| Literature DB >> 25114410 |
A M V R Narendra1, G Varun Kumar1, A Krishna Prasad1, M Shetty1, Megha S Uppin2, V R Srinivasan1.
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.Entities:
Keywords: HLH; NK cell dysfunction; PUO
Year: 2012 PMID: 25114410 PMCID: PMC4115081 DOI: 10.1007/s12288-012-0210-7
Source DB: PubMed Journal: Indian J Hematol Blood Transfus ISSN: 0971-4502 Impact factor: 0.900