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An Unusual Presentation of Systemic Lupus Erythematosus as Hemophagocytic Lymphohistiocytosis in a Male.
Hemophagocytic lymphohistiocytosis (HLH) is an aggressive and life-threatening hyper-inflammatory condition characterized by excessive activation of macrophages and T cells resulting in multi-organ dysfunction. HLH can be primary/familial or secondary to infections, malignancy, immunosuppression, an...
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| Vydáno v: | Cureus |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Cureus
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6701905/ https://ncbi.nlm.nih.gov/pubmed/31482047 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.5427 |
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