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15例抗中性粒细胞胞浆抗体相关性血管炎患儿的回顾性临床特征及肾脏病理分析

[Retrospective clinical features and renal pathological analysis of 15 children with anti-neutrophil cytoplasmic antibody-associated vasculitis].

作者信息

Guan Na, Yao Yong, Yang Ji-Yun, Xiao Hui-Jie, Ding Jie

机构信息

Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.

出版信息

Zhonghua Er Ke Za Zhi. 2013 Apr;51(4):283-7.

Abstract

OBJECTIVE

Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a disorder with poor prognosis. This study aimed to improve the diagnosis and treatment of ANCA associated vasculitis of children, to analyze the clinical features, pathological characteristics and the prognosis of children with ANCA-associated vasculitis.

METHOD

Fifteen children with ANCA associated vasculitis who were hospitalized from 2003 to 2012 in our hospital were included. Their data of pre-diagnosis status, clinical manifestations, renal pathology, treatment and prognosis were reviewed retrospectively.

RESULT

Of the 15 children, 11 were girls and 4 boys with a mean age of 10.7 years. Fourteen children were categorized as microscopic polyangitis. The time to diagnosis varied from 0.5 month to 40 months. Hematuria and proteinuria were revealed by urine analysis in all of them, only 6 children complained with gross hematuria or edema of oliguria. Decreased glomerular filtration rate was revealed in 13 children, 8 of whom had a creatinine clearance rate of less than 15 ml/(min·1.73 m(2)). Twelve children underwent renal biopsy, crescent formation was found in 11 children. Most of the crescents were cellular fibrous crescents or fibrous crescents. Six children were diagnosed as crescentic nephritis; the process of rapidly progressive nephritis was only observed in 2 children. Segmental glomerulosclerosis or global glomerulosclerosis were found in 10 children, 3 of them were diagnosed as sclerotic glomerulonephritis. Anemia and pulmonary injury were the most common extra renal manifestations. Other extra renal manifestations included rash, pain joint, gastrointestinal symptoms, abnormal findings of cardiac ultrasonography and headache. Eight children were treated with steroid combined with cyclophosphamide, 4 were treated with steroid and mycophenolate mofetil, 2 were treated with steroid, cyclophosphamide and mycophenolate mofetil, 3 children were treated with plasma exchange. Fourteen children were followed up for 0.5 month to 4 years. The renal function did not recover in children with creatinine clearance rate of less than 30 ml/(min·1.73 m(2)), who showed crescentic glomerulonephritis or sclerotic glomerulonephritis. The children who had creatinine clearance rate of more than 30 ml/(min·1.73 m(2))had better prognosis.

CONCLUSION

More attention should be paid to ANCA-associated vasculitis among school age girls with anemia or pulmonary diseases. The renal damage was serious in children; however, the clinical manifestations were not obvious. Children with a creatinine clearance rate of less than 30 ml/(min·1.73 m(2)) had poor prognosis. Early accurate diagnosis is very important.

摘要

目的

抗中性粒细胞胞浆抗体(ANCA)相关性血管炎是一种预后较差的疾病。本研究旨在提高儿童ANCA相关性血管炎的诊断和治疗水平,分析儿童ANCA相关性血管炎的临床特征、病理特点及预后。

方法

纳入2003年至2012年在我院住院的15例ANCA相关性血管炎患儿。回顾性分析其诊断前状态、临床表现、肾脏病理、治疗及预后资料。

结果

15例患儿中,女11例,男4例,平均年龄10.7岁。14例患儿被分类为显微镜下多血管炎。诊断时间从0.5个月至40个月不等。所有患儿尿常规均显示血尿和蛋白尿,仅6例患儿主诉肉眼血尿或少尿性水肿。13例患儿肾小球滤过率降低,其中8例肌酐清除率小于15 ml/(min·1.73 m²)。12例患儿接受了肾活检,11例发现新月体形成。大多数新月体为细胞纤维性新月体或纤维性新月体。6例患儿被诊断为新月体性肾炎;仅2例患儿观察到快速进展性肾炎过程。10例患儿发现节段性肾小球硬化或全球性肾小球硬化,其中3例被诊断为硬化性肾小球肾炎。贫血和肺部损伤是最常见的肾外表现。其他肾外表现包括皮疹、关节疼痛、胃肠道症状、心脏超声异常及头痛。8例患儿接受了糖皮质激素联合环磷酰胺治疗,4例接受了糖皮质激素和霉酚酸酯治疗,2例接受了糖皮质激素、环磷酰胺和霉酚酸酯治疗,3例患儿接受了血浆置换。14例患儿随访0.5个月至4年。肌酐清除率小于30 ml/(min·1.73 m²)且表现为新月体性肾小球肾炎或硬化性肾小球肾炎的患儿肾功能未恢复。肌酐清除率大于30 ml/(min·1.73 m²)的患儿预后较好。

结论

对于有贫血或肺部疾病的学龄期女童,应更多关注ANCA相关性血管炎。儿童肾脏损害严重,但临床表现不明显。肌酐清除率小于30 ml/(min·1.73 m²)的患儿预后较差。早期准确诊断非常重要。

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