Publication: Familial Hemophagocytic Lymphohistiocytosis (FHL), Report of two Unique Cases
Date
2015
Journal Title
Journal ISSN
Volume Title
Publisher
Nepal Paediatric Society (JNPS)
Abstract
Abstract:
Familial hemophagocytic lymphohistiocytosis (FHLH) is a rare genetic disorder associated with early onset in life with overwhelming activation of T lymphocytes and macrophages invariably leading to death. We present two cases of FHLH admitted to our hospital at different points of time. First child presented with multiple episodes of GTCS and high grade fever. There was a history of sibling death before. He was having hepatosplenomegaly with leucopenia, hyper-triglyceridemia, hyper-ferritinemia and bone marrow revealed abundant hemophagocytes in smear. Second case was a 6 month male with complaint of (Generalised Tonic Clonic Seizure (GTCS) with past history of repeated attacks of acute Respiratory Infection and neuroinfection. Previous sibling died in similar presentation. He was having hepatosplenomegaly, leucopenia, hyper triglyceridemia, hyper ferritinemia with abundant hemophagocytes in bone marrow smear. Both the cases were diagnosed as FHLH and treated according to protocol.
Description
Shubhankar Mishra
MKCG Medical College, Berhampur, Odhisa
Sunil Kumar Agarwalla
MKCG Medical College, Berhampur, Odhisa
Sushree Smita Behura
MKCG Medical College, Berhampur, Odhisa
Gouranga Charan Pattnaik
MKCG Medical College, Berhampur, Odhisa
Keywords
Histiocytosis, Hemophagocytes, Pancytopenia, Stem cell