Hemophagocytic Lymphohistiocytosis Secondary to Adult-Onset Still’s Disease

Hemophagocytic lymphohistiocytosis (HLH) is a rare hematological condition resulting from dysregulation of the immune system. This unusual clinical syndrome is characterized by fever, cytopenia, liver dysfunction, increased ferritin level, and evidence of hemophagocytosis in the bone marrow. We repo...

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Detalles Bibliográficos
Autores principales: Barman, Bhupen, Jamil, Md, Kalita, Pranjal, Dey, Biswajit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520583/
https://www.ncbi.nlm.nih.gov/pubmed/34671525
http://dx.doi.org/10.7759/cureus.18037

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520583/
https://www.ncbi.nlm.nih.gov/pubmed/34671525
http://dx.doi.org/10.7759/cureus.18037

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