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The Dilemma of Diagnosing Hemophagocytic Lymphohistiocytosis in Sickle Cell Disease
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder due to uncontrolled activation of macrophage and cytokine release, which can be due to either genetic causes (familial) or secondary to infections malignancy and other less common cause. Parvovirus B19 rarely causes HLH. Diagnos...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831292/ https://www.ncbi.nlm.nih.gov/pubmed/33510976 http://dx.doi.org/10.7759/cureus.12255 |