Hemophagocytic lymphohistiocytosis and thrombotic microangiopathy after parvovirus B19 infection and renal transplantation: a case report

BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening disease characterized by hyperactivation of the immune system that causes hypercytokinemia and potentially multi organ failure. HLH can occur in patients with underlying rheumatic or autoinflammatory disorders. Addit...

Descripción completa

Detalles Bibliográficos
Autores principales: Steffen, C. J., Koch, N., Eckardt, K. U., Amann, K., Seelow, E., Schreiber, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506469/
https://www.ncbi.nlm.nih.gov/pubmed/34641801
http://dx.doi.org/10.1186/s12882-021-02538-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506469/
https://www.ncbi.nlm.nih.gov/pubmed/34641801
http://dx.doi.org/10.1186/s12882-021-02538-0

Ejemplares similares