Seigneurin J M, Mingat J, Lenoir G M, Couderc P, Micoud M
Br Med J (Clin Res Ed). 1981 May 16;282(6276):1574-5. doi: 10.1136/bmj.282.6276.1574.
Angioimmunoblastic lymphadenopathy occurred in a 46-year-old man 16 months after an episode of infectious mononucleosis induced by Epstein-Barr (EB) virus. The features of infectious mononucleosis included fever, pharyngitis, lymph gland enlargement, hepatosplenomegaly, hyperbasophilic mononuclear cells, and IgM antibodies to EB virus, although heterophile antibodies were not detected. The illness was severe and prolonged and included an asymptomatic measles virus infection. Over a year later massive enlargement of the lymph nodes led to a biopsy, which showed a diffuse infiltration with lymphoid cells and a proliferation of arborising small vessels typical of angioimmunoblastic lymphadenopathy. In spite of corticosteroids, levamisole, chlorambucil, and radiotherapy, no remission occurred, and serious infections led to death 18 months after the onset. Viral infections with EB virus and measles virus associated with pre-existing or subsequent immunological changes probably resulted in the appearance of angioimmunoblastic lymphadenopathy.
血管免疫母细胞性淋巴结病发生在一名46岁男性身上,该患者在由爱泼斯坦-巴尔(EB)病毒引起的传染性单核细胞增多症发作16个月后发病。传染性单核细胞增多症的特征包括发热、咽炎、淋巴结肿大、肝脾肿大、嗜碱性增强的单核细胞以及针对EB病毒的IgM抗体,不过未检测到嗜异性抗体。病情严重且持续时间长,还包括一次无症状的麻疹病毒感染。一年多后,淋巴结大量肿大,遂进行活检,结果显示有淋巴细胞弥漫性浸润以及血管免疫母细胞性淋巴结病典型的分支状小血管增生。尽管使用了皮质类固醇、左旋咪唑、苯丁酸氮芥和放疗,病情仍未缓解,严重感染导致患者在发病18个月后死亡。与先前存在或随后发生的免疫变化相关的EB病毒和麻疹病毒感染可能导致了血管免疫母细胞性淋巴结病的出现。