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T cell large granular lymphocytic leukemia in association with Sjogren's syndrome.

机译:T细胞大颗粒性淋巴细胞白血病与干燥综合征。

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摘要

T cell large granular lymphocytic (LGL) leukemia is a rare condition accounting for 2-3% of all mature lymphoid leukemias. Here, we present the case of a 73-year-old woman presenting with neutropenia and anemia (hemoglobin 9.9 g/dl). Hematological assessment revealed the presence of a T cell LGL leukemia. At the time of T cell LGL leukemia diagnosis, the patient developed xerophthalmia and xerostomia, and a diagnosis of Sjogren's syndrome was made following salivary gland biopsy. The finding of large granular lymphocytes in the context of autoimmune disorders is well-known, though it often occurs with rheumatoid arthritis or in association with a positive autoantibody titer in the absence of an overt clinical picture. The concomitant presentation of T cell LGL leukemia with Sjogren's syndrome is a rare event which is worth reporting. Our patient was managed with immunosuppressive therapy and is still alive.
机译:T细胞大颗粒淋巴细胞白血病(LGL)是一种罕见病,占所有成熟淋巴白血病的2-3%。在此,我们介绍了一名73岁女性出现中性粒细胞减少和贫血(血红蛋白9.9 g / dl)的情况。血液学评估显示存在T细胞LGL白血病。在诊断T细胞LGL白血病时,患者出现了干眼症和口干症,并在唾液腺活检后做出了干燥综合征的诊断。在自身免疫性疾病中发现大颗粒淋巴细胞是众所周知的,尽管它通常与类风湿性关节炎一起发生,或者在没有明显临床表现的情况下与阳性自身抗体滴度有关。 T细胞LGL白血病与干燥综合征的同时出现是罕见的事件,值得报告。我们的患者接受了免疫抑制疗法的治疗,现在还活着。

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