Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, 4 rue Larrey, 49033 Angers CEDEX 09, Angers, France.
LUNAM Université, Angers, France.
BMC Nephrol. 2019 Aug 27;20(1):334. doi: 10.1186/s12882-019-1531-7.
The value of ANCA positivity in the setting of systemic lupus erythematous and their pathogenicity remains uncertain.
We report the case of a 48-year-old female with rapidly progressive kidney failure, arthro-myalgia and weight loss. Auto-immune screening showed anti-dsDNA antibodies, complement consumption and triple ANCA positivity. A first kidney biopsy done at presentation highlighted class IV-G glomerulonephritis with elective extra-capillary involvement and mainly C1q glomerular deposition at immunofluorescence study. After three months of a regimen combining steroids and cyclophosphamide, a second biopsy was performed and showed class IV-G glomerulonephritis with mainly endocapillary proliferation.
This case is atypical in view of immunological profile and kidney histopathological presentation and evolution and gives rise to discussion in view of recent data on ANCA value in lupus nephritis, and suggests that different auto-immune pathways may be involved in lupus nephritis.
在系统性红斑狼疮的背景下,抗中性粒细胞胞浆抗体(ANCA)的阳性价值及其致病性仍不确定。
我们报告了一例 48 岁女性病例,其表现为快速进展性肾衰竭、关节痛和体重减轻。自身免疫筛查显示抗双链 DNA 抗体、补体消耗和三联 ANCA 阳性。在初次就诊时进行的首次肾活检显示,免疫荧光研究显示,免疫球蛋白 G 类 IV 型肾小球肾炎伴选择性细胞外毛细血管受累,主要为 C1q 肾小球沉积。在接受类固醇和环磷酰胺联合治疗三个月后,进行了第二次活检,结果显示为免疫球蛋白 G 类 IV 型肾小球肾炎,主要为内皮细胞内增生。
鉴于免疫组化和肾脏组织病理学表现和演变,该病例不典型,并且鉴于狼疮性肾炎中抗中性粒细胞胞浆抗体的价值的最新数据,引发了讨论,提示不同的自身免疫途径可能参与狼疮性肾炎。