Joncas J H, Russo P, Brochu P, Simard P, Brisebois J, Dubé J, Marton D, Leclerc J M, Hume H, Rivard G E
Department of Microbiology, Hôpital Sainte-Justine, Montreal, Quebec, Canada.
J Clin Oncol. 1990 Mar;8(3):378-84. doi: 10.1200/JCO.1990.8.3.378.
Polymorphic B-cell lymphoma seen in four patients with congenital immunodeficiencies and in two patients with leukemia receiving chemotherapy was associated with the Epstein-Barr virus (EBV). The tumors had characteristic histologic features: they were polymorphic consisting of a mixture of lymphoblasts and differentiated cells including plasma cells, and areas of hemorrhagic necrosis were prominent. The tumors were either polyclonal, monoclonal, or multiclonal. Patients with congenital immunodeficiencies who developed these tumors died despite radiotherapy, corticosteroids plus acyclovir, or a combination of intravenous (IV) immunoglobulins and alpha 2 interferon. Patients with leukemia recovered when immunosuppressive drugs were discontinued and leukemia has not recurred over a period of 2 and 4 years, respectively, in the two patients.
在4例先天性免疫缺陷患者和2例接受化疗的白血病患者中发现的多形性B细胞淋巴瘤与爱泼斯坦-巴尔病毒(EBV)有关。这些肿瘤具有特征性的组织学特征:它们是多形性的,由淋巴母细胞和包括浆细胞在内的分化细胞混合组成,出血坏死区域很明显。肿瘤要么是多克隆性的、单克隆性的,要么是多克隆性的。发生这些肿瘤的先天性免疫缺陷患者尽管接受了放疗、皮质类固醇加阿昔洛韦,或静脉注射(IV)免疫球蛋白和α2干扰素联合治疗,但仍死亡。白血病患者在停用免疫抑制药物后康复,在这两名患者中,白血病分别在2年和4年期间未复发。