尽管抗白介素-5受体治疗,但嗜酸性肉芽肿病合并多血管炎的发展:贝那利珠单抗治疗期间双侧视网膜中央动脉闭塞的第一例

IF 2.8 Q2 RHEUMATOLOGY
Elena Treppo, Lucia Finocchio, Benedetta Fazzi, Maria Pillon, Luca Quartuccio
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引用次数: 0

摘要

在这里,我们描述了一个罕见的嗜酸性肉芽肿病合并多血管炎(EGPA)在贝那利珠单抗治疗下表现为双侧视网膜中央动脉闭塞(CRAO)。患者为61岁男性,患有慢性嗜酸性鼻窦炎和严重哮喘,突然双侧视力丧失和短暂性黑朦。眼科检查,包括眼底检查和光学相干断层扫描,证实CRAO,实验室检查结果显示炎症标志物升高,在嗜酸性粒细胞计数正常的情况下,抗髓过氧化物酶抗体阳性。强化免疫抑制治疗导致全身性炎症消退,但仍存在明显的视力损害。这些发现强调了抗白细胞介素-5受体治疗在预防EGPA血管并发症方面的潜在局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development of Eosinophilic Granulomatosis With Polyangiitis Despite Anti-Interleukin-5 Receptor Therapy: The First Case of Bilateral Central Retinal Artery Occlusion During Benralizumab Treatment.

Development of Eosinophilic Granulomatosis With Polyangiitis Despite Anti-Interleukin-5 Receptor Therapy: The First Case of Bilateral Central Retinal Artery Occlusion During Benralizumab Treatment.

Here, we describe a rare presentation of eosinophilic granulomatosis with polyangiitis (EGPA) under benralizumab therapy manifesting as bilateral central retinal artery occlusion (CRAO). The patient, a 61-year-old man with chronic eosinophilic rhinosinusitis and severe asthma, experienced sudden bilateral visual loss and transient amaurosis. Ophthalmologic evaluations, including a fundus examination and optical coherence tomography, confirmed CRAO, and laboratory test results revealed elevated markers of inflammation and positive antimyeloperoxidase antibodies in the context of normal eosinophil counts. Intensive immunosuppressive therapy led to resolution of systemic inflammation, although significant visual impairment persisted. These findings underscore the potential limitations of anti-interleukin-5 receptor therapy in preventing vasculitic complications in EGPA.

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CiteScore
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