Garzón-Recalde Diego Alejandro, Rentería-Castillo Elizabeth, Anda-Garay Juan Carlos
Instituto Mexicano del Seguro Social, Centro Médico Nacional Siglo XXI, Hospital de Especialidades "Dr. Bernardo Sepúlveda Gutiérrez", Servicio de Medicina Interna. Ciudad de México, México.
Instituto Mexicano del Seguro Social, Hospital General de Zona 2-A "Francisco del Paso y Troncoso", Servicio de Hematología. Ciudad de México, México.
Rev Med Inst Mex Seguro Soc. 2024 Jan 8;62(1):1-7. doi: 10.5281/zenodo.10278179.
Cold agglutinin syndrome (CAS) is a hemolytic anemia mediated by antibodies, mainly IgM, whose maximum activity occurs at 4 °C. It happens secondary to infectious, autoimmune or neoplastic diseases, due to the formation of antibodies that cross-react against erythrocyte antigens, particularly of the I system. Here, we describe a case of CAS associated to Epstein-Barr virus (EBV) reactivation in a patient with primary human immunodeficiency virus (HIV) infection.
22-year old man with no medical history, hospitalized due to mononucleosis and anemic syndrome. Hemoglobin of 3.7 g/dL and elevation of lactate dehydrogenase were documented. In the peripheral blood smear it was observed spherocytosis, polychromasia and nucleated erythrocytes. EBV infection was confirmed with serology and viral load, as well as seronegative HIV infection with positive viral load. The C3d monospecific direct antiglobulin test was positive and an irregular antibody screening revealed the presence of an anti-I antibody. The patient received transfusion support and conservative treatment, with remission of the symptoms 2 weeks after admission.
Cold agglutinin syndrome is a rare, potentially fatal complication of infectious mononucleosis, which should be considered in the face of findings suggestive of hemolysis in order to initiate support measures in a timely manner.
冷凝集素综合征(CAS)是一种由抗体介导的溶血性贫血,主要为IgM抗体,其最大活性出现在4℃。它继发于感染性、自身免疫性或肿瘤性疾病,是由于形成了与红细胞抗原(特别是I系统抗原)发生交叉反应的抗体。在此,我们描述了一例原发性人类免疫缺陷病毒(HIV)感染患者中与爱泼斯坦-巴尔病毒(EBV)重新激活相关的CAS病例。
一名22岁无病史男性,因单核细胞增多症和贫血综合征住院。记录到血红蛋白为3.7 g/dL,乳酸脱氢酶升高。在外周血涂片上观察到球形红细胞增多、嗜多色性和有核红细胞。通过血清学和病毒载量证实了EBV感染,以及病毒载量阳性的HIV血清阴性感染。C3d单特异性直接抗球蛋白试验呈阳性,不规则抗体筛查显示存在抗I抗体。患者接受了输血支持和保守治疗,入院2周后症状缓解。
冷凝集素综合征是传染性单核细胞增多症一种罕见的、潜在致命的并发症,面对提示溶血的发现时应予以考虑,以便及时启动支持措施。