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首页> 外文期刊>Clinical and experimental rheumatology >Anterior ischaemic optic neuropathy in eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome):a case report and review of the literature
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Anterior ischaemic optic neuropathy in eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome):a case report and review of the literature

机译:嗜酸性肉芽肿合并多血管炎(Churg-Strauss综合征)的前部缺血性视神经病变:一例病例并文献复习

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We report a 62-year-old man with mild fever, headache and acute visual loss in his right eye due to anterior ischaemic optic neuropathy (AION), followed a few days later by pain in the legs and left arm associated with numbness and weakness.Giant cell arteritis complicated by AION was suspected at the beginning and high-dose oral glucocorticoids were started. However, on the basis of the past medical history of nasal poly-posis, asthma, and hypereosynophilia as well as of further investigations (biopsy of the nasal mttcosa showing granulomatous inflammation with a rich eosinophilic infiltrate, electromyo-graphy demonstrating, mononeuritis multiplex and positive p-ANCA), eosinophilic granulomatosis with polyangiitis (EGPA), previously known as Churg-Strauss syndrome, was diagnosed. Because visual acuity in the right eye deteriorated despite glucocorticoid therapy, pulse intravenous cyclophos-phamide was started, subsequently replaced by oral azathioprine, while prednisone was slowly tapered. This treatment led to gradual improvement of the neurological symptoms, whereas the right visual impairment remained unchanged.EGPA-related AION is an uncommon lesion that is probably due to vasculitic involvement of posterior ciliary and/ or chorioretinal arteries. The prognosis of established AION is poor for the affected eye, even when glucocorticoid treatment is started immediately. However, early recognition of AION and prompt aggressive treatment with high-dose glucocorticoids plus cyclophos-phamide can prevent visual loss in the unaffected eye.
机译:我们报告了一个62岁的男性,由于前部缺血性视神经病变(AION),其右眼出现轻度发烧,头痛和急性视力丧失,几天后,腿和左臂疼痛伴有麻木和无力一开始怀疑是并发AION的巨细胞动脉炎,并开始了大剂量口服糖皮质激素的治疗​​。但是,根据过去的鼻息肉病,哮喘和嗜酸性粒细胞增多病史以及进一步的研究(鼻粘膜活检显示肉芽肿性炎症,嗜酸性粒细胞浸润丰富,肌电图显示,单发性神经炎多发且阳性)诊断为嗜酸性肉芽肿合并多血管炎(EGPA),以前称为Churg-Strauss综合征。尽管进行了糖皮质激素治疗,但由于右眼视力下降,因此开始使用脉冲式静脉内环磷酰胺,随后由口服硫唑嘌呤代替,而泼尼松逐渐减量。这种治疗导致神经系统症状的逐渐改善,而右侧视力障碍保持不变。EGPA相关的AION是一种罕见的病变,可能是由于睫状后和/或脉络膜视网膜动脉的血管侵犯所致。即使立即开始糖皮质激素治疗,对于受影响的眼睛,已建立的AION的预后也很差。但是,尽早识别出AION并立即进行大剂量糖皮质激素加环磷酰胺的积极治疗可以防止未受影响的眼睛出现视力下降。

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