Anterior scleritis with IgG4 lymphoplasmacytic infiltration: a case report.

IF 2.3 Q1 OPHTHALMOLOGY
Poojitha Balakrishnan, Matthew G Vicinanzo, John P Luckett, Tom Winokur, Ryan S Weldon, Russell W Read
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引用次数: 0

Abstract

Purpose: To report a case of chronic unilateral nodular anterior scleritis as a rare, isolated presentation of IgG4-related ophthalmic disease.

Case: A fifty-two-year-old patient was evaluated for painful, nodular scleral injection of the right eye, diagnosed as nodular anterior scleritis. There was only a partial response to topical corticosteroid and systemic immunomodulatory therapy. This, in combination with a sharp delineation between normal and abnormal sclera lead to the decision to perform a diagnostic biopsy of the lesion. Histopathology showed an IgG4 lymphoplasmacytic infiltration of the scleral tissue.

Conclusions: There are few documented reports of scleritis as the presenting manifestation of IgG4-related disease. IgG4-related disease is an increasingly recognized etiology to be considered in evaluating and managing scleritis.

前巩膜炎伴IgG4淋巴浆细胞浸润1例。
目的:报告一例慢性单侧结节性前巩膜炎,这是一种罕见的、孤立的igg4相关眼科疾病。病例:一名52岁的患者因右眼疼痛,结节性巩膜注射而被评估,诊断为结节性前巩膜炎。局部皮质类固醇和全身免疫调节治疗只有部分反应。结合正常和异常巩膜的清晰划分,决定对病变进行诊断性活检。组织病理学显示巩膜组织IgG4淋巴浆细胞浸润。结论:以igg4相关疾病为主要表现的巩膜炎文献报道很少。igg4相关疾病是一种越来越被认可的病因,在评估和治疗巩膜炎时需要考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.80
自引率
3.40%
发文量
39
审稿时长
13 weeks
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