Muñoz Agustín M, Orozco Niño José A, Seehaus Cristian M, Giménez Conca Alberto D, Chuliber Fernando A, Lo Giudice Luciano F, Bendek Georgina E
Servicio de Clínica Médica, Hospital Italiano de Buenos Aires, Argentina. E-mail:
Servicio de Clínica Médica, Hospital Italiano de Buenos Aires, Argentina.
Medicina (B Aires). 2021;81(6):1060-1064.
Large granular T-cell leukemia is a rare cytotoxic lymphocyte disorder. These cells play an integral role in the immune system and are divided into 2 lineages: CD3 T positive and natural killer. Its proliferation and uncontrolled cytotoxicity can generate autoimmunity or malignancy. Rheumatoid arthritis is the most common autoimmune disease in individuals with this type of leukemia, however, it has been associated with a wide spectrum of other autoimmune diseases and hematological conditions including hemolytic anemia, pure red blood cell aplasia, and neutropenia, leading to recurring bacterial infections. The following is a case of a 72-year-old female with a history of large granular T-cell leukemia and manifestations compatible with rheumatoid arthritis, which occurs with a severe Evans syndrome with a good initial and sustained response to gamma globulin, corticosteroid therapy, and rituximab.
大颗粒T细胞白血病是一种罕见的细胞毒性淋巴细胞疾病。这些细胞在免疫系统中发挥着不可或缺的作用,可分为两个谱系:CD3 T阳性和自然杀伤细胞。其增殖和不受控制的细胞毒性可导致自身免疫或恶性肿瘤。类风湿性关节炎是患有这种白血病的个体中最常见的自身免疫性疾病,然而,它还与多种其他自身免疫性疾病和血液系统疾病有关,包括溶血性贫血、纯红细胞再生障碍和中性粒细胞减少症,可导致反复的细菌感染。以下是一名72岁女性的病例,她有大颗粒T细胞白血病病史,表现与类风湿性关节炎相符,同时伴有严重的伊文斯综合征,对γ球蛋白、皮质类固醇治疗和利妥昔单抗有良好的初始和持续反应。