with hematologic malignancies or serious infections. Conclusion....

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Main Authors: Yael Kusne, Michael Christiansen, Christopher Conley, Juan Gea-Banacloche, Ayan Sen
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Case Reports in Critical Care
Online Access:http://dx.doi.org/10.1155/2021/6612710
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author Yael Kusne
Michael Christiansen
Christopher Conley
Juan Gea-Banacloche
Ayan Sen
author_facet Yael Kusne
Michael Christiansen
Christopher Conley
Juan Gea-Banacloche
Ayan Sen
author_sort Yael Kusne
collection DOAJ
description Background. Hemophagocytic lymphohistiocytosis (HLH) was originally described in pediatric patients presenting with fever, hepatosplenomegaly, and blood cell abnormalities. Later, HLH was recognized to occur in adults, often associated with hematologic malignancies or serious infections. Conclusion. Patients presenting with HLH are critically ill, and rapid diagnosis is key. In adults, the search for the trigger must begin promptly as time to diagnosis effects survival. The underlying trigger in our patients was Histoplasma capsulatum infection, which is rare in the southwestern United States. Prompt diagnosis led to recovery in one patient, while the other did not survive.
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series Case Reports in Critical Care
spelling doaj-art-c918ef4974b047be9f20de06a55a45282025-08-20T02:19:41ZengWileyCase Reports in Critical Care2090-64202090-64392021-01-01202110.1155/2021/66127106612710Hemophagocytic Lymphohistiocytosis Secondary to Disseminated Histoplasmosis in Rheumatologic DiseaseYael Kusne0Michael Christiansen1Christopher Conley2Juan Gea-Banacloche3Ayan Sen4Department of Internal Medicine, Mayo Clinic Arizona, Phoenix, AZ, USADepartment of Neurology, Mayo Clinic Arizona, Phoenix, AZ, USADepartment of Pathology, Mayo Clinic Arizona, Phoenix, AZ, USADepartment of Infectious Disease, Mayo Clinic Arizona, Phoenix, AZ, USADepartment of Critical Care Medicine, Mayo Clinic Arizona, Phoenix, AZ, USABackground. Hemophagocytic lymphohistiocytosis (HLH) was originally described in pediatric patients presenting with fever, hepatosplenomegaly, and blood cell abnormalities. Later, HLH was recognized to occur in adults, often associated with hematologic malignancies or serious infections. Conclusion. Patients presenting with HLH are critically ill, and rapid diagnosis is key. In adults, the search for the trigger must begin promptly as time to diagnosis effects survival. The underlying trigger in our patients was Histoplasma capsulatum infection, which is rare in the southwestern United States. Prompt diagnosis led to recovery in one patient, while the other did not survive.http://dx.doi.org/10.1155/2021/6612710
spellingShingle Yael Kusne
Michael Christiansen
Christopher Conley
Juan Gea-Banacloche
Ayan Sen
Hemophagocytic Lymphohistiocytosis Secondary to Disseminated Histoplasmosis in Rheumatologic Disease
Case Reports in Critical Care
title Hemophagocytic Lymphohistiocytosis Secondary to Disseminated Histoplasmosis in Rheumatologic Disease
title_full Hemophagocytic Lymphohistiocytosis Secondary to Disseminated Histoplasmosis in Rheumatologic Disease
title_fullStr Hemophagocytic Lymphohistiocytosis Secondary to Disseminated Histoplasmosis in Rheumatologic Disease
title_full_unstemmed Hemophagocytic Lymphohistiocytosis Secondary to Disseminated Histoplasmosis in Rheumatologic Disease
title_short Hemophagocytic Lymphohistiocytosis Secondary to Disseminated Histoplasmosis in Rheumatologic Disease
title_sort hemophagocytic lymphohistiocytosis secondary to disseminated histoplasmosis in rheumatologic disease
url http://dx.doi.org/10.1155/2021/6612710
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