Andrade Maria Margarida, Fernandes Manuel, Freire Sara, Cruz Diogo
Internal Medicine, Hospital de Cascais, Dr. José de Almeida, Cascais, PRT.
Pulmonology, Hospital de Cascais, Dr. José de Almeida, Cascais, PRT.
Cureus. 2023 Jul 13;15(7):e41826. doi: 10.7759/cureus.41826. eCollection 2023 Jul.
Granulomatosis with polyangiitis (GPA), a systemic vasculitis, is commonly characterized by the presence of antineutrophil cytoplasmic antibodies (ANCA). However, a subset of patients with limited disease may exhibit ANCA negativity. In this article, we report the case of a 40-year-old female diagnosed with GPA with intolerance to methotrexate titration and glucocorticoid therapy, leading to the initiation of rituximab treatment. Subsequently, the patient exhibited sustained clinical, laboratory, and radiological improvement. The identification of limited GPA has important therapeutic implications as the effectiveness of the medical treatment in ANCA-negative GPA may differ. Rituximab has emerged as an optimal treatment, irrespective of ANCA status, offering prolonged responses and a favorable tolerance profile in these patients.
肉芽肿性多血管炎(GPA)是一种系统性血管炎,通常以抗中性粒细胞胞浆抗体(ANCA)阳性为特征。然而,一部分局限性疾病患者可能表现为ANCA阴性。在本文中,我们报告了一例40岁女性,被诊断为GPA,对甲氨蝶呤滴定和糖皮质激素治疗不耐受,因此开始使用利妥昔单抗治疗。随后,患者在临床、实验室和影像学方面均持续改善。局限性GPA的识别具有重要的治疗意义,因为ANCA阴性GPA的药物治疗效果可能不同。无论ANCA状态如何,利妥昔单抗已成为一种最佳治疗方法,在这些患者中可提供持久的反应和良好的耐受性。