Pentalogy of Cantrell with Ectopia Cordis: CT Findings

被引：7

作者：

Pirasteh, Ali ^{[1
]}

Carcano, Carolina ^{[2
]}

Kirsch, Jacobo ^{[2
]}

Mohammed, Tan-Lucien H. ^{[3
]}

机构：

[1] Univ Texas Southwestern Med Ctr Dallas, Dept Radiol, Dallas, TX USA

[2] Cleveland Clin Florida, Dept Radiol, 2950 Cleveland Clin Blvd, Weston, FL 33331 USA

[3] Univ Florida, Coll Med, Dept Radiol, Gainesville, FL 32610 USA

来源：

JOURNAL OF RADIOLOGY CASE REPORTS | 2014年 / 8卷 / 12期

关键词：

Pentalogy of Cantrell; MDCT; Ectopia Cordis; Cardiac Malformation; Omphalocele;

D O I：

10.3941/jrcr.v8i12.1972

中图分类号：

R8 [特种医学]; R445 [影像诊断学];

学科分类号：

1002 ; 100207 ; 1009 ;

摘要：

A 14-month-old girl with pentalogy of Cantrell, a very rare congenital syndrome characterized by an epigastric omphalocele and malformations of the heart, sternum, pericardium, and diaphragm, underwent echocardiography and multidetector computed tomography before surgical repair of these deformities was attempted. These tests revealed multiple cardiovascular and noncardiovascular abnormalities. After surgery, the patient's cardiovascular status was stable. Although studies have shown that echocardiography, multidetector computed tomography, and magnetic resonance imaging may each play a role in the diagnosis and management of this condition, there are few data available to support the use of one imaging modality over another.

引用

页码：29 / 34

页数：6

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