Secondary hemophagocytic lymphohistiocytosis and isolated cerebellar ataxia due to disseminated tuberculosis with challenging management: A rare case report

Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder which occurs due to excessive immune response and high cytokine levels leading to tissue damage and organ failure. HLH can be primary and secondary. The etiology and presentation of secondary HLH remain diverse. Treatment of sec...

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Main Authors: Rahul Kumar Gupta, Sammi Pundir, Mansi Kala, Avriti Baveja, Pranshul Rawat, Anuradha Khandelwal
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2025-01-01
Series:Indian Journal of Allergy Asthma and Immunology
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Online Access:https://journals.lww.com/10.4103/ijaai.ijaai_64_24
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author Rahul Kumar Gupta
Sammi Pundir
Mansi Kala
Avriti Baveja
Pranshul Rawat
Anuradha Khandelwal
author_facet Rahul Kumar Gupta
Sammi Pundir
Mansi Kala
Avriti Baveja
Pranshul Rawat
Anuradha Khandelwal
author_sort Rahul Kumar Gupta
collection DOAJ
description Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder which occurs due to excessive immune response and high cytokine levels leading to tissue damage and organ failure. HLH can be primary and secondary. The etiology and presentation of secondary HLH remain diverse. Treatment of secondary HLH includes management of primary conditions and immunosuppressives. Several cases of secondary HLH due to tuberculosis (TB) have been reported in the past although their management beyond antitubercular therapy and follow-up was not reported. Here, we present a rare case report of secondary HLH and isolated cerebellar ataxia due to disseminated TB that responded to intravenous immunoglobulin in addition to antitubercular therapy and steroids. Patients showed complete response to therapy with normalization of hematological parameters and bone marrow findings. The patient was declared cured after 6 months of treatment.
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institution Matheson Library
issn 0972-6691
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language English
publishDate 2025-01-01
publisher Wolters Kluwer Medknow Publications
record_format Article
series Indian Journal of Allergy Asthma and Immunology
spelling doaj-art-e46eda79bcc945e6b32f5fc93cbf99992025-07-04T12:19:03ZengWolters Kluwer Medknow PublicationsIndian Journal of Allergy Asthma and Immunology0972-66912320-47452025-01-01391293210.4103/ijaai.ijaai_64_24Secondary hemophagocytic lymphohistiocytosis and isolated cerebellar ataxia due to disseminated tuberculosis with challenging management: A rare case reportRahul Kumar GuptaSammi PundirMansi KalaAvriti BavejaPranshul RawatAnuradha KhandelwalHemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder which occurs due to excessive immune response and high cytokine levels leading to tissue damage and organ failure. HLH can be primary and secondary. The etiology and presentation of secondary HLH remain diverse. Treatment of secondary HLH includes management of primary conditions and immunosuppressives. Several cases of secondary HLH due to tuberculosis (TB) have been reported in the past although their management beyond antitubercular therapy and follow-up was not reported. Here, we present a rare case report of secondary HLH and isolated cerebellar ataxia due to disseminated TB that responded to intravenous immunoglobulin in addition to antitubercular therapy and steroids. Patients showed complete response to therapy with normalization of hematological parameters and bone marrow findings. The patient was declared cured after 6 months of treatment.https://journals.lww.com/10.4103/ijaai.ijaai_64_24intravenous immunoglobulin in secondary hemophagocytic lymphohistiocytosisisolated cerebellar ataxia and secondary hemophagocytic lymphohistiocytosistuberculosis and hemophagocytic lymphohistiocytosis
spellingShingle Rahul Kumar Gupta
Sammi Pundir
Mansi Kala
Avriti Baveja
Pranshul Rawat
Anuradha Khandelwal
Secondary hemophagocytic lymphohistiocytosis and isolated cerebellar ataxia due to disseminated tuberculosis with challenging management: A rare case report
Indian Journal of Allergy Asthma and Immunology
intravenous immunoglobulin in secondary hemophagocytic lymphohistiocytosis
isolated cerebellar ataxia and secondary hemophagocytic lymphohistiocytosis
tuberculosis and hemophagocytic lymphohistiocytosis
title Secondary hemophagocytic lymphohistiocytosis and isolated cerebellar ataxia due to disseminated tuberculosis with challenging management: A rare case report
title_full Secondary hemophagocytic lymphohistiocytosis and isolated cerebellar ataxia due to disseminated tuberculosis with challenging management: A rare case report
title_fullStr Secondary hemophagocytic lymphohistiocytosis and isolated cerebellar ataxia due to disseminated tuberculosis with challenging management: A rare case report
title_full_unstemmed Secondary hemophagocytic lymphohistiocytosis and isolated cerebellar ataxia due to disseminated tuberculosis with challenging management: A rare case report
title_short Secondary hemophagocytic lymphohistiocytosis and isolated cerebellar ataxia due to disseminated tuberculosis with challenging management: A rare case report
title_sort secondary hemophagocytic lymphohistiocytosis and isolated cerebellar ataxia due to disseminated tuberculosis with challenging management a rare case report
topic intravenous immunoglobulin in secondary hemophagocytic lymphohistiocytosis
isolated cerebellar ataxia and secondary hemophagocytic lymphohistiocytosis
tuberculosis and hemophagocytic lymphohistiocytosis
url https://journals.lww.com/10.4103/ijaai.ijaai_64_24
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