Hemophagocytic lymphohistiocytosis in a patient with Sjögren’s syndrome: case report and review

Hemophagocytic lymphohistiocytosis (HLH) is a very rare syndrome with a mortality up to 95% of cases if not treated. It is characterised by an excessive activation of the immune system that leads to a disproportionate and destructive inflammatory response. The high mortality rates are in part due to...

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Detalles Bibliográficos
Autores principales: García-Montoya, L., Sáenz-Tenorio, C. N., Janta, I., Menárguez, J., López-Longo, F. J., Monteagudo, I., Naredo, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Cases with a Message
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102319/
https://www.ncbi.nlm.nih.gov/pubmed/27853859
http://dx.doi.org/10.1007/s00296-016-3601-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102319/
https://www.ncbi.nlm.nih.gov/pubmed/27853859
http://dx.doi.org/10.1007/s00296-016-3601-5

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