Look granulomatosis with polyangiitis (GPA) straight in the face: missed opportunities leading to a delayed diagnosis.

Q1 Medicine Auto-Immunity Highlights Pub Date : 2019-09-17 eCollection Date: 2019-12-01 DOI:10.1186/s13317-019-0118-4
N Rolle, M Muruganandam, I Jan, F M Harji, J Harrington, K N Konstantinov
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Abstract

Granulomatosis with polyangiitis (GPA) is a systemic vasculitis with a potential to involve any organ system. It remains an important cause of kidney related morbidity and mortality. Early diagnosis can be difficult and requires high index of suspicion in all patients, but especially in cases with atypical presentation. We report a case with GPA, which was diagnosed only after new and advancing symptoms belied the original diagnosis of bilateral facial palsy and aortic mural thrombus.

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肉芽肿合并多血管炎(GPA)直接面对:错过机会导致延误诊断。
肉芽肿病伴多血管炎(GPA)是一种可能累及任何器官系统的全身性血管炎。它仍然是肾脏相关疾病和死亡的重要原因。早期诊断可能很困难,对所有患者都需要高度的怀疑指数,尤其是在有不典型表现的病例中。我们报告一例GPA病例,该病例在新的和进展的症状掩盖了双侧面瘫和主动脉壁血栓的原始诊断后才被诊断出来。
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