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首页> 外文期刊>American journal of otolaryngology >Features of coexisting granulomatosis with polyangiitis in a patient with pemphigus vulgaris: a case report
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Features of coexisting granulomatosis with polyangiitis in a patient with pemphigus vulgaris: a case report

机译:寻常型天疱疮患者肉芽肿合并多血管炎的特征:一例报告

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摘要

Pemphigus vulgaris (PV) and granulomatosis with polyangiitis (Wegener's or GPA) are two rare autoimmune disorders. Both can involve the upper airways, and diagnosis can be difficult in the absence of extra-airway symptoms. We report the case of a patient with well-controlled PV but persistent upper respiratory tract symptoms. Further evaluation revealed perforation of the nasal septum and elevated serologies consistent with GPA. The patient improved with rituximab treatments. This case demonstrates that alternative concomitant diagnosis should be considered in patients with symptoms suggestive of recalcitrant PV and/or GPA, since these patients may require more aggressive initial treatment. (C) 2015 Elsevier Inc. All rights reserved.
机译:寻常性天疱疮(PV)和肉芽肿合并多血管炎(Wegener或GPA)是两种罕见的自身免疫性疾病。两者都可能累及上呼吸道,并且在没有气道外症状的情况下可能难以诊断。我们报告一例患者,其PV控制良好,但持续出现上呼吸道症状。进一步评估显示鼻中隔穿孔和血清学升高,符合GPA。利妥昔单抗治疗使患者好转。该病例表明,对于症状提示顽固性PV和/或GPA的患者,应考虑其他伴随诊断,因为这些患者可能需要更积极的初始治疗。 (C)2015 Elsevier Inc.保留所有权利。

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