非血缘脐血移植后兼有温冷双抗体Evans综合征1例并文献复习

时月, 孙艳花, 李乾鹏, 等. 非血缘脐血移植后兼有温冷双抗体Evans综合征1例并文献复习[J]. 临床血液学杂志, 2024, 37(3): 210-213. doi: 10.13201/j.issn.1004-2806.2024.03.013
引用本文: 时月, 孙艳花, 李乾鹏, 等. 非血缘脐血移植后兼有温冷双抗体Evans综合征1例并文献复习[J]. 临床血液学杂志, 2024, 37(3): 210-213. doi: 10.13201/j.issn.1004-2806.2024.03.013
SHI Yue, SUN Yanhua, LI Qianpeng, et al. Evans syndrome with both warm and cold antibodies after umbilical cord blood transplantation: a case report and literature review[J]. J Clin Hematol, 2024, 37(3): 210-213. doi: 10.13201/j.issn.1004-2806.2024.03.013
Citation: SHI Yue, SUN Yanhua, LI Qianpeng, et al. Evans syndrome with both warm and cold antibodies after umbilical cord blood transplantation: a case report and literature review[J]. J Clin Hematol, 2024, 37(3): 210-213. doi: 10.13201/j.issn.1004-2806.2024.03.013

非血缘脐血移植后兼有温冷双抗体Evans综合征1例并文献复习

详细信息

Evans syndrome with both warm and cold antibodies after umbilical cord blood transplantation: a case report and literature review

More Information
  • Evans综合征国内外报道较为少见,兼有温冷双抗体Evans综合征更为罕见。文章报道了1例重型再生障碍性贫血患者行首次非血缘脐血移植后发生植入失败,再次输入非血缘脐血植入后病毒感染下引发兼有温冷双抗体Evans综合征,给予利妥昔单抗联合血浆置换治疗后患者各项指标均明显好转。笔者建议对于移植后早期并发Evans综合征的患者在给予传统方案治疗效果差时,应尽早考虑血浆置换和利妥昔单抗的联合和序贯应用。
  • 加载中
  • [1]

    韦若文, 陈文兰, 谢荣, 等. 伊布替尼治疗造血干细胞移植后自身免疫性血细胞减少2例报告并文献复习[J]. 第三军医大学学报, 2021, 43(21): 2337-2342. https://www.cnki.com.cn/Article/CJFDTOTAL-DSDX202121008.htm

    [2]

    郭毅刚, 肖青, 冯雪连, 等. 自体外周血造血干细胞移植术治疗淋巴瘤44例疗效分析[J]. 重庆医科大学学报, 2014, 39(1): 116-120. https://www.cnki.com.cn/Article/CJFDTOTAL-ZQYK201401031.htm

    [3]

    Patten E, Reuter FP. Evans'syndrome: possible benefit from plasma exchange[J]. Transfusion, 1980, 20(5): 589-593. doi: 10.1046/j.1537-2995.1980.20581034517.x

    [4]

    杜志丛, 赵艳丽, 曹星玉, 等. 单倍型供者造血干细胞移植治疗重型再生障碍性贫血的单中心研究[J]. 临床血液学杂志, 2023, 36(5): 366-372. https://lcxy.whuhzzs.com/article/doi/10.13201/j.issn.1004-2806.2023.05.013

    [5]

    张旭晗. 脐血移植治疗急性白血病后疗效与免疫重建和T细胞受体库变化的研究[D]. 济南: 山东大学, 2022.

    [6]

    Daikeler T, yndall A. Autoimmunity following haematopoietic stem-cell transplantation[J]. Best Pract Res Clin Haematol, 2007, 20(2): 349-360. doi: 10.1016/j.beha.2006.09.008

    [7]

    Hwang-Bo S, Kim SK, Lee JW, et al. Treatment and response of autoimmune cytopenia occurring after allogeneic hematopoietic cell transplantation in children[J]. Blood Res, 2017, 52(2): 119-124. doi: 10.5045/br.2017.52.2.119

    [8]

    Fattizzo B, Michel M, Giannotta JA, et al. Evans syndrome in adults: an observational multicenter study[J]. Blood Adv, 2021, 5(24): 5468-5478. doi: 10.1182/bloodadvances.2021005610

    [9]

    Blombery P, Kivivali L, Pepperell D, et al. Diagnosis and management of thrombotic thrombocytopenic purpura(TTP)in Australia: findings from the first 5 years of the Australian TTP/thrombotic microangiopathy registry[J]. Intern Med J, 2016, 46(1): 71-79. doi: 10.1111/imj.12935

    [10]

    Balassa K, Andrikovics H, Remenyi P, et al. The potential role of HLA-DRB1*11 in the development and outcome of haematopoietic stem cell transplantation-associated thrombotic microangiopathy[J]. Bone Marrow Transplant, 2015, 50(10): 1321-1325. doi: 10.1038/bmt.2015.161

    [11]

    Al-Nouri ZL, Reese JA, Terrell DR, et al. Drug-induced thrombotic microangiopathy: a systematic review of published reports[J]. Blood, 2015, 125(4): 616-618. doi: 10.1182/blood-2014-11-611335

    [12]

    Scully M. Thrombocytopenia in hospitalized patients: approach to the patient with thrombotic microangiopathy[J]. Hematology Am Soc Hematol Educ Program, 2017, 2017(1): 651-659. doi: 10.1182/asheducation-2017.1.651

    [13]

    祝宁宁, 胡慧瑾, 赵越超, 等. 利妥昔单抗治疗造血干细胞移植术后早期并发自身免疫性溶血性贫血1例并文献复习[J]. 中国现代医生, 2021, 59(11): 142-146. https://www.cnki.com.cn/Article/CJFDTOTAL-ZDYS202111037.htm

    [14]

    Pariente A, Joffre J, Fain O, et al. Plasma Exchanges for Refractory Evans Syndrome[J]. Ther Apher Dial, 2018, 22(5): 560-562.

    [15]

    Toussaint-Hacquard M, Coppo P, Soudant M, et al. Type of plasma preparation used for plasma exchange and clinical outcome of adult patients with acquired idiopathic thrombotic thrombocytopenic purpura: a French retrospective multicenter cohort study[J]. Transfusion, 2015, 55(10): 2445-2451. doi: 10.1111/trf.13229

    [16]

    曹星玉, 吴彤, 张耀臣, 等. 异基因造血干细胞移植后同时发生纯红细胞再生障碍性贫血和EVANS综合征1例并文献复习[J]. 临床血液学杂志, 2010, 23(9): 520-522. https://www.cnki.com.cn/Article/CJFDTOTAL-LCXZ201009006.htm

    [17]

    Miller PDE, Snowden JA, De Latour RP, et al. Autoimmune cytopenias(AIC)following allogeneic haematopoietic stem cell transplant for acquired aplastic anaemia: a joint study of the Autoimmune Diseases and Severe Aplastic Anaemia Working Parties(ADWP/SAAWP)of the European Society for Blood and Marrow Transplantation(EBMT)[J]. Bone Marrow Transplant, 2020, 55(2): 441-451. doi: 10.1038/s41409-019-0680-4

    [18]

    Blennerhassett R, Sudini L, Gottlieb D, et al. Post-allogeneic transplant Evans syndrome successfully treated with daratumumab[J]. Br J Haematol, 2019, 187(2): e48-e51.

    [19]

    Richard S, Fruchtman S, Scigliano E, et al. An immunological syndrome featuring transverse myelitis, Evans syndrome and pulmonary infiltrates after unrelated bone marrow transplant in a patient with severe aplastic anemia[J]. Bone Marrow Transplant, 2000, 26(11): 1225-1228. doi: 10.1038/sj.bmt.1702677

    [20]

    Winiarski J, Ringden O, Remberger M, et al. Bone marrow transplantation in children using unrelated donors at Huddinge Hospital[J]. Acta Paediatr, 1996, 85(3): 327-335. doi: 10.1111/j.1651-2227.1996.tb14026.x

  • 加载中
计量
  • 文章访问数:  298
  • PDF下载数:  13
  • 施引文献:  0
出版历程
收稿日期:  2023-05-19
刊出日期:  2024-03-01

目录