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A clinical review of congenital gastrointestinal anomalies
Article in Ko | WPRIM | ID: wpr-39441
Responsible library: WPRO
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.
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Full text: 1 Index: WPRIM Main subject: Anal Canal / Anus, Imperforate / Pancreas / Pyloric Stenosis / Stomach / Biliary Tract / Choledochal Cyst / Incidence / Down Syndrome / Colon Type of study: Incidence_studies / Prognostic_studies Limits: Child / Female / Humans / Infant / Male Language: Ko Journal: Journal of the Korean Pediatric Society Year: 1993 Type: Article
Full text: 1 Index: WPRIM Main subject: Anal Canal / Anus, Imperforate / Pancreas / Pyloric Stenosis / Stomach / Biliary Tract / Choledochal Cyst / Incidence / Down Syndrome / Colon Type of study: Incidence_studies / Prognostic_studies Limits: Child / Female / Humans / Infant / Male Language: Ko Journal: Journal of the Korean Pediatric Society Year: 1993 Type: Article