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Severe COVID-19-Induced Hemophagocytic Lymphohistiocytosis
Shahkar Khan1, Taqi A Rizvi1, Waleed Sadiq2
1Internal Medicine, Staten Island University Hospital, New York City, USA.
Insights
A severe case of coronavirus disease 2019 (COVID-19) may trigger secondary hemophagocytic lymphohistiocytosis (HLH), a rare and fatal condition. This case highlights the critical need for early recognition and management of HLH in COVID-19 patients.
Area of Science:
- Infectious Diseases
- Hematology
- Critical Care Medicine
Background:
- Secondary hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening hyperinflammatory syndrome.
- Coronavirus disease 2019 (COVID-19) has been associated with various hyperinflammatory complications.
- The potential link between severe COVID-19 and secondary HLH requires further investigation.
Abstract:
We reported a case of secondary hemophagocytic lymphohistiocytosis (HLH), a rare and life-threatening condition, which was suspected to have been triggered by a severe case of coronavirus disease 2019 (COVID-19). A 50-year-old man with a past medical history of ulcerative colitis with recent pancolitis status post colectomy and ileostomy two weeks before presentation presented to the emergency department with one week of subjective fevers, weakness, watery diarrhea, and decreased oral intake. A CT scan showed fluid in the rectum and post-surgical changes from his recent colectomy along with diffuse reticulonodular opacities of the lungs. His COVID-19 reverse transcriptase-polymerase chain reaction (RT-PCR) test was positive. Over the subsequent days, the patient's condition worsened as he developed worsening acute hypoxic respiratory failure with diffuse lymphadenopathy, splenomegaly, worsening cytopenias, and increased ferritin of >100,000 ng/ml on hospital day six. Hematology oncology was consulted and he was started on empiric steroid therapy followed by etoposide. However, his condition continued to worsen, and eventually, the patient passed away on hospital day eight.
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