All issues > Volume 33(4); 1990
- Original Article
- J Korean Pediatr Soc. 1990;33(4):456-462. Published online April 30, 1990.
- A clinicostatistical Study of Congenital Intestinal Obstruction.
- Min Young Lee1, Young Sook Hong1, Se Jin Kang1, Soon Kyum Kim1, Pyung Hwa Choe1
- 1Department of Pediatrics, College of Medicine, Korea University, Seoul, Korea
- Received: September 28, 1989; Accepted: November 6, 1989.
- Abstract
- A clinicostatistical assessment of the 134 patients with congenital intestinal obstruction who were admitted
to the department of pediatrics and pediatric surgery. Korea university medical center from Feb. 1979 to June.
1988 was performed.
The results were as follows.
1) Congenital hypertrophic pyloric stenosis (43 cases) was the' most common congenital intestinal obstruc-
tion, and congenital megacolon (24 cases), imperforate anus (23 cases), omphalocele (11 cases), diaphragmatic
hernia (9 cases), malrotation (7 cases), atresia or stenosis (6 cases), esophageal atresia with tracheoesophageal
fistula (6 cases), gastroschisis (2 cases), Meckefs diverticulum (2 cases), congenital band (1 cases) were in
order of frequency.
2) Male was predominant than female in proportioin of 2'5:1
3) Regional distribution showed that 81 cases were obstruction in large intestine and 49 cases were in small
intestine.
4) Prevalence of age was as follows; under the 6 mo of age (82.1%), 7—12 mo of age (4.5%), 2〜5 yr age
(8.3%), 6〜 10 yr of age (3.7%), over 10 yr of age (1.5%).
5) The main symptoms and signs were vomiting (53.7%), abdominal distension (29.1%), difficulty of
defecation (21.6%), dyspnea (7.5%).
6) Overall mortality rate was 5.2% (7 out of 134 cases).
Keywords :Congenital Intestinal Obstruction