Riancho-Zarrabeitia Leyre, Peiró Callizo Enriqueta, Drake-Pérez Marta, García Montesinos Belén, Terán Nuria, Martínez-Taboada Víctor M
Acta Reumatol Port. 2019 Jul 8;44(Jul-Sep (3)):258-263.
We report the case of a 15-year old girl who presented with a non-tender right upper eyelid swelling. Magnetic resonance confirmed the presence of an enlargement of the orbicular muscle with moderate contrast enhancement. Biopsy revealed the presence of necrotizing granulomatous vasculitis. Further studies ruled out systemic involvement. Thus, she was diagnosed with isolated granulomatosis with polyangiitis (GPA). Treatment with steroids and methotrexate was started. Due to the persistence of the lesion, rituximab (RTX) was added with excellent clinical and radiological response. This is, to the best of our knowledge, the first case of isolated orbital GPA treated with RTX in a pediatric patient.
我们报告了一名15岁女孩的病例,她表现为右上眼睑无痛性肿胀。磁共振成像证实眼轮匝肌增大,有中度对比增强。活检显示存在坏死性肉芽肿性血管炎。进一步检查排除了全身受累。因此,她被诊断为孤立性肉芽肿性多血管炎(GPA)。开始使用类固醇和甲氨蝶呤进行治疗。由于病变持续存在,加用了利妥昔单抗(RTX),临床和影像学反应良好。据我们所知,这是首例在儿科患者中使用RTX治疗的孤立性眼眶GPA病例。