Journal of Cardiovascular Disease Research
Identification and classification of hemophagocytic lymphohistiocytosis: clinical, laboratory, and prognostic insights from bone marrow aspiration analysis
Swetha Kesarapu, Pramod Kumar Pamu, Dr. Tara Roshni Paul, Dr. Sree Bhushan Raju, YSN Raju, Dr. Sadashivuudu Gundanti
JCDR. 2024: 3964 -3971
Abstract
Background: Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening disorder characterized by excessive activation of the immune system, leading to uncontrolled proliferation of histiocytes and T cells. This study aims to identify and classify cases of hemophagocytosis observed in bone marrow aspiration samples and to provide clinical, laboratory, and prognostic insights.
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