Abstract
Hemophagocytic lymphohistiocytosis (HLH) is an immune disorder characterized by uncontrolled inflammation due to defective immune response. It may be familial or acquired, but both share a common feature of threatening the life of a patient and may lead to death unless treated by appropriate treatment. Here in we report a case of adult HLH. © 2012 Indian Society of Haematology & Transfusion Medicine.
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APA
Narendra, A. M. V. R., Varun Kumar, G., Krishna Prasad, A., Shetty, M., Uppin, M. S., & Srinivasan, V. R. (2014). Hemophagocytic lymphohistiocytosis. Indian Journal of Hematology and Blood Transfusion, 30(3), 204–207. https://doi.org/10.1007/s12288-012-0210-7
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