Wu Qingqing, Yu Yixiu, Feng Shenhong, Fang Bingqian, Zheng Renzhi, Sun Weidong, Zhao Jianzhi
Department of Hematology, Shaoxing Central Hospital, The Central Hospital of Shaoxing University, Shaoxing 312030, China.
IDCases. 2024 Apr 15;36:e01954. doi: 10.1016/j.idcr.2024.e01954. eCollection 2024.
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disease characterized by a hyperinflammatory syndrome and impairment of multiple organ systems. Talaromycosis marneffei (TSM) is an opportunistic infection mostly found in immunosuppressed populations, such as those with acquired immunodeficiency syndrome (AIDS), and is prevalent in southern China. However, HLH secondary to TSM is extremely rare and has only been reported in isolated cases. A 30-year-old patient with recurrent high fever and progressive cytopenia was diagnosed with HLH secondary to disseminated TSM with AIDS and -thalassemia. The patient remained in sustained remission without recurrence after effective treatment with antifungals and glucocorticoids.
噬血细胞性淋巴组织细胞增生症(HLH)是一种危及生命的疾病,其特征为高炎症综合征和多器官系统损害。马尔尼菲篮状菌病(TSM)是一种机会性感染,多见于免疫抑制人群,如获得性免疫缺陷综合征(AIDS)患者,在中国南方地区较为流行。然而,TSM继发的HLH极为罕见,仅在个别病例中有报道。一名30岁反复高热和进行性血细胞减少的患者被诊断为播散性TSM合并AIDS和β地中海贫血继发的HLH。经抗真菌药和糖皮质激素有效治疗后,患者持续缓解且未复发。