Deciphering the clinical profile and diagnostic framework of hemophagocytic lymphohistiocytosis in a tertiary care setting
Background: Hemophagocytic lymphohistiocytosis (HLH) is a severe hyperinflammatory disorder marked by intense yet ineffective immune activation, resulting in hemophagocytosis, systemic inflammation, and multi-organ dysfunction. The diagnosis has traditionally depended on the 2004 HLH criteria, while...
שמור ב:
| Principais autores: | , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Wolters Kluwer Medknow Publications
2024-12-01
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| סדרה: | MGM Journal of Medical Sciences |
| נושאים: | |
| גישה מקוונת: | https://doi.org/10.4103/mgmj.mgmj_321_24 |
| תגים: |
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
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