Hemophagocytic Lymphohistiocytosis Associated with Respiratory Syncytial Virus Infection in an Immunocompetent Elderly Patient
Autor: | Arshpal Gill, Rubal Sharma, Ralph Kamel, Divya Asti, Yevgeniy Skaradinskiy |
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Rok vydání: | 2020 |
Předmět: |
Disseminated intravascular coagulation
Hemophagocytic lymphohistiocytosis business.industry Genetic heterogeneity Case Report General Medicine medicine.disease Malignancy Virus 03 medical and health sciences 0302 clinical medicine Immune system 030220 oncology & carcinogenesis Immunology Medicine Diseases of the blood and blood-forming organs Decompensation RC633-647.5 Respiratory system business 030215 immunology |
Zdroj: | Case Reports in Hematology, Vol 2020 (2020) Case Reports in Hematology |
ISSN: | 2090-6579 2090-6560 |
Popis: | Hemophagocytic lymphohistiocytosis is a serious and potentially fatal disorder characterized by excessive immune system activation. The disorder is diagnosed mainly based on laboratory, clinical, and pathologic criteria. The spectrum comprises hereditary or “primary” HLH that comprises genetically heterogeneous conditions, occurring during childhood. The secondary form presents later in life and is associated with several conditions mainly malignancy, autoimmune diseases, viral or bacterial infections, and hematological diseases. We present the case of an 80-year-old female patient who initially presented with an acute viral syndrome secondary to respiratory syncytial virus. The hospital course was complicated by disseminated intravascular coagulation and shock with multiorgan failure. Extensive workup revealed that several of the criteria for hemophagocytic lymphohistiocytosis were met. A review of literature fails to identify cases of hemophagocytic lymphohistiocytosis associated with respiratory syncytial virus in immunocompetent adults. This case report provides further insight on RSV as a possible etiologic agent associated with HLH and the importance of early recognition of this fatal disorder in RSV-positive patients who show unpredictable clinical decompensation. |
Databáze: | OpenAIRE |
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