• 1. Department of Pediatrics, West China Second Hospital, Sichuan University, Chengdu 610041, Sichuan, P. R. China; 2. Department of Neonatology, the Affiliated Hospital of Luzhou Medical College, Luzhou 646000, Sichuan, P. R. China.;
TAO Yuhong., Email: bzhmczhdsh@163.com
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目的  提高對先天性腹主動脈瘤(AAA)的認識。 方法  報道2012年11月1日先天性AAA 1 例,回顧國內外報道的24 例先天性AAA的臨床資料。 結果  患兒男,2歲,以肉眼血尿起病,伴高血壓、蛋白尿和反復血小板降低;多層螺旋CT血管成像(MSCTA)見AAA伴左腎動脈狹窄;彩色多普勒超聲見AAA累及雙側髂總動脈伴動脈壁間血栓及鈣化,左腎萎縮;保守治療7個月后猝死,臨終前頭顱CT見腦梗死。回顧分析24例先天性AAA,包括腎下型AAA 15 例,腎上型AAA 5例,胸腹部AAA 2例,未具體指明類型2例;產前診斷6例,出生后診斷18例(其中包括新生兒5例和1個月~3歲嬰幼兒8例);以腹部搏動性包塊起病8 例,嘔吐4 例,呼吸困難2例,腰部疼痛1例,因其他疾病就診3例;采用血管超聲21例,MSCTA 16例,磁共振血管造影9例;13例腎下型AAA接受手術治療;死于AAA破裂5例,死于心力衰竭2例。 結論  先天性AAA以腎下型為主,多為嬰幼兒,常表現為腹部腫塊,確診該病首選MSCTA,主張行早期個體化手術。

Citation: ZHANG Deshuang,WANG Yamei,CHEN Juan,TAO Yuhong.. Congenital Abdominal Aortic Aneurysm in Children: A Case Report and Literature Review. West China Medical Journal, 2013, 28(10): 1586-1589. doi: 10.7507/1002-0179.20130500 Copy

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