Systemic autoimmune abnormalities complicated by cytomegalovirus-induced hemophagocytic lymphohistiocytosis: A case report

BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a rare but life-threatening disorder, characterized by a hyperimmune response. The mortality is high despite progress being made in the diagnosis and treatment of the disease. HLH is traditionally divided into primary (familial or genetic) and...

Descripción completa

Detalles Bibliográficos
Autores principales: Miao, Shu-Xian, Wu, Zhi-Qi, Xu, Hua-Guo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642531/
https://www.ncbi.nlm.nih.gov/pubmed/33195665
http://dx.doi.org/10.12998/wjcc.v8.i20.4946

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642531/
https://www.ncbi.nlm.nih.gov/pubmed/33195665
http://dx.doi.org/10.12998/wjcc.v8.i20.4946

Ejemplares similares