Carbone J, Sarmiento E, Rodríguez-Molina J J, Fernández-Cruz E
Unidad de Inmunología Clínica, Servicio de Inmunología, Hospital General Universitario Gregorio Marañón, Spain.
Allergol Immunopathol (Madr). 2004 Jul-Aug;32(4):218-22. doi: 10.1016/s0301-0546(04)79242-3.
Common variable immunodeficiency (CVID) is a primary immunodeficiency disease, the hallmark of which is hypogammaglobulinemia and poor specific antibody responses. Patients usually have recurrent bacterial infections, but there are a number of other comorbid disorders, including autoimmune disease and neoplasms. Most patients are diagnosed as adults, and delay in identifying the antibody defect is common. In the present report, we illustrate atypical initial presentation without infections in CVID.
In 5 out of 30 patients with CVID (16.6 %) diagnosed in our hospital in the Autonomous Community of Madrid, the first manifestation of immunodeficiency was not an infection. Three patients presented with immune cytopenias (thrombocytopenic purpura [n = 2] and hemolytic anemia [n = 1]); one patient had pernicious anemia and one patient had insulin-dependent diabetes as the first clinical feature of CVID. Four patients had IgG levels below 400 mg/dl.
Atypical presentations of CVID must be recognized to prevent delayed diagnosis. Presentation of CVID as an autoimmune disease in the absence of recurrent infections prompts us to suggest baseline testing of immunoglobulin levels in patients presenting with autoimmune disorders.
普通可变型免疫缺陷(CVID)是一种原发性免疫缺陷疾病,其特征为低丙种球蛋白血症和特异性抗体反应不佳。患者通常反复发生细菌感染,但还存在许多其他合并症,包括自身免疫性疾病和肿瘤。大多数患者在成年期被诊断出来,抗体缺陷的识别延迟很常见。在本报告中,我们阐述了CVID中无感染的非典型初始表现。
在马德里自治区我们医院诊断的30例CVID患者中,有5例(16.6%)免疫缺陷的首发表现不是感染。3例患者表现为免疫性血细胞减少(血小板减少性紫癜[n = 2]和溶血性贫血[n = 1]);1例患者以恶性贫血为首发症状,1例患者以胰岛素依赖型糖尿病作为CVID的首个临床特征。4例患者的IgG水平低于400 mg/dl。
必须认识到CVID的非典型表现,以防止诊断延迟。在无反复感染的情况下,CVID表现为自身免疫性疾病,这促使我们建议对患有自身免疫性疾病的患者进行免疫球蛋白水平的基线检测。