Bigler S A, Parry W M, Fitzwater D S, Baliga R
Department of Pathology, University of Mississippi Medical Center, Jackson 39216-4505, USA.
Am J Kidney Dis. 1997 Nov;30(5):710-2. doi: 10.1016/s0272-6386(97)90497-2.
Anti-glomerular basement membrane antibody disease is an autoimmune disease that has rarely been described in children, and no cases have previously been described in a patient younger than 2.5 years of age. We report an 11-month-old infant girl who developed anti-glomerular basement membrane disease and progressed to end-stage renal disease and eventual renal transplantation. Although it has been suggested that this disease does not occur in infants, the possibility of anti-glomerular basement membrane disease must be considered in the differential diagnosis of acute renal failure and glomerulonephritis in an infant. The characteristic linear pattern of immunofluorescent studies for Immunoglobulin (Ig) G is important in suggesting the diagnosis, which can be confirmed by serologic testing for antibody titers.
抗肾小球基底膜抗体病是一种在儿童中很少被描述的自身免疫性疾病,此前在2.5岁以下的患者中尚未有病例报道。我们报告了一名11个月大的女婴,她患上了抗肾小球基底膜病,并进展为终末期肾病,最终接受了肾移植。尽管有人认为这种疾病不会在婴儿中发生,但在婴儿急性肾衰竭和肾小球肾炎的鉴别诊断中,必须考虑抗肾小球基底膜病的可能性。免疫球蛋白(Ig)G免疫荧光研究的特征性线性模式对提示诊断很重要,这可以通过抗体滴度的血清学检测来确诊。