Hemophagocytic syndrome triggered by intense physical activity and viral infection in a young adult female with three heterozygous mutations in Munc-18-2

Introduction. Hemophagocytic lymphohistiocytosis (HLH) is a rare, potentially life-threatening, hyperinflammatory syndrome caused by severe hypercytokinemia due to a highly stimulated, but ineffective immune response. Case report. We reported a 19-year-old woman presenting with fever, muscle and joi...

Popoln opis

Bibliografske podrobnosti

Principais autores:	Marković Olivera, Janić Dragana, Pavlović Milorad, Tukić Ljiljana, Janković Srđa, Filipović Branka, Marisavljević Dragomir
Format:	Artigo
Jezik:	Inglês
Izdano:	Ministry of Defence of the Republic of Serbia, University of Defence, Belgrade 2017-01-01
Serija:	Vojnosanitetski Pregled
Teme:	lymphohistocytosis, hemophagocytic inflammation immunologic factors physical exertion ebstein-barr virus mutation diagnosis, differential drug therapy
Online dostop:	http://www.doiserbia.nb.rs/img/doi/0042-8450/2017/0042-84501600224M.pdf
Oznake:	Označite Brez oznak, prvi označite!