Ohashi Naro, Namikawa Akio, Ono Masafumi, Iwakura Takamasa, Isobe Shinsuke, Tsuji Takayuki, Kato Akihiko, Yasuda Hideo
Internal Medicine 1, Hamamatsu University School of Medicine, Japan.
Blood Purification Unit, Hamamatsu University School of Medicine, Japan.
Intern Med. 2017 Oct 1;56(19):2617-2621. doi: 10.2169/internalmedicine.8757-16. Epub 2017 Sep 6.
A 55-year-old woman presented with deafness, increased levels of myeloperoxidase (MPO)-antineutrophil cytoplasmic antibody (ANCA), and renal insufficiency with proteinuria and hematuria. Renal biopsy revealed crescentic glomerulonephritis with the linear deposition of immunoglobulin G along the glomerular basement membrane (GBM) and peritubular capillaritis. The anti-GBM antibody levels on admission and 10 days after admission were 11.7 U/mL and 127 U/mL, respectively. These results indicated the sequential development of anti-GBM nephritis and MPO-ANCA-associated vasculitis. This report shows that anti-GBM nephritis may be caused by MPO-ANCA-associated vasculitis because of preceding otitis media, the sequential anti-GBM antibody titers, and the findings of peritubular capillaritis.
一名55岁女性出现耳聋、髓过氧化物酶(MPO)-抗中性粒细胞胞浆抗体(ANCA)水平升高以及伴有蛋白尿和血尿的肾功能不全。肾活检显示为新月体性肾小球肾炎,免疫球蛋白G沿肾小球基底膜(GBM)呈线性沉积以及肾小管周围毛细血管炎。入院时及入院10天后抗GBM抗体水平分别为11.7 U/mL和127 U/mL。这些结果表明抗GBM肾炎和MPO-ANCA相关性血管炎呈序贯性发展。本报告显示,由于先前存在中耳炎、抗GBM抗体滴度呈序贯性变化以及肾小管周围毛细血管炎的表现,抗GBM肾炎可能由MPO-ANCA相关性血管炎引起。