Analysis of Duodenal Atresia and Stenosis: 34-year Experience With 79 Cases
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- Ishida Kazuo
- Department of Pediatric Surgery, Japanese Red Cross Medical Center
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- Nakahara Saori
- Department of Pediatric Surgery, Japanese Red Cross Medical Center
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- Takeyama Eriko
- Department of Pediatric Surgery, Japanese Red Cross Medical Center
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- Kawakami Tadashi
- Department of Neonatology, Japanese Red Cross Medical Center
Bibliographic Information
- Other Title
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- 先天性十二指腸閉鎖/狭窄症79 例の検討
- センテンセイ ジュウニシチョウ ヘイサ/キョウサクショウ 79レイ ノ ケントウ
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Abstract
Purpose: Although the survival rate of infants with congenital duodenal atresia has improved, some unique problems remain unresolved. Analysis of duodenal atresia and stenosis: a 34-year experience with 79 cases. <br>Methods: We have experienced 79 (male: 34; female: 45) cases with duodenal atresia and stenosis in the past. Of these cases, 34 (42.5%) had Down’s syndrome, 39 were atresia, 25 were stenosis, 15 had annular pancreas, 2 were multiple atresia, 2 suffered from apple-peel configuration of the jejunum, 45 (57%) had associated anomalies including cardiac defect, malrotation, esophageal atresia, anal atresia sites inversus, and alveolar capillary dysplasia (ACD). <br>Results: The operation procedures included duodenoduodenostomy (62), excision of the web (6), duodenojejunostomy (7), and so on. Of the operated cases, 68 survived. The causes of death were a combination of sepsis, cardiac anomaly, ACD, and extremely low-birth weight infants. Only one patient required reoperation for anastomotic obstruction. <br>Conclusion: When we manage duodenal atresia and stenosis, we always consider not only the associated anomalies but also variations of atresia, and the anomalous biliary ductal system.
Journal
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- Journal of the Japanese Society of Pediatric Surgeons
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Journal of the Japanese Society of Pediatric Surgeons 50 (2), 201-205, 2014
The Japanese Society of Pediatric Surgeons
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Details 詳細情報について
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- CRID
- 1390282679777072896
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- NII Article ID
- 130004897695
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- NII Book ID
- AN00192281
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- ISSN
- 21874247
- 0288609X
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- NDL BIB ID
- 025481925
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- CiNii Articles
- Crossref
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- Abstract License Flag
- Disallowed