Boissonnas A, Reboul M, Lemaigre G, Chapuis Y, Cachin M
Phlebologie. 1977 Jan-Mar;30(1):83-91.
This case of recurrent migratory superficial phlebitis is reported because of the highly unusual nature of the lesion observed. The picture was dominated by periphlebitis with inflammatory granuloma, giant cells and elastophagia. When the condition had been present for sixteen months, an aortic arch syndrome developed in an inflammatory context. In this light, various auto-immunological etiologies were considered, among them Takayashu's arteritis of which, in the author's opinion, this would be the first case to be combined with venopathy.
报道这例复发性游走性浅表静脉炎是因为所观察到的病变具有高度特殊性。病变主要表现为伴有炎性肉芽肿、巨细胞和弹力纤维吞噬的静脉周炎。在病情持续16个月后，在炎症背景下出现了主动脉弓综合征。鉴于此，考虑了各种自身免疫性病因，其中包括高安动脉炎，作者认为这将是首例合并静脉病变的高安动脉炎病例。
