Gorodetskiy Vadim, Probatova Natalya, Sidorova Yulia, Kupryshina Natalia, Obukhova Tatiana, Vasilyev Vladimir, Ryzhikova Natalya, Sudarikov Andrey
Department of Intensive Methods of Therapy, V. A. Nasonova Research Institute of Rheumatology Moscow, Russia.
Department of Pathology, N.N. Blokhin Russian Cancer Research Center Moscow, Russia.
Am J Blood Res. 2021 Jun 15;11(3):227-237. eCollection 2021.
T cell large granular lymphocytic (T-LGL) leukemia is a rare type of mature T cell neoplasm. The typical features of T-LGL leukemia include an increased number of large granular lymphocytes in the peripheral blood, cytopenia (most commonly neutropenia), and mild-to-moderate splenomegaly. Up to 28% of patients with T-LGL leukemia have rheumatoid arthritis (RA). This study reports ten atypical cases (seven women and three men, median age 60.5 years) of RA-associated T-LGL leukemia presenting with lymphopenia, severe neutropenia, and marked splenomegaly. The weight of the spleens ranged from 892 to 2100 g (median 1100 g). Bone marrow histology and differential counts of bone marrow aspirates revealed no peculiarities in nine of ten cases. The red pulp of the spleen was expanded and showed moderate to strong infiltration by medium-sized slightly pleomorphic lymphocytes in nine cases and subtle infiltration in one. Although lymphocytic infiltration involved both cords and sinusoids, it was more apparent within the splenic cords. The white pulp was preserved and contained prominent germinal centers in eight patients and was atrophic in two patients. Immunohistochemically, malignant lymphocytes were CD3+, CD43+, and CD4- in all cases and TIA-1+ in nine out of ten. TCRαβ positivity and TCRγδ positivity was observed in six and four cases out of ten, respectively. All ten patients had T cell clonality in the spleen tissue, but in three cases it was absent in both blood and bone marrow. STAT3 mutations in the spleen tissue were detected in three of ten cases. In all eight cases studied, neither isochromosome 7q nor trisomy 8 was detected in the spleen tissue. Cases of RA-associated T-LGL leukemia with low LGL count in the peripheral blood, neutropenia, and marked splenomegaly present a diagnostic challenge and can be misdiagnosed as Felty's syndrome or hepatosplenic T cell lymphoma.
T细胞大颗粒淋巴细胞(T-LGL)白血病是一种罕见的成熟T细胞肿瘤。T-LGL白血病的典型特征包括外周血中大颗粒淋巴细胞数量增加、血细胞减少(最常见的是中性粒细胞减少)以及轻至中度脾肿大。高达28%的T-LGL白血病患者患有类风湿性关节炎(RA)。本研究报告了10例非典型的RA相关T-LGL白血病病例(7名女性和3名男性,中位年龄60.5岁),这些病例表现为淋巴细胞减少、严重中性粒细胞减少和明显脾肿大。脾脏重量范围为892至2100克(中位值1100克)。10例中有9例骨髓组织学检查和骨髓穿刺涂片分类计数未见异常。9例脾脏红髓扩大,可见中等大小、轻度多形性淋巴细胞中度至重度浸润,1例为轻微浸润。虽然淋巴细胞浸润累及脾索和脾窦,但在脾索内更明显。白髓保存,8例患者有明显的生发中心,2例萎缩。免疫组化显示,所有病例中恶性淋巴细胞均为CD3+、CD43+、CD4-,10例中有9例为TIA-1+。10例中有6例和4例分别观察到TCRαβ阳性和TCRγδ阳性。所有10例患者脾脏组织均有T细胞克隆性,但3例血液和骨髓中均无。10例中有3例在脾脏组织中检测到STAT3突变。在所有8例研究病例中,脾脏组织均未检测到7号染色体等臂染色体或8号染色体三体。外周血LGL计数低、中性粒细胞减少和明显脾肿大的RA相关T-LGL白血病病例诊断具有挑战性,可能被误诊为费尔蒂综合征或肝脾T细胞淋巴瘤。