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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...
Autores principales: | Kuruvilla, Neenu, Rajendran, Rahul, Thomas, Shilpa S, Ali KM, Irshad, Kurian, Sheela |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2020
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Materias: | |
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 |
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