Wongsaengsak Sariya, Czader Magdalena, Suvannasankha Attaya
Division of Hematology and Oncology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
BMJ Case Rep. 2018 Jul 10;2018:bcr-2017-222064. doi: 10.1136/bcr-2017-222064.
Cold agglutinin-mediated autoimmune haemolytic anaemia is associated with the development of autoantibodies that can agglutinate red blood cells at cold temperatures. While primary cold agglutinin disease is an idiopathic lymphoproliferative disorder, secondary cold agglutinin syndrome (CAS) complicates other diseases such as infections, autoimmune diseases and cancers, mostly low-grade lymphomas. Early recognition, treatment of CAS and treatment of its associated underlying diseases are crucial to a successful outcome. We report a case of CAS in a setting of diffuse large B cell lymphoma, in which the treatment course was complicated by worsened anaemia due to chemotherapy-induced myelosuppression. We reviewed previously reported cases and discussed diagnosis and treatment strategies, including novel complement inhibitors, as potential future therapy.
冷凝集素介导的自身免疫性溶血性贫血与可在低温下凝集红细胞的自身抗体的产生有关。原发性冷凝集素病是一种特发性淋巴增殖性疾病,而继发性冷凝集素综合征(CAS)会使其他疾病如感染、自身免疫性疾病和癌症(主要是低度淋巴瘤)复杂化。早期识别、治疗CAS及其相关的基础疾病对于取得成功的治疗结果至关重要。我们报告了1例弥漫性大B细胞淋巴瘤患者发生CAS的病例,该患者的治疗过程因化疗引起的骨髓抑制导致贫血加重而变得复杂。我们回顾了先前报道的病例,并讨论了诊断和治疗策略,包括新型补体抑制剂作为潜在的未来治疗方法。