The great masquerader: Hemophagocytic lymphohistiocytosis secondary to cytomegalovirus infection in an immunocompetent young man

Hemophagocytic lymphohistiocytosis (HLH) is a rare, poorly recognized and underdiagnosed syndrome of excessive immune activation, which is rapidly fatal. HLH can occur as a familial or secondary disorder. Secondary HLH is most commonly associated with infections, malignancies, or autoimmune diseases...

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Detalles Bibliográficos
Autores principales: Singh, Akanksha, Chauhan, Ajay, Padole, Vaibhav, Chhabra, Devyani, Upneja, Raghav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567245/
https://www.ncbi.nlm.nih.gov/pubmed/33102367
http://dx.doi.org/10.4103/jfmpc.jfmpc_274_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567245/
https://www.ncbi.nlm.nih.gov/pubmed/33102367
http://dx.doi.org/10.4103/jfmpc.jfmpc_274_20

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