Cytomegalovirus-Induced Hemophagocytic Lymphohistiocytosis in an Immunocompromised Patient with Inflammatory Bowel Disease
Hemophagocytic lymphohistiocytosis (HLH) is a rare and often fatal syndrome of immune hyperactivation, cytokine dysregulation, and severe inflammation. This severe syndrome is commonly triggered by infection, malignancy, autoimmunity, or immunosuppression. We present herein the case of a 56-year-old...
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Format: | Article |
Language: | English |
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Hindawi Limited
2024-01-01
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Series: | Case Reports in Hematology |
Online Access: | http://dx.doi.org/10.1155/2024/6964818 |
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author | Alessandro Pedicelli René P. Michel Nick Krassakopoulos |
author_facet | Alessandro Pedicelli René P. Michel Nick Krassakopoulos |
author_sort | Alessandro Pedicelli |
collection | DOAJ |
description | Hemophagocytic lymphohistiocytosis (HLH) is a rare and often fatal syndrome of immune hyperactivation, cytokine dysregulation, and severe inflammation. This severe syndrome is commonly triggered by infection, malignancy, autoimmunity, or immunosuppression. We present herein the case of a 56-year-old-female diagnosed with HLH triggered by an acute cytomegalovirus (CMV) infection with viremia in the context of immunosuppression for inflammatory bowel disease. This case highlights the importance of utilizing multiple diagnostic tools, prompt initiation of anti-hemophagocytic treatment, and management of the underlying etiology, to prevent significant morbidity and mortality. |
first_indexed | 2024-04-24T11:42:09Z |
format | Article |
id | doaj.art-ef7348f4eb0840ce90ea669a1bf10fbf |
institution | Directory Open Access Journal |
issn | 2090-6579 |
language | English |
last_indexed | 2024-04-24T11:42:09Z |
publishDate | 2024-01-01 |
publisher | Hindawi Limited |
record_format | Article |
series | Case Reports in Hematology |
spelling | doaj.art-ef7348f4eb0840ce90ea669a1bf10fbf2024-04-10T00:00:04ZengHindawi LimitedCase Reports in Hematology2090-65792024-01-01202410.1155/2024/6964818Cytomegalovirus-Induced Hemophagocytic Lymphohistiocytosis in an Immunocompromised Patient with Inflammatory Bowel DiseaseAlessandro Pedicelli0René P. Michel1Nick Krassakopoulos2Division of Internal MedicineDepartment of PathologyDivision of Internal MedicineHemophagocytic lymphohistiocytosis (HLH) is a rare and often fatal syndrome of immune hyperactivation, cytokine dysregulation, and severe inflammation. This severe syndrome is commonly triggered by infection, malignancy, autoimmunity, or immunosuppression. We present herein the case of a 56-year-old-female diagnosed with HLH triggered by an acute cytomegalovirus (CMV) infection with viremia in the context of immunosuppression for inflammatory bowel disease. This case highlights the importance of utilizing multiple diagnostic tools, prompt initiation of anti-hemophagocytic treatment, and management of the underlying etiology, to prevent significant morbidity and mortality.http://dx.doi.org/10.1155/2024/6964818 |
spellingShingle | Alessandro Pedicelli René P. Michel Nick Krassakopoulos Cytomegalovirus-Induced Hemophagocytic Lymphohistiocytosis in an Immunocompromised Patient with Inflammatory Bowel Disease Case Reports in Hematology |
title | Cytomegalovirus-Induced Hemophagocytic Lymphohistiocytosis in an Immunocompromised Patient with Inflammatory Bowel Disease |
title_full | Cytomegalovirus-Induced Hemophagocytic Lymphohistiocytosis in an Immunocompromised Patient with Inflammatory Bowel Disease |
title_fullStr | Cytomegalovirus-Induced Hemophagocytic Lymphohistiocytosis in an Immunocompromised Patient with Inflammatory Bowel Disease |
title_full_unstemmed | Cytomegalovirus-Induced Hemophagocytic Lymphohistiocytosis in an Immunocompromised Patient with Inflammatory Bowel Disease |
title_short | Cytomegalovirus-Induced Hemophagocytic Lymphohistiocytosis in an Immunocompromised Patient with Inflammatory Bowel Disease |
title_sort | cytomegalovirus induced hemophagocytic lymphohistiocytosis in an immunocompromised patient with inflammatory bowel disease |
url | http://dx.doi.org/10.1155/2024/6964818 |
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