Gangireddy Mounika, Kanderi Tejaswi, Chan Gomez Janet, Kundoor Vishwa, Cunningham Jessica
Internal Medicine, University of Pittsburgh Medical Center (UPMC) Pinnacle, Harrisburg, USA.
Internal Medicine, MedStar Franklin Square Medical Center, Baltimore, USA.
Cureus. 2020 Jun 28;12(6):e8883. doi: 10.7759/cureus.8883.
Granulomatosis with polyangiitis (GPA) is a vasculitis of small and medium-sized vessels and presents with varying signs and symptoms. It includes upper and lower airway manifestations and glomerulonephritis with a positive antineutrophil cytoplasmic antibody (ANCA) in serology in 90% of cases. However, about 10% of cases with GPA can have negative serology, often resulting in a diagnostic delay. Obtaining a tissue pathology is needed to confirm GPA. Here we present a 77-year-old male who presented with generalized weakness and loss of appetite and was found to have glomerulonephritis and bilateral opacities in the lungs with a negative ANCA. He was diagnosed with ANCA negative granulomatosis with polyangiitis after a renal biopsy revealed necrotizing inflammation with crescent formation. He was successfully treated with systemic glucocorticoids and rituximab. In conclusion, prompt diagnosis and treatment of ANCA negative vasculitis are required to decrease mortality.
肉芽肿性多血管炎(GPA)是一种中小血管的血管炎,表现出不同的体征和症状。它包括上、下呼吸道表现以及肾小球肾炎,90%的病例血清学抗中性粒细胞胞浆抗体(ANCA)呈阳性。然而,约10%的GPA病例血清学可能为阴性,常导致诊断延迟。需要进行组织病理学检查以确诊GPA。在此,我们报告一名77岁男性,他出现全身无力和食欲减退,被发现患有肾小球肾炎和双肺混浊,ANCA为阴性。肾活检显示有坏死性炎症伴新月体形成后,他被诊断为ANCA阴性肉芽肿性多血管炎。他接受全身糖皮质激素和利妥昔单抗治疗后获得成功。总之,需要对ANCA阴性血管炎进行及时诊断和治疗以降低死亡率。