Mechi Ahmed Mohamad, Al-Khalidi Alhan Abbas, Hasan Thulfiqar Azeez
Internal Medicine Department, College of Medicine University of Kufa Najaf Iraq.
Internal Medicine Department, College of Medicine Jabir Ibn Hayyan Medical University Najaf Iraq.
Clin Case Rep. 2023 Mar 20;11(3):e7096. doi: 10.1002/ccr3.7096. eCollection 2023 Mar.
Hemophagocytic Lymphohistiocytosis syndrome is fatal hyper-inflammatory condition due to over-activation of the immune system, being of primary and secondary types. This case report emphasizes the difficulty and challenge in and of the HLH diagnosis, and therapy should be employed promptly given the high mortality associated with HLH.
噬血细胞性淋巴组织细胞增生症综合征是一种由于免疫系统过度激活导致的致命性高炎症状态,分为原发性和继发性两种类型。本病例报告强调了HLH诊断的困难和挑战,鉴于HLH相关的高死亡率,应及时进行治疗。