Kirkland G S, Savige J, Sinclair R A, Hennessy O
Department of Medicine, Austin Hospital, Heidelberg, Vic., Australia.
Am J Nephrol. 1996;16(5):442-5. doi: 10.1159/000169038.
Antiglomerular basement membrane (GBM) antibodies have been described previously in patients with microscopic polyarteritis but not in patients with polyarteritis nodosa alone. Where anti-GBM antibodies occur in microscopic polyarteritis, antineutrophil cytoplasm antibodies (ANCA) are usually present. We describe here a patient with polyarteritis nodosa and anti-GBM antibodies in whom ANCA could not be demonstrated. A 72-year-old woman presented with abdominal pain, diarrhoea and acute renal failure. A renal biopsy showed crescentic glomerulonephritis and linear immunofluorescence of the GBM consistent with anti-GBM disease. In addition, there was evidence of large-and medium-sized vessel vasculitis on abdominal angiography, performed because of persisting abdominal pain. There was no small vessel vasculitis on histological examination of the renal biopsy and ANCA could not be demonstrated by indirect immunofluorescence or ELISA.
抗肾小球基底膜(GBM)抗体此前已在显微镜下多血管炎患者中被描述,但单独的结节性多动脉炎患者中未发现。在显微镜下多血管炎患者出现抗GBM抗体的情况下,通常也会存在抗中性粒细胞胞浆抗体(ANCA)。我们在此描述一名患有结节性多动脉炎且存在抗GBM抗体但无法检测到ANCA的患者。一名72岁女性,出现腹痛、腹泻和急性肾衰竭。肾活检显示新月体性肾小球肾炎,GBM呈线性免疫荧光,符合抗GBM病。此外,由于持续性腹痛进行的腹部血管造影显示有大中血管血管炎。肾活检组织学检查未发现小血管血管炎,间接免疫荧光或酶联免疫吸附测定法均未检测到ANCA。