Department of Haematology, Aberdeen Royal Infirmary, NHS Grampian, Aberdeen, UK.
Department of Pathology, Aberdeen Royal Infirmary, NHS Grampian, Aberdeen, UK.
J R Coll Physicians Edinb. 2024 Mar;54(1):29-33. doi: 10.1177/14782715231220108. Epub 2023 Dec 30.
Haemophagocytic lymphohistiocytosis (HLH) is a rare, aggressive, excess immune activation syndrome. Diagnosis can be challenging due to its several clinical mimics including sepsis. There are multiple aetiologies of HLH; in adults, it is most commonly triggered by infection, malignancy, drugs and autoimmune processes. Failure to rapidly diagnose and treat this condition can be fatal. The management of HLH includes identifying and removing the trigger, supportive management and immunosuppression. Identifying the trigger is essential to inform the most appropriate type of immunosuppression. Here, we report a case of likely drug-induced HLH in a patient recently treated for hairy cell leukaemia. The culprit drug was thought to be co-trimoxazole and this case report highlights a very rare complication of this commonly used drug. We discuss our management approach with steroid monotherapy and withdrawal of co-trimoxazole.
噬血细胞性淋巴组织细胞增生症(HLH)是一种罕见的、侵袭性的、过度免疫激活综合征。由于其具有多种临床表现类似物,包括脓毒症,因此诊断具有一定挑战性。HLH 有多种病因;在成年人中,它最常由感染、恶性肿瘤、药物和自身免疫过程引发。如果不能迅速诊断和治疗这种疾病,可能会导致死亡。HLH 的治疗包括确定并去除诱因、支持性治疗和免疫抑制治疗。确定诱因对于告知最合适的免疫抑制类型至关重要。在这里,我们报告了一例最近接受治疗的毛细胞白血病患者可能由药物引起的 HLH。怀疑的罪魁祸首药物是复方磺胺甲噁唑,本病例报告强调了这种常用药物的一种非常罕见的并发症。我们讨论了我们的管理方法,即单独使用类固醇和停用复方磺胺甲噁唑。