在类风湿关节炎- Felty综合征和肝脾T细胞淋巴瘤面罩的情况下,非白血病T细胞大颗粒淋巴细胞白血病变异伴明显脾肿大和中性粒细胞减少。

American journal of blood research Pub Date : 2021-06-15 eCollection Date: 2021-01-01
Vadim Gorodetskiy, Natalya Probatova, Yulia Sidorova, Natalia Kupryshina, Tatiana Obukhova, Vladimir Vasilyev, Natalya Ryzhikova, Andrey Sudarikov
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引用次数: 0

摘要

T细胞大颗粒淋巴细胞白血病(T- lgl)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、细胞减少(最常见的是中性粒细胞减少)和轻度至中度脾肿大。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ra相关T-LGL白血病的非典型病例(7女3男,中位年龄60.5岁),表现为淋巴细胞减少、严重中性粒细胞减少和明显的脾肿大。脾脏重量为892 ~ 2100 g(中位数为1100 g)。10例患者中有9例骨髓组织学和骨髓吸出物的鉴别计数未见异常。脾红髓肿大,9例呈中至强浸润,有中型微多形性淋巴细胞浸润,1例呈微浸润。虽然淋巴细胞浸润累及脾索和窦状窦,但在脾索内更为明显。白色髓质保存完好,8例患者有突出的生发中心,2例患者萎缩。免疫组化结果显示,恶性淋巴细胞均为CD3+、CD43+和CD4-, 10例中有9例为TIA-1+。TCRαβ阳性6例,TCRγδ阳性4例。所有10名患者的脾脏组织中都有T细胞克隆,但有3名患者的血液和骨髓中都没有T细胞克隆。10例中有3例在脾脏组织中检测到STAT3突变。在研究的所有8例病例中,脾脏组织中均未检测到7q同工染色体和8三体。ra相关T-LGL白血病伴外周血LGL计数低、中性粒细胞减少和明显脾肿大的病例存在诊断挑战,可能误诊为Felty综合征或肝脾T细胞淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The non-leukemic T cell large granular lymphocytic leukemia variant with marked splenomegaly and neutropenia in the setting of rheumatoid arthritis - Felty syndrome and hepatosplenic T cell lymphoma mask.

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.

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American journal of blood research
American journal of blood research MEDICINE, RESEARCH & EXPERIMENTAL-
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