Atas Unal, Cerci Kubra, Tuncer Sema, Karakus Volkan
Department of Hematology, Antalya Training and Research Hospital, Antalya, Turkiye.
Department of Internal Medicine, Antalya Training and Research Hospital, Antalya, Turkiye.
North Clin Istanb. 2024 Oct 3;11(5):488-491. doi: 10.14744/nci.2022.66742. eCollection 2024.
Evans syndrome (ES) is a spectrum of diseases in which the combination of autoimmune hemolytic anemia and immune thrombocytopenia or sometimes neutropenia. ES has been accepted usually as an idiopathic condition, but it may be secondary. The coexistence of autoimmune cytopenias and Hodgkin lymphoma (HL) is rarely observed and the rate of ES in HL patients is not clear. Here we describe a 56-year-old male patient who presented with ES and was diagnosed with HL. After corticosteroids, intravenous immunoglobulin (IVIG) and ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine) treatment, immune cytopenias were completely resolved. The literature is also reviewed and we found 16 cases in which HL and ES coexist. Although AIHA and immune thrombocytopenia usually develop simultaneously, they rarely occur at different times. Many aspects of the pathogenesis are unknown, but it is thought to be a complex immunological background. Corticosteroids and/or IVIG are the most commonly used first-choice drugs in the initial treatment of ES. Response rates to treatment are variable and response to treatment may be poor, particularly with underlying conditions. If detected, the underlying lymphoma should be treated.
伊文氏综合征(ES)是一系列疾病,其特征为自身免疫性溶血性贫血与免疫性血小板减少症合并存在,有时还伴有中性粒细胞减少症。ES通常被认为是一种特发性疾病,但也可能是继发性的。自身免疫性血细胞减少症与霍奇金淋巴瘤(HL)并存的情况很少见,HL患者中ES的发生率尚不清楚。在此,我们描述了一名56岁男性患者,他表现为ES并被诊断为HL。经过皮质类固醇、静脉注射免疫球蛋白(IVIG)和ABVD(阿霉素、博来霉素、长春花碱、达卡巴嗪)治疗后,免疫性血细胞减少症完全缓解。我们还对文献进行了综述,发现了16例HL与ES并存的病例。虽然自身免疫性溶血性贫血(AIHA)和免疫性血小板减少症通常同时发生,但它们很少在不同时间出现。发病机制的许多方面尚不清楚,但被认为具有复杂的免疫背景。皮质类固醇和/或IVIG是ES初始治疗中最常用的首选药物。治疗反应率各不相同,对治疗的反应可能较差,尤其是在存在基础疾病的情况下。如果检测到潜在的淋巴瘤,应进行治疗。