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Bilateral scleritis and sclerokeratitis associated with IgA nephropathy

机译:与IgA肾病相关的双侧巩膜炎和巩膜角膜炎

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The purpose of this study is to report a case of bilateral nodular scleritis in a patient with final diagnosis of IgA nephropathy. This is an observational case report. A male patient, 42?years old, presented with a bilateral nodular scleritis and OD sclerokeratitis. He had a previous history of acute otitis media and developed posterior renal failure and arterial hypertension. Clinical and systemic findings suggest Wegener's granulomatosis. A kidney biopsy was performed, and immunoflourescence findings demonstrated granular deposits of IgA in a mesangial pattern confirming the diagnosis of IgA nephropathy IgA nephropathy should be a differential diagnosis in patients with scleritis and nephropathy.
机译:这项研究的目的是报告最终诊断为IgA肾病的患者的双侧结节性巩膜炎病例。这是一个观察性病例报告。一名42岁的男性患者出现双侧结节性巩膜炎和OD巩膜角膜炎。他曾有急性中耳炎病史,并发展为后肾功能衰竭和动脉高压。临床和全身发现提示韦格纳肉芽肿病。进行了肾脏活检,免疫荧光结果显示肾小球系膜有IgA颗粒状沉积,从而证实了IgA肾病的诊断IgA肾病应作为硬化症和肾病患者的鉴别诊断。

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