眼眶表现嗜酸性肉芽肿病伴多血管炎:一例介入病例报告及文献复习。

IF 1.5 Q3 OPHTHALMOLOGY
Journal of Ophthalmic & Vision Research Pub Date : 2025-08-27 eCollection Date: 2025-01-01 DOI:10.18502/jovr.v20.16399
Ozlem Barut Selver, Emil Ahmadli, Muhammed Dara Tas, Banu Yaman, Naim Ceylan, Mozhgan Rezaei Kanavi
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引用次数: 0

摘要

目的:报告一例嗜酸性肉芽肿病合并多血管炎(EGPA),最初表现为眼眶受累,描述其成功的治疗方法,并提供全面的文献回顾。病例报告:一名33岁女性患者,表现为左上眼睑肿胀、发红、压痛及肿块一个月。上眼睑外翻在同一区域的结膜下可见多分叶状病变。患者病史包括哮喘和房间隔缺损手术。眼眶MRI显示软组织肿块浸润前眼眶上外侧及眶外,并向眶前区延伸。病变进行了切口活检,组织病理学结果与EGPA的诊断一致。病人的血液检查显示嗜酸性粒细胞增多和抗中性粒细胞细胞质抗体阴性。在排除了其他类似的病理,如肉芽肿病合并多血管炎后,我们观察到她的眼眶病变在全身类固醇治疗后显著消退。结论:EGPA的诊断是一种罕见的临床表现,对眼科医生来说至关重要,因为它提供了对全身性疾病的早期识别,并可以通过及时开始适当的治疗来帮助减缓其进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Orbital Presentation of Eosinophilic Granulomatosis with Polyangiitis: An Interventional Case Report and Literature Review.

Orbital Presentation of Eosinophilic Granulomatosis with Polyangiitis: An Interventional Case Report and Literature Review.

Orbital Presentation of Eosinophilic Granulomatosis with Polyangiitis: An Interventional Case Report and Literature Review.

Purpose: To report a case of eosinophilic granulomatosis with polyangiitis (EGPA) initially presenting as orbital involvement, describe its successful management, and provide a comprehensive literature review.

Case report: A 33-year-old female patient presented with swelling, redness, tenderness, and a mass under the left upper eyelid for one month. Upper lid eversion showed a multilobulated lesion in the subconjunctival area of the same region. The patient's medical history included asthma and atrial septal defect surgery. Orbital MRI revealed a soft tissue mass infiltrating the superior and lateral aspects of the conal and extraconal regions in the anterior orbit, with extension toward the preseptal area. The lesion underwent incisional biopsy, and histopathological findings were consistent with the diagnosis of EGPA. The patient's blood tests revealed eosinophilia and a negative antineutrophil cytoplasmic antibody. After excluding other similar pathologies such as granulomatosis with polyangiitis, we observed a dramatic regression in her orbital lesion following systemic steroid therapy.

Conclusion: The diagnosis of EGPA, a rare clinical presentation, is crucial for ophthalmologists because it provides early recognition of the systemic disease and can help slow its progression by initiating appropriate treatment in a timely manner.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
63
审稿时长
30 weeks
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