An Unusual Presentation of Adult-Onset Still’s Disease as Hemophagocytic Lymphohistiocytosis in a Male Patient

Hemophagocytic lymphohistiocytosis (HLH) is an aggressive and potentially fatal condition characterized by immune activation and multi-organ dysfunction. HLH can be inherited in an autosomal recessive fashion, but can also be secondary to infections, malignancy, immunosuppression, and autoimmune con...

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Detalles Bibliográficos
Autores principales: Kuruvilla, Neenu, Rajendran, Rahul, Thomas, Shilpa S, Ali KM, Irshad, Kurian, Sheela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682946/
https://www.ncbi.nlm.nih.gov/pubmed/33240728
http://dx.doi.org/10.7759/cureus.11139

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682946/
https://www.ncbi.nlm.nih.gov/pubmed/33240728
http://dx.doi.org/10.7759/cureus.11139

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