Orbital Inflammatory Complications of Crohn's Disease: A Rare Case Series.

Clinical Medicine Insights. Gastroenterology Pub Date : 2018-02-20 eCollection Date: 2018-01-01 DOI:10.1177/1179552218757512
Tanya M Monaghan, Giorgio Albanese, Philip Kaye, James D Thomas, Lorraine C Abercrombie, Gordon W Moran
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引用次数: 6

Abstract

Orbital inflammatory disease is a rare ophthalmic manifestation of Crohn's disease. Inflammation is characteristically nonspecific, involving one or multiple structures of the orbit. Mechanisms of disease and optimal methods of treatment are poorly understood. The aim of this report is to present 3 cases of orbital involvement in Crohn's disease. A retrospective case note review of patients with orbital inflammatory disease and Crohn's disease was performed at our academic center to determine the clinical, imaging, and histopathologic features of this condition and its relationship to intestinal Crohn's disease. Three patients were identified with orbital inflammatory manifestations complicating Crohn's disease. All patients described were women with active intestinal disease and had a history of treatment with immunosuppressive therapies. Similarities were observed in clinical presentations with variance noted in radiologic and histopathologic findings. In all cases, symptoms improved with oral corticosteroids or nonsteroidal drugs in combination with anti-tumor necrosis factor agents. Inflammatory bowel disease-related orbital complications are rare but potentially vision-threatening. It is important to consider mimics of orbital inflammatory disease such as systemic inflammatory disease, malignancy, congenital malformations, infection, and trauma when formulating a comprehensive differential diagnosis. Therapeutic intervention is directed toward preservation of vision and orbital function and reducing the acute inflammatory process. Corticosteroids are typically the initial treatment of choice for moderate-to-severe disease, although several classes of immunomodulatory agents have been variably useful in treating this condition. Heightened awareness and close cooperation between gastroenterologists and ophthalmologists are mandatory.

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克罗恩病的眼眶炎症并发症:罕见病例系列
眼窝炎是克罗恩病罕见的眼部表现。炎症的特征是非特异性的,可累及眼眶的一个或多个结构。疾病的机制和最佳治疗方法尚不清楚。本报告的目的是提出3例眼窝受累在克罗恩病。在我们的学术中心对眼眶炎症性疾病和克罗恩病患者进行回顾性病例回顾,以确定该疾病的临床、影像学和组织病理学特征及其与肠道克罗恩病的关系。3例患者被确定为眼窝炎症表现并发克罗恩病。所有描述的患者均为患有活动性肠道疾病的女性,并有免疫抑制治疗史。临床表现相似,但放射学和组织病理学表现不同。在所有病例中,口服皮质类固醇或非甾体类药物联合抗肿瘤坏死因子药物可改善症状。炎症性肠病相关的眼眶并发症是罕见的,但潜在的视力威胁。在制定全面的鉴别诊断时,重要的是要考虑眼眶炎性疾病的模拟物,如全身性炎性疾病、恶性肿瘤、先天性畸形、感染和创伤。治疗干预的目的是保护视力和眼眶功能,减少急性炎症过程。皮质类固醇通常是中重度疾病的首选初始治疗,尽管有几种类型的免疫调节剂对治疗这种疾病有不同的作用。胃肠病学家和眼科医生之间必须提高认识并密切合作。
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
Clinical Medicine Insights. Gastroenterology
Clinical Medicine Insights. Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
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