Nalaganje...
Adult-onset Primary Hemophagocytic Lymphohistiocytosis: Reporting a Rare Case with Review of Literature
Hemophagocytic lymphohistiocytosis (HLH) is an uncommon, aggressive hematological syndrome. It is caused by an increased and unchecked proliferation of T lymphocytes and histiocytes. These cells secrete a large number of inflammatory cytokines and infiltrate various tissues causing multi-organ syste...
Shranjeno v:
| izdano v: | Cureus |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Cureus
2020
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7034735/ https://ncbi.nlm.nih.gov/pubmed/32133251 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.6723 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|