Journal of Internal Medicine Concepts & Practice ›› 2025, Vol. 20 ›› Issue (05): 410-414.doi: 10.16138/j.1673-6087.2025.05.12
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Received:2024-11-20
Online:2025-12-10
Published:2025-12-26
Contact:
LI Huilin
E-mail:medlhl@163.com
CLC Number:
ZHANG Xiaoyan, LI Huilin. Renal manifestations of rheumatic autoimmune diseases[J]. Journal of Internal Medicine Concepts & Practice, 2025, 20(05): 410-414.
Table 1
Renal involvement in systemic vasculitis
| 疾病类型 | 肾受累率 | 临床表现 | 病理表现 | ANCA阳性 |
| MPO:髓过氧化物酶(myeloperoxidase);p-ANCA:核周型ANCA(perinuclear ANCA);PR3-ANCA: 蛋白酶3ANCA(proteinase 3 ANCA) | ||||
| MPA | 80% | 急进性肾小球肾炎、无症状性血尿、不同程度蛋白尿及肾功能不全 | 寡免疫复合物沉积、轻度局灶节段性肾小球肾炎、弥漫坏死性新月体性肾小球肾炎、间质性肾炎 | 60%~80%,主要为MPO-ANCA及p-ANCA阳性 |
| GPA | 60%~80% | 急进性肾小球肾炎、无症状性血尿、不同程度蛋白尿及肾功能不全 | 寡免疫复合物沉积、轻度局灶节段性肾小球肾炎、弥漫坏死性新月体性肾小球肾炎,偶见肉芽肿 | 70%~90%为PR3-ANCA阳性,少数为MPO-ANCA阳性 |
| EGPA | 20% | 急进性肾小球肾炎、无症状性血尿、不同程度蛋白尿及肾功能不全 | 坏死性新月体性肾小球肾炎、嗜酸性粒细胞性间质性肾炎、膜性肾小球肾炎、局灶节段性肾小球硬化 | 1/3患者ANCA阳性,多为p-ANCA |
| 大动脉炎 | 78.1% | 高血压、蛋白尿、肾功能不全、ESKD | 肾动脉狭窄 | / |
| 结节性多动脉炎 | 不详 | 急进性肾衰竭,镜下血尿甚至肉眼血尿、细胞管型、蛋白尿、肾性高血压、肾病综合征 | 缺血性肾病、肾微动脉瘤、输尿管周围组织血管炎及继发纤维化 | / |
Table 2
Renal involvement in other rheumatic diseases
| 肾受累率 | 临床表现 | 病理表现 | 鉴别诊断 | |
| SSc | 35%~40%[ | 50%的SSc患者表现为轻度蛋白尿、血肌酐升高和(或)高血压, 6%发生硬皮病肾危象[ | 血管腔狭窄堵塞的内膜增殖和增厚,伴向心性“葱皮样”肥大、血栓性微血管病 | 其他原因所致的肾功能不全、硬皮病肾危象需要与其他血栓性微血管病相鉴别 |
| MCTD | 25%[ | 肾小球肾炎、肾病综合征、肾小管酸中毒、肾脏浓缩功能受损、肾结石或间质性肾炎[ | 膜性肾病、TIN、系膜增生性肾小球肾炎 | 原发性膜性肾病、其他原因引起的肾小管及肾间质炎 |
| IgG4-RD | 7.0%~24.6%[ | 肾功能不全、尿检异常、尿路梗阻、肾盂占位 | TIN、膜性肾病 | 药物性间质性肾炎、慢性肾盂肾炎、多中心型淋巴结增生症、其他自身免疫性疾病相关间质性肾炎 |
| AS | 10%~35%[ | 尿检异常 | 非特异性肾小球病、IgA肾病、淀粉样变性 | 与原发性肾小球病较难鉴别,需从临床表现、全面体检、辅助检查等鉴别 |
| RA | 很少直接导致 | 尿检异常 | 系膜增生性或膜性肾小球肾炎、淀粉样变性 | 与原发性肾小球病及药物引起的肾损伤相鉴别,控制RA可改善淀粉样变 |
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