复发性眶上裂综合征与VEXAS综合征相关。

IF 2.9 Q1 OPHTHALMOLOGY
Katie Myint, Namritha Patrao, Oana Vonica, Kaveh Vahdani
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引用次数: 0

摘要

目的:报道一例复发性眶炎和眶上裂综合征合并VEXAS(空泡,E1酶,x连锁,自身炎症,躯体)综合征的病例。病例介绍:VEXAS综合征是最近发现的一种多系统炎症性疾病,发病晚于成人。作者描述了一个76岁的男子谁提出了反复发作的眶炎,眶上裂综合征,泪腺炎和眶肌炎。他有一系列全身性疾病,包括复发性胸部感染、充血性心力衰竭、肺栓塞和皮疹。通过基因检测证实了VEXAS综合征的潜在诊断,发现了UBA1突变。结论:眼眶炎性疾病合并多系统炎性疾病的鉴别诊断应考虑VEXAS综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recurrent superior orbital fissure syndrome associated with VEXAS syndrome.

Purpose: To describe a case of recurrent orbital inflammation and superior orbital fissure syndrome associated with VEXAS (vacuoles, E1 enzyme, X-linked, auto-inflammatory, somatic) syndrome.

Case presentation: VEXAS syndrome is a recently identified multi-system inflammatory disease of late adult onset. The authors describe the case of a 76-year-old man who presented with recurrent episodes of orbital inflammation, with superior orbital fissure syndrome, dacryoadenitis and orbital myositis. He had a constellation of systemic disorders including recurrent chest infections, congestive cardiac failure, pulmonary emboli and skin rashes. The underlying diagnosis of VEXAS syndrome was confirmed by genetic testing, which revealed the UBA1 mutation.

Conclusion: VEXAS syndrome should be considered in the differential diagnosis of orbital inflammatory disease associated with multi-system inflammatory disorders.

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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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