Steinberg A D, Seldin M F, Jaffe E S, Smith H R, Klinman D M, Krieg A M, Cossman J
National Institutes of Health, Bethesda, MD 20892.
Ann Intern Med. 1988 Apr;108(4):575-84. doi: 10.7326/0003-4819-108-4-575.
Angioimmunoblastic lymphadenopathy with dysproteinemia is a disorder characterized by a sudden onset of constitutional symptoms and lymphadenopathy. Patients often have hypergammaglobulinemia, autoantibodies, rashes, thrombocytopenia, or hemolytic anemia. Diagnosis requires a lymph node biopsy that shows architectural effacement, absence of germinal centers, arborization of postcapillary venules, and a polymorphous infiltrate that includes immunoblasts. Early in the disease, activated T cells in blood and lymph nodes stimulate B cells to proliferate and produce antibody. However, late in the disease, immune suppression may result from increased suppressor function. Clonal rearrangements, which are seen in all patients with regard to either the T-cell receptor beta-chain gene or immunoglobulin genes, have been followed by malignant transformation and frank lymphoma in some patients. Thus, this disorder stands partway between benign lymphoid proliferation and clonal lymphoid transformation. The prognosis of this disorder is poor; 75% of patients die within 2 years or develop a lymphoid malignancy. The rest usually go into a sustained remission. Current treatment with corticosteroid and immunosuppressive agents is unsatisfactory, especially because of late immunosuppression and predisposition to infections.
血管免疫母细胞性淋巴结病伴蛋白异常血症是一种以全身症状和淋巴结病突然发作为特征的疾病。患者常伴有高丙种球蛋白血症、自身抗体、皮疹、血小板减少或溶血性贫血。诊断需要进行淋巴结活检,活检结果显示结构破坏、生发中心缺失、毛细血管后小静脉分支以及包括免疫母细胞在内的多形性浸润。在疾病早期,血液和淋巴结中的活化T细胞刺激B细胞增殖并产生抗体。然而,在疾病晚期,免疫抑制可能是由于抑制功能增强所致。在所有患者中,无论是T细胞受体β链基因还是免疫球蛋白基因都可见克隆重排,部分患者随后会发生恶性转化并发展为明显的淋巴瘤。因此,这种疾病处于良性淋巴增殖和克隆性淋巴转化之间。这种疾病的预后很差;75%的患者在2年内死亡或发展为淋巴恶性肿瘤。其余患者通常会进入持续缓解期。目前使用皮质类固醇和免疫抑制剂的治疗并不令人满意,特别是因为晚期免疫抑制和易感染的倾向。