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Original Article
An 18-year experience of tracheoesophageal fistula and esophageal atresia
Juhee Seo, Do Yeon Kim, Ai Rhan Kim, Dae Yeon Kim, Seong Chul Kim, In Koo Kim, Ki Soo Kim, Chong Hyun Yoon, Soo Young Pi
Clin Exp Pediatr. 2010;53(6):705-710.   Published online June 23, 2010
Purpose

To determine the clinical manifestations and outcomes of patients with tracheoesophageal fistula (TEF) and esophageal atresia (EA) born at a single neonatal intensive care unit.

Methods

A retrospective analysis was conducted for 97 patients with confirmed TEF and EA who were admitted to the neonatal intensive care unit between 1990 and 2007.

Results

The rate of prenatal diagnosis was 12%. The average gestational age...

Case Report
A Case of the Esophageal Atresia with Proximal Tracheoesophageal Fistula
Heung Taeg Kim, Woung Jik Bae, Soon Lee Jung, Jae Won Lee
Clin Exp Pediatr. 1998;41(6):861-864.   Published online June 15, 1998
The congenital esophageal atresia with proximal tracheoesophageal fistula is a developmental defect with incomplete septation of the foregut of embryonic period and is often associated with other congenital anomaly. We experienced a case of the esophageal atresia with proximal tracheoesophageal fistula in a 1-day old male patient who was transferred from an obstetric clinic due to respiratory distress soon after birth. The baby was treated...
Original Article
Congenital Esophageal Atresia Associated with Tracheal Bronchus and Imperforate Anus.
Si Houn Hahn, Keun Haeng Cho, Young Sook Hong, Soon Kyum Kim
Clin Exp Pediatr. 1989;32(4):550-555.   Published online April 30, 1989
Esophageal atresia occurs once in 3000-4500 live births. These anomalies are thought to arise from defective differentiation of the primitive foregut into trachea and esophagus. defective growth of entodermal cells leading to atresia and an incomplete fusion of the lateral walls of the foregut to form a tracheoesophageal fistula. A full-term male baby was admitted to Guro Hospital with chief complaints of respiratory difficulty, chocking,...
A Clinical Observation on Esolhageal Atresia and Tracheoesophageal Fistula.
In Sang Jeon, Jung Hwan Choi, Jeong Kee Seo, Chong Ku Yun, Sung Chul Lee, Kwi Won Park, Woo ki Lee
Clin Exp Pediatr. 1988;31(6):691-699.   Published online June 30, 1988
To study the clinical characteristics of esophageal atresia and tracheoesophageal fistula, we carried out a retrospective review on medical records of 39 patients who were diagnosed as that by the operation, autopsy or radiolgy at the department of Pediatrics and Pediatric Surgery, Seoul National University Hospital between January 1980 and June 1987. The results were summarized as follows; 1) Type A was most common (94.8%) among...
Case Report
A Case of Combined Esophageal Atresia and Duodenal Atresia.
Ju Yeong Seo, Cheol Lee, Woo Yeong Chung, Soon Yong Lee, Yeon Soon Kim
Clin Exp Pediatr. 1985;28(9):912-915.   Published online September 30, 1985
We experienced a case of combined esophageal atresia without tracheoesophageal fistula and duodenal atresia. Choanal Atresia was also associated. The diagnosis was confirmed by prenatal ultrasonography, abdominal radiography and autopsy. A review of literatures was also presented briefly.
A Case of Esophageal Atresia with Tracheoesophageal fistula.
Ran Suh, Hye Kyung Lee, Gui Sook Choi, Hyo Jung Kim, Sung Woo Shin
Clin Exp Pediatr. 1984;27(10):1006-1010.   Published online October 31, 1984
Esophageal atresia with tracheoesophageal fistula is a rare congenital anomaly. A case of esophageal atresia with tracheoesophageal fistula in premature infant was experienced at Han II hospital. The diagnosis was suspected by difficulty in insertion of oropharyngeal tube in operating room and was confirmed by esophagogram. Fluid and antibiotics were given immediately, but the patient expired on nineth day after...
Tracheoesophageal Fistula with Esophageal Atresia.
San Ho Kim, Jong Bum Kim, Bock Keun Kee, Dae Yeal Lee
Clin Exp Pediatr. 1983;26(8):794-798.   Published online August 31, 1983
Tracheoesophageal fistula is rare congenital anomaly. A 3 days old female infant was admitted to our department of pediatrics because of mild dyspnea, vomiting and dehydration. T-E fistula was suspected by simple chest X-ray after insertion of the rubber catheter into the esophagus and confirmed by esophagogram with Dionosil. Total correction was promptly performed but 9 days later, gastrostomy was done because of leakage at the...
Original Article
A Clinicostatistical Study of Congenital Alimentary Tract Obstruction.
Sang Pok Suck, Yong Soo Youn, Han Woong Choi, Woo Ki Kim, Kwi Won Park
Clin Exp Pediatr. 1981;24(1):36-44.   Published online January 15, 1981
Clinicostatistical datsa on 314 patients with congenital alimentary tract obstruction at the Department of Pediatrics and Pediatric Surgery of Seoul National University Hospital from January, 1974 to July, 1980 are presented and reviewed. The results are as follows; 1. Congenital megacolon(133 cases) is the most common congenital alimentary tract obstruction, and anorectal malformations(127 cases), congental duodenal obstruction(20 cass), esophageal atresia(12...
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