Margolis Ron, Kosmorsky Gregory S, Lowder Careen Y, Schoenfield Lynn
Cole Eye Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
Ocul Immunol Inflamm. 2007 Mar-Apr;15(2):113-5. doi: 10.1080/09273940701299388.
To describe an unusual case of Churg-Strauss syndrome (CSS) that presented with a conjunctival nodule and was successfully treated with oral corticosteroids.
Case report.
A 30-year-old woman with a history of adult-onset asthma, seasonal allergies, and a lung mass presented with a nodular elevation of the conjunctiva. Excisional biopsy demonstrated necrotizing eosinophilic granulomas. Systemic evaluation revealed peripheral eosinophilia and elevated IgE, consistent with Churg-Strauss syndrome. The patient's symptoms and eosinophilia resolved after an increase in the dose of oral corticosteroids.
This case describes a unique presentation of conjunctival involvement in CSS that differs from prior case reports by having a small, well-demarcated nodule and lacking signs of active inflammation.
描述一例罕见的变应性肉芽肿性血管炎(CSS)病例,该病例以结膜结节为表现,经口服糖皮质激素治疗成功。
病例报告。
一名30岁女性,有成人发作性哮喘、季节性过敏和肺部肿块病史,出现结膜结节状隆起。切除活检显示坏死性嗜酸性肉芽肿。全身评估显示外周嗜酸性粒细胞增多和IgE升高,符合变应性肉芽肿性血管炎。增加口服糖皮质激素剂量后,患者的症状和嗜酸性粒细胞增多症得到缓解。
本病例描述了变应性肉芽肿性血管炎累及结膜的一种独特表现,与先前的病例报告不同,其表现为一个小的、边界清晰的结节,且无活动性炎症迹象。