Simu G, Macavei I
Morphol Embryol (Bucur). 1976 Jul-Sep;22(3):183-6.
Two patients with clinical and pathological symptoms of so-called angioimmunoblastic lymphadenitis are presented. Both patients were over 50, with multiple lymphadenopathies, fever, pruritus and hyperglobulinemia. The lymph node changes exhibited a characteristic histological triad consisting of diffuse lymphoid proliferation, small arborizing vessels proliferation and paraamyloid-like amorphous material deposition. As previous authors suggested, the disease seems to be the expression of a prolonged hyperimmune response induced by the hypersensitivity to certain factors.
本文报告了两名具有所谓血管免疫母细胞性淋巴结炎临床和病理症状的患者。两名患者均超过50岁，有多处淋巴结病、发热、瘙痒和高球蛋白血症。淋巴结变化呈现出一种特征性的组织学三联征，包括弥漫性淋巴样增生、小树枝状血管增生和类淀粉样无定形物质沉积。正如之前的作者所指出的，该病似乎是对某些因素过敏所引发的长期超敏反应的表现。
