| Literature DB >> 24783117 |
Sanjay A Natu1, Ujjwala S Keskar1, Manas K Behera2, Sambhaji C Chate3.
Abstract
Haemophagocytic lymphohistiocytosis (HLH) is a potentially fatal, hyper inflammatory condition which is caused by a highly stimulated but ineffective immune response. We are presenting here, a case of HLH which occurred in a 45 day infant. Presence of lung cavity and a lytic bone lesion in the skull, as was seen in this case, have not been reported in HLH in the literature. This raises a possibility of a simultaneous occurrence of HLH and Langerhans cell histiocytosis. In a child who presents with septicaemia but does not respond to treatment, the possibility of HLH needs to be considered.Entities:
Keywords: Familial haemophagocytic lymphohistiocytosis; Haemophagocytic lymphohistiocytosis; Lung cavity
Year: 2014 PMID: 24783117 PMCID: PMC4003621 DOI: 10.7860/JCDR/2014/6521.4145
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X