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

被引:0
作者
Wang, Shu-Yu [1 ,2 ]
Li, Yan [2 ]
机构
[1] Hebei North Univ, Dept Grad Sch, Zhangjiakou 075000, Hebei, Peoples R China
[2] Hebei Gen Hosp, Dept Haematol, 348 Heping West Rd, Shijiazhuang 050051, Hebei, Peoples R China
来源
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2024年 / 16卷 / 10期
关键词
T-LGLL; AIHA; IL-6; PTC; MGUS; MANIFESTATIONS; LGL; PATHOGENESIS; NEUTROPENIA;
D O I
10.62347/URFI7647
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:5735 / 5742
页数:8
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