Prasad Supritha, Mushfiq Farooqui Iman, AlZoubi Lujain, Arami Shiva
Internal Medicine, University of Illinois at Chicago, Chicago, USA.
Medicine, Aga Khan University, Karachi, PAK.
Cureus. 2023 Jul 12;15(7):e41780. doi: 10.7759/cureus.41780. eCollection 2023 Jul.
T-cell large granular lymphocytic (LGL) leukemia is characterized by a clonal proliferation of CD3+ T-cells and has been associated with rheumatoid arthritis (RA). Splenomegaly is a common finding and a majority of cases present with cytopenia. Felty syndrome (FS) is characterized by neutropenia and splenomegaly and is also classically described in the literature for its association with RA. Similarities in clinical features, pathogenesis, management, genetics, and immunologic basis of FS and T-cell LGL leukemia have led to the suggestion that they exist on the same spectrum of disease. We present a case of T-cell LGL leukemia in an RA patient with clinical features not distinguishable from features of FS.
T细胞大颗粒淋巴细胞(LGL)白血病的特征是CD3+T细胞的克隆性增殖,并且与类风湿性关节炎(RA)有关。脾肿大是常见表现,大多数病例伴有血细胞减少。费尔蒂综合征(FS)的特征是中性粒细胞减少和脾肿大,在文献中也经典地描述了其与RA的关联。FS和T细胞LGL白血病在临床特征、发病机制、治疗、遗传学和免疫基础方面的相似性,导致有人提出它们存在于同一疾病谱中。我们报告一例RA患者的T细胞LGL白血病病例,其临床特征与FS的特征无法区分。