Ulatowski Hannah, Bequest Andrea, Sharma Alisha, Jha Pinky
Internal Medicine, Medical College of Wisconsin, Milwaukee, USA.
Cureus. 2024 Jul 8;16(7):e64087. doi: 10.7759/cureus.64087. eCollection 2024 Jul.
Granulomatosis with polyangiitis (GPA) is a rare small-vessel vasculitis that typically presents with a triad of sinonasal, pulmonary, and renal symptoms. Here, we present the case of a 43-year-old female with a history of substance use disorder who presented with vision changes and worsening left eye pain over five days. Previous evaluations raised concerns about GPA versus cocaine-induced vasculitis, but diagnostic confirmation was hindered by a lack of medical follow-up. Prompt multidisciplinary intervention led to significant improvement following steroid therapy and IV antibiotics, and the patient was ultimately diagnosed with a high GPA. This case highlights the complexities involved in diagnosing and managing GPA presenting as orbital apex syndrome, particularly in patients with comorbidities and non-adherence to medical follow-up.
肉芽肿性多血管炎(GPA)是一种罕见的小血管血管炎,通常表现为鼻窦、肺部和肾脏症状三联征。在此,我们报告一例43岁有物质使用障碍病史的女性患者,她在五天内出现视力变化和左眼疼痛加重。先前的评估引发了对GPA与可卡因诱导的血管炎的担忧,但由于缺乏医学随访,诊断未能得到证实。及时的多学科干预在类固醇治疗和静脉注射抗生素后带来了显著改善,患者最终被诊断为高度活动性GPA。该病例凸显了诊断和管理表现为眶尖综合征的GPA所涉及的复杂性,特别是在伴有合并症且未坚持医学随访的患者中。