Haddad syndrome presenting with abdominal distension associated with long-segment aganglionosis

被引：1
|
作者：
Do Chung, Woong
Lim, Gye-Yeon [1 ]
Kim, So Young [2 ]
Chung, Jae Hee
Kim, Sun Joo [2 ]
机构：
[1] Catholic Univ Korea, St Marys Hosp, Coll Med, Dept Radiol, Seoul 150713, South Korea
[2] Catholic Univ Korea, St Marys Hosp, Dept Pediat, Seoul 150713, South Korea
来源：
CLINICAL IMAGING | 2012年 / 36卷 / 02期
关键词：
Hirschsprung disease; Congenital central hypoventilation syndrome; Haddad syndrome;
D O I：
10.1016/j.clinimag.2011.08.014
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：
Haddad syndrome is a form of neurocristopathy characterized by a combination of congenital central hypoventilation syndrome and Hirschsprung disease (HD). Although Haddad syndrome is extremely rare, awareness of the combination of long-segment HD in Haddad syndrome as well as radiographic manifestations may help to ensure a timely diagnosis as well as to facilitate optimal treatment of this unusual condition. We report a case of Haddad syndrome with long-segment, intestinal aganglionosis in a newborn infant. This report emphasizes the features of HD in children with Haddad syndrome and suggests that specific attention be given to its interpretation on plain radiographs. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码：149 / 152
页数：4
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