Fischer Edgar G, Lager Donna J
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Am J Clin Pathol. 2006 Mar;125(3):445-50. doi: 10.1309/nptp-4ukv-7ju3-elmq.
Anti-glomerular basement membrane (anti-GBM) glomerulonephritis is a rare disease caused by IgG autoantibodies against the glomerular basement membrane. We describe clinical and pathologic findings in a series of renal biopsy specimens from 80 patients. The patients ranged in age from 16 to 87 years. The age distribution was bimodal, with one peak at a young age predominated by males and a second peak in the sixth to eighth decades with females predominating. Most patients (70 [88%]) had severe necrotizing glomerulonephritis with crescents in more that 50% of glomeruli. The fraction of crescentic glomeruli in biopsy specimens correlated well with serum creatinine levels but not with serologic titers for anti-GBM antibodies. Interstitial fibrosis was uncommon and, when present, minimal to mild. Linear IgG deposition defines this entity, but immunofluorescent costaining for other immunoglobulins and complement is found frequently. To our knowledge, this is the largest series of renal biopsy specimens with anti-GBM glomerulonephritis studied to date.
抗肾小球基底膜(anti-GBM)肾小球肾炎是一种由针对肾小球基底膜的IgG自身抗体引起的罕见疾病。我们描述了80例患者的一系列肾活检标本的临床和病理表现。患者年龄在16至87岁之间。年龄分布呈双峰型,一个高峰在年轻时,以男性为主,另一个高峰在第六至第八个十年,以女性为主。大多数患者(70例[88%])患有严重的坏死性肾小球肾炎,超过50%的肾小球有新月体形成。活检标本中新月体肾小球的比例与血清肌酐水平密切相关,但与抗GBM抗体的血清学滴度无关。间质纤维化不常见,如有则为轻度至中度。线性IgG沉积可确诊该疾病,但其他免疫球蛋白和补体的免疫荧光共染色也很常见。据我们所知,这是迄今为止研究的最大系列的抗GBM肾小球肾炎肾活检标本。