Publication: A case report of hemophagocytic lymphohistiocytosis (HLH) associated with sarcoidosis
Date
2024
Article Type
Case Report
Journal Title
Journal ISSN
ISSN 2822-1893 eISSN 2822-2016
Volume Title
Pages
Pages: 41 - 45
Publisher
Nepalese Respiratory Society
Abstract
Abstract:
Hemophagocytic Lymphohistiocytosis (HLH) is a rapidly progressing, fatal disorder characterized by severe systemic hyperinflammation presenting with unremitting fever, organomegaly (hepatosplenomegaly), cytopenias, raised inflammatory markers, liver failure, neurological issues, coagulopathy, and multiorgan failure. It is classified as primary due to mutations inherent to the individual causing increased macrophage activation or due to underlying secondary causes ranging from infections, malignancies, metabolic disorders, or rarely, rheumatological disorders such as juvenile idiopathic arthritis, SLE, sarcoidosis, and so on. However, the association between sarcoidosis and HLH has been rarely reported in the literature, which can present with features of sepsis, making the diagnosis challenging and requiring high clinical suspicion. We report the case of a patient with sarcoidosis presenting with recurrent fever, bilateral lower limb swelling, and fatigue, eventually developing fatal HLH that was unresponsive to high-dose steroids.
Description
Naresh Gurung
Department of Pulmonary, Critical Care, and Sleep Medicine, Nepal Mediciti Hospital
Ashish Karthak
Department of Pulmonary, Critical Care, and Sleep Medicine, Nepal Mediciti Hospital
Awin Saraf
Department of Cardiology, Nepal Mediciti Hospital
Sanjeet Krishna Shrestha
Department of Pulmonary, Critical Care, and Sleep Medicine, Nepal Mediciti Hospital
Keywords
Lymphohistiocytosis, hemophagocytic, sarcoidosis, pancytopenia, hyperinflammation
Identifier
https://doi.org/10.3126/nrj.v3i2.83173