Secondary haemophagocytic lymphohistiocytosis: Experience from the Uppsala University Hospital

Background. Haemophagocytic lymphohistiocytosis (HLH) is a rare clinical syndrome characterized by fever, hepatosplenomegaly, cytopenia, and progressive multiple-organ failure. HLH in adults is often secondary to autoimmune diseases, cancer, or infections in contrast to familial HLH. Treatment of se...

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Detalles Bibliográficos
Autor principal: Karlsson, Torbjörn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa Healthcare 2015
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816886/
https://www.ncbi.nlm.nih.gov/pubmed/26212358
http://dx.doi.org/10.3109/03009734.2015.1064500

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816886/
https://www.ncbi.nlm.nih.gov/pubmed/26212358
http://dx.doi.org/10.3109/03009734.2015.1064500

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