Hyun J, Galen M A
Arch Intern Med. 1981 Apr;141(5):679-81. doi: 10.1001/archinte.141.5.679.
A case of acute interstitial nephritis with a distinct immunopathologic pattern was seen. The relevant findings included elevated levels of serum IgG, IgM, and IgE; persistent eosinophilia; prominent granular and electron-dense depositions of IgE and C3 in renal tubules, as demonstrated by direct immunofluorescent and electron microscopic procedures; persistent failure to demonstrate anti-basement membrane antibodies (both glomerular and tubular); and hypocomplementemia. The findings in our case suggest a type of acute interstitial nephritis with a somewhat different clinical outlook. In this respect, serial assays of complement components and IgE in serum and kidney tissue and determinations of circulating anti-basement membrane antibodies (both glomerular and tubular) may be of particular importance.
发现一例具有独特免疫病理模式的急性间质性肾炎。相关发现包括血清IgG、IgM和IgE水平升高;持续性嗜酸性粒细胞增多;直接免疫荧光和电子显微镜检查显示,肾小管中有显著的IgE和C3颗粒状及电子致密沉积物;持续未能检测到抗基底膜抗体(肾小球和肾小管);以及补体血症。我们病例中的发现提示了一种临床前景有所不同的急性间质性肾炎。在这方面,对血清和肾组织中的补体成分和IgE进行系列检测以及测定循环抗基底膜抗体(肾小球和肾小管)可能尤为重要。