anca相关性血管炎的眼部表现

IF 0.3 4区 医学 Q4 Medicine Acta Medica Mediterranea Pub Date : 2021-11-22 DOI:10.32552/2021.actamedica.551
Merve İnanç Tekin, Müge Pınar Çakar Özdal
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引用次数: 1

摘要

抗中性粒细胞细胞质抗体相关血管炎的眼部表现可能与一般或有限形式的疾病有关,甚至可能在没有全身性疾病的情况下发生。相关血管炎的眼部表现可能是以前未表现或未诊断的全身性疾病的第一症状,使眼科医生有助于诊断。虽然其眼部表现是可变的和非特异性的,但坏死性改变和角膜周围受累伴有巩膜炎症是提示全身性血管炎,特别是相关血管炎的重要线索。这种疾病可能会影响眼睛的所有层;巩膜炎和眼眶受累是最常见的。结膜炎、外巩膜炎、周围性溃疡性角膜炎、葡萄膜炎和视网膜血管炎是在病程中可能观察到的其他眼部表现。眼部受累最常见于肉芽肿病合并多血管炎,其次是嗜酸性肉芽肿病合并多血管炎和显微镜下的多血管炎。由于相关血管炎的高发病率和死亡率,认识到血管炎的眼部表现是潜在全身性疾病的征兆和疾病活动的指标是非常重要的。治疗取决于眼部受累的位置和严重程度。虽然局部药物和手术治疗可以帮助控制相关的眼部疾病,但通常需要全身免疫抑制药物来控制潜在疾病。随着生物制剂的可用性和使用的增加,严重眼部并发症患者的预后得到改善。利妥昔单抗在伴有眼部相关血管炎的患者,特别是环磷酰胺耐药病例中,可有效诱导缓解和控制复发。为了取得成功的结果,需要在相关血管炎患者的诊断、治疗和随访方面采用多学科方法。
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Ophthalmic Manifestations of ANCA-Associated Vasculitis
Ocular manifestations in antineutrophil cytoplasmic antibody-associated vasculitis can be associated with the general or limited form of disease and can even occur in the absence of systemic disease. Ocular manifestations of associated vasculitis can be the first symptom of previously not manifested or undiagnosed systemic disease, allowing ophthalmologists to contribute to the diagnosis. Although its ocular findings are variable and nonspecific, the presence of necrotizing changes and peripheral corneal involvement accompanying scleral inflammation are important clues suggesting systemic vasculitis, especially associated vasculitis. The disease may affect all layers of the eye; scleritis and orbital involvement being the most common. Conjunctivitis, episcleritis, peripheral ulcerative keratitis, uveitis and retinal vasculitis are other ocular findings that may be observed during the disease course. Ocular involvement is most commonly seen in granulomatosis with polyangiitis followed by eosinophilic granulomatosis with polyangiitis and microscopic polyangiitis. Due to the high morbidity and mortality of associated vasculitis, it is very important to recognize the ocular manifestations of vasculitis as a sign of the underlying systemic disease and an indicator for the disease activity. Treatment varies depending on the location and severity of the ocular involvement. Although localized medical and surgical treatments can help to manage associated ocular disease, systemic immunosuppressive medications are often required to control the underlying disease. With the increasing availability and use of biological agents, prognosis has improved in patients with severe ocular complications. Rituximab appears to be useful in inducing remission and controlling relapses in patients with ocular involvement of associated vasculitis, particularly in cyclophosphamide resistant cases. A multidisciplinary approach in the diagnosis, treatment and follow-up of patients with associated vasculitis is required in order to achieve successful results.
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来源期刊
Acta Medica Mediterranea
Acta Medica Mediterranea 医学-医学:内科
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6-12 weeks
期刊介绍: Acta Medica Mediterranea is an indipendent, international, English-language, peer-reviewed journal, online and open-access, designed for internists and phisicians. The journal publishes a variety of manuscript types, including review articles, original research, case reports and letters to the editor.
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