A clinical review of congenital gastrointestinal anomalies.
- Author:
Dong Hak SHIN
;
woo Hyun PARK
;
Chul Young BAE
- Publication Type:Original Article
- Keywords:
Congenital gastrointestinal anomaly
- MeSH:
Anal Canal;
Anus, Imperforate;
Biliary Tract;
Child;
Choledochal Cyst;
Colon;
Down Syndrome;
Female;
Hernia, Diaphragmatic;
Hirschsprung Disease;
Humans;
Incidence;
Infant;
Male;
Pancreas;
Parturition;
Pyloric Stenosis;
Stomach
- From:Journal of the Korean Pediatric Society
1993;36(7):944-950
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
A clinical review was done on 343 infants and children diagnosed and operated at the Department of Pediatric Surgery in Keimyung University, Dong San Medical Center for congenital gastrointestinal anomalies from January, 1988 to December, 1991. The results are summarized as follows; The most prevalent age group of congenital gastrointestinal anomaly was within first week after birth, and infants within 3months occupied 70% of total, and male to female ratio was 2:1. 2) The moat common lesion of congenital gastrointestinal anomalies was stomach with 87cases (25.4%), followed by anus with 80 cases (23.3%), colon with 63 cases (18.4%) and biliary tract with 38 cases(11.1%). 3) The most common congenital anomaly was congenital hypertophic pyloric stenosis with 87 cases (25.4%), followed by imperforate anus with 70 cases (20.4%), congenital megacolon with 63 cases (18.4%), and prevalent age was 2 week-3month, first week after birth, 1month-3year. 4) The incidence of common congenital gastrointestinal anomalies were mostly higher in male than in female but choledochal cyst was higher in female than in male. 5) Associated anomalies were observed in 14 cases (4%) of total cases, duodenal atresia was seen the highest rate of the associated anomalies and the most common associated anomaly was annular pancreas, followed by Down syndrome, congenital diaphragmatic hernia.
