Bernengo M G, Levi L, Zina G
Br J Dermatol. 1981 Feb;104(2):131-9. doi: 10.1111/j.1365-2133.1981.tb00034.x.
Angioimmunoblastic lymphadenopathy with drysproteinaemia is reported (AILD) in four patients with different skin pictures. As the disease progresses two main forms predominate; papulonodular and erythroderma. In all cases the histological picture of the skin mirrors that of the lymph-node. Our results point to an increase in the peripheral blood, lymph-nodes and skin of T and subsequently of B lymphocytes suggesting that a proliferation of helper T cells and hence activation of the B-cell subpopulation may be involved in the pathogenesis of some cases of AILD.
本文报道了4例具有不同皮肤表现的血管免疫母细胞性淋巴结病伴低蛋白血症(AILD)患者。随着疾病进展,主要出现两种形式;丘疹结节型和红皮病型。在所有病例中,皮肤的组织学表现与淋巴结相似。我们的结果表明,T淋巴细胞随后是B淋巴细胞在外周血、淋巴结和皮肤中均增加,提示辅助性T细胞增殖以及B细胞亚群的激活可能参与了某些AILD病例的发病机制。