Muhammad Abumanhal, Ran Ben Cnaan, Igal Leibovitch
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引用次数: 0
Abstract
Introduction: VEXAS syndrome (VEXAS - Vascular E, X-linked, A Autoinflammatory, S Somatic) is an adult-onset autoinflammatory disease caused by a somatic mutation in the E1 enzyme of the ubiquitin, encoded by the UBA1 gene, primarily affecting males. The syndrome is typically accompanied by hematologic disorders, mainly myelodysplastic syndrome. Additionally, it includes systemic manifestations such as lung nodules inflammation (alveolitis), recurrent infections, systemic fever, sinus and ear inflammations, and skin rashes. In this article, we present a case of a patient diagnosed with VEXAS syndrome following ocular involvement. Furthermore, we will review ocular manifestations described in the literature.
简介:VEXAS综合征(VEXAS - Vascular E, X-linked, A Autoinflammatory, S Somatic)是一种成人发病的自身炎症性疾病,由UBA1基因编码的泛素E1酶的体细胞突变引起,主要影响男性。该综合征通常伴有血液学疾病,主要是骨髓增生异常综合征。此外,它还包括全身性表现,如肺结节性炎症(肺泡炎)、复发性感染、全身性发热、鼻窦和耳部炎症以及皮疹。在这篇文章中,我们提出了一个病例的病人诊断为VEXAS综合征后,眼部受累。此外,我们将回顾文献中描述的眼部表现。