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Relapsing Polychondritis

机译:复发性多发性软骨炎

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摘要

Relapsing polychondritis (RP) is a rare systemic disease characterized by recurrent, widespread chondritis of the auricular, nasal, and tracheal cartilages. Additional clinical features include audiovestibular dysfunction, ocular inflammation, vasculitis, myocarditis, and nonerosive arthritis. Although the cause remains unknown, the etiology is suspected to be autoimmune. We describe a case of a 31-year-old woman with a four-month history of bilateral auricular and nasal chondritis. Infectious and neoplastic diseases were excluded by imaging and laboratory examinations. RP was diagnosed based on three McAdam's criteria. The patient was medicated with oral prednisolone and methotrexate with positive clinical response. In this case clinical history and detailed physical examination were fundamental in concluding the correct diagnosis and administrating the appropriate medication.
机译:复发性多发性软骨炎(RP)是一种罕见的全身性疾病,其特征是耳,鼻和气管软骨复发性,广泛性软骨炎。其他临床特征包括听力前庭功能障碍,眼部炎症,血管炎,心肌炎和非侵蚀性关节炎。尽管原因尚不清楚,但病因被怀疑是自身免疫性的。我们描述了一个病例,该病例为一名31岁的妇女,其双耳和鼻软骨炎的病史为四个月。影像学和实验室检查排除了传染性和肿瘤性疾病。 RP是根据McAdam的三个标准诊断的。该患者接受口服泼尼松龙和甲氨蝶呤的药物治疗,临床反应良好。在这种情况下,临床历史和详细的体格检查是得出正确诊断和给予适当药物的基础。

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