Saeki T, Imai N, Ito T, Yamazaki H, Nishi S
Department of Internal Medicine, Nagaoka Red Cross Hospital, Nagaoka, Niigata, Japan. nagaoka.jrc.or.jp
Clin Nephrol. 2009 Feb;71(2):173-8. doi: 10.5414/cnp71173.
We describe an elderly man with membranous nephropathy and lymphoplasmacytic infiltration into the renal interstitium who presented with a high serum IgG4 concentration and no organ involvement in the pancreatobiliary system. Although the patient had hypocomplementemia and was positive for antinuclear antibodies, he was negative for antibodies against Sm, SS-A, SS-B and RNP, and his anti-DNA antibody titer was not elevated. Immunohistochemistry demonstrated that the infiltrated plasma cells in the renal interstitium and glomerular capillary walls were strongly positive for IgG4. Electron microscopy showed electron-dense deposits on the glomerular basement membranes and tubular basement membranes. The present case suggests that membranous nephropathy, like tubulo-interstitial nephritis, is one of the renal features of IgG4-related systemic disease.
我们描述了一名患有膜性肾病且肾间质有淋巴浆细胞浸润的老年男性,其血清IgG4浓度升高,且无胰腺胆道系统器官受累。尽管该患者有补体血症低下且抗核抗体呈阳性,但抗Sm、抗SS - A、抗SS - B和抗RNP抗体均为阴性,且其抗DNA抗体滴度未升高。免疫组化显示,肾间质和肾小球毛细血管壁浸润的浆细胞IgG4呈强阳性。电子显微镜检查显示肾小球基底膜和肾小管基底膜有电子致密沉积物。本病例提示,膜性肾病与肾小管间质性肾炎一样,是IgG4相关系统性疾病的肾脏特征之一。