A case of T-cell large granular lymphocytic leukemia with autoimmune hemolytic anemia and literature review.

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL American journal of translational research Pub Date : 2024-10-15 eCollection Date: 2024-01-01 DOI:10.62347/URFI7647
Shu-Yu Wang, Yan Li
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Abstract

T-cell large granular lymphocyte leukemia (T-LGLL), which is associated with autoimmune diseases, has been described. However, T-LGLL with B-cell dyscrasias presenting as autoimmune hemolytic anemia has been less frequently reported. Here, we report a rare case of combined papillary thyroid cancer (PTC), discuss the possible relationship between autoimmune hemolytic anemia (AIHA) and TLGLL, and review the literature. The patient presented with pancytopenia and systemic jaundice. Fortunately, the patient responded well to hormone and immunosuppressive (methotrexate) therapy. However, this insight is based on one rare case, and the pathogenesis of this disease requires further clinical research for clarification.

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一例 T 细胞大颗粒淋巴细胞白血病合并自身免疫性溶血性贫血及文献综述。
与自身免疫性疾病相关的 T 细胞大颗粒淋巴细胞白血病(T-LGLL)已有报道。然而,T-LGLL伴有B细胞异常,表现为自身免疫性溶血性贫血的病例却鲜有报道。在此,我们报告了一例罕见的合并甲状腺乳头状癌(PTC)的病例,讨论了自身免疫性溶血性贫血(AIHA)与 TLGLL 之间可能存在的关系,并回顾了相关文献。患者出现全血细胞减少和全身性黄疸。幸运的是,患者对激素和免疫抑制剂(甲氨蝶呤)治疗反应良好。然而,这一见解只是基于一个罕见病例,该病的发病机制还需要进一步的临床研究才能明确。
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American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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