A Case of Esophageal Duplication. |
Hyung Kuk Ham1, Jeong Kyu Seoh1, Jae Seung Yang1, Baek Keun Lim1, Jong Soo Kim1, Hee Jae Joo2 |
1Department of Pediatrics, College of Medicine, Wonju Yonsei University, Wonju, Korea 2Department of Pathology, College of Medicine, Wonju Yonsei University, Wonju, Korea |
종격동의 Esophageal Duplication (식도중복) 1례 |
함형국1, 서정규1, 양재승1, 임백근1, 김종수1, 주희재2 |
1연세대학교 원주의대 소아과학교실 2연세대학교 원주의대 병리학교실 |
Received: 8 July 1989 • Accepted: 8 July 1989 |
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Abstract |
Esophageal duplication, a term used synonymously with enteric cyst, foregut cyst, gastroenteric
cyst, enteric duplication, and etc, is a rare developmental anomaly which occures during differentia-
tion of the larynx, trachea, and bronchi from the primitive foregut. They may cause dysphagia,
regurgitation, pneumonia, hemoptysis, and occasionally produce alarming airway obstruction.
We experienced a case with chief complaints of pale appearance and swallowing difficulty in 5
years old male child, who was diagnosed as iron deficiency anemia as a result of esophageal
duplication in mediastinum. After the esophageal duplication was removed by resection, above
symptoms and signs were improved.
We presented this case with a review of referential literatures. |
Key Words:
Esophageal duplication |
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