Hemophagocytic lymphohistiocytosis complicated by polyserositis: A case report

BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a rare group of disorders of immune dysregulation characterized by clinical symptoms of severe inflammation. There are basically two types of clinical scenarios: Familial HLH and sporadic HLH. It is thought that the syndrome is implicated in th...

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Detalles Bibliográficos
Autores principales: Zhu, Ping, Ye, Qing, Li, Ting-Hong, Han, Tao, Wang, Feng-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795728/
https://www.ncbi.nlm.nih.gov/pubmed/31624756
http://dx.doi.org/10.12998/wjcc.v7.i19.3069

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795728/
https://www.ncbi.nlm.nih.gov/pubmed/31624756
http://dx.doi.org/10.12998/wjcc.v7.i19.3069

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