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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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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Informa Healthcare
2015
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| 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 |