Načítá se...
Hemophagocytic Lymphohistiocytosis Complicating Systemic Sarcoidosis
Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening hyperinflammatory syndrome characterized by histiocyte proliferation and hemophagocytosis. Primary HLH is caused by genetic defects, whereas secondary HLH occurs in the setting of underlying diseases, such as infections, malignanci...
Uloženo v:
| Vydáno v: | Cureus |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Cureus
2018
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6101461/ https://ncbi.nlm.nih.gov/pubmed/30131931 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.2838 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|