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Editorial: Wegener's Granulomatosis: More than Meets the Eye

机译:社论:韦格纳肉芽肿病:比目光更远

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Not so long ago I received a call from a distraught rheu-1 N matologist from a neighboring state about a patient with Wegener's granulomatosis who had just been diagnosed with retinal vasculitis by an ophthalmologist. Initially this patient had presented with orbital inflammatory disease, a known association with Wegener's, that is well reviewed by Pakrou and colleagues in this issue of Seminars in Arthritis and Rheumatism. Despite the appropriate use of cyclophosphamide, 1 eye had been enucleated due to the orbital inflammation. The ANCA titer, however, had become negative and the systemic disease was seemingly under excellent control with a low dose of daily, oral cyclophosphamide. Why then this sudden turn of events in the 1 remaining eye? Was the Wegener's reactivating despite the control of the vasculitis elsewhere in the body?
机译:不久前,我收到了来自邻邦的一位忧心aught的rheu-1 N放射科医生的电话,询问一位刚被眼科医生诊断为视网膜血管炎的韦格纳肉芽肿病患者。最初,该患者患有眼眶炎性疾病,这是与韦格纳氏症的一种已知关联,在本期关节炎与风湿病研讨会上,Pakrou及其同事对此进行了很好的评估。尽管适当使用环磷酰胺,但由于眼眶发炎,已摘除1只眼。然而,ANCA滴度已变为阴性,并且似乎通过每天口服小剂量环磷酰胺的良好控制,全身疾病得到了控制。为什么在剩下的1只眼中突然发生这种事件呢?尽管控制了身体其他部位的血管炎,但韦格纳会重新开始吗?

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