Thrombotic microangiopathy with ANCA-associated vasculitis in a child: a case report and review of literature

被引：0

作者：

Zhang, Rui ^{[1
]}

Zhou, Jia-Fan ^{[1
]}

Liang, Meng-Jun ^{[1
]}

Huang, Ya-Juan ^{[1
]}

Li, Ai-Hua ^{[1
]}

Su, Ning ^{[1
]}

Huang, Miao-Fang ^{[1
]}

Zhang, Qian-Hui ^{[1
]}

Jiang, Zong-Pei ^{[1
]}

机构：

[1] Sun Yat Sen Univ, Affiliated Hosp 6, Dept Nephrol, 26 Yuancun Erheng Rd, Guangzhou 510655, Guangdong, Peoples R China

来源：

INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2017年 / 10卷 / 02期

关键词：

Thrombotic mircroangiopathy; ANCA-related vasculitis; HENOCH-SCHONLEIN PURPURA; HEMOLYTIC-UREMIC SYNDROME; HYPOCOMPLEMENTEMIA; GLOMERULONEPHRITIS; OUTCOMES;

D O I：

暂无

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

We describe a case with acute renal failure, pulmonary bleeding, rashes and abdominal pain in a 9-year-old girl suffered from Thrombotic mircroangiopathy (TMA). The reason of TMA was ANCA-related vasculitis, which was seldom seen in pediatric patients. This type of patient is easily misdiagnosed as henoch-schoenlein purpura. The patient was given prednisone and mycophenolate mofetil (MMF) for the treatment of ANCA-related vasculitis. The renal function returned to normal and proteinuria decreased dramatically.

引用

页码：2255 / 2258

页数：4

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