Teh L S, O'Connor G M, O'Sullivan M M, Pandit J C, Beck L, Williams B D
Department of Rheumatology, University Hospital of Wales, Heath Park, Cardiff.
Ann Rheum Dis. 1990 Jun;49(6):410-1. doi: 10.1136/ard.49.6.410.
Two patients with Behçet's syndrome and intracranial hypertension are reported. One developed a recurrence of papilloedema while receiving treatment but eventually made a full recovery, whereas the other developed optic atrophy within three months of onset despite treatment.
报告了两名患有白塞病和颅内高压的患者。其中一名在接受治疗时视乳头水肿复发,但最终完全康复,而另一名尽管接受了治疗,但在发病后三个月内出现了视神经萎缩。