書誌事項
- タイトル別名
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- Congenital Pyloric Atresia in Siblings : A Case Report and the Review of the literature
- ドウホウ ニ ハッショウシタ センテンセイ ユウモン ヘイサショウ
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抄録
Congenital pyloric atresia is extremely rare. We have experienced the disease occurred in siblings (older and younger brothers). This paper reports a younger case of congenital pyloric atresia complicated with epidermolysis bullosa and the review of the literature concerning the familiar occurrence. A baby boy, antenately diagnosed as pyloric atresia by ultrasonography was delivered normally with 33 weeks gestation, weighning 2,450 gr. Since 26th week of pregnancy, hydramnios was noted. He was admitted to our department just after birth. Abdominal plain X-p showed single bubble sign. At on day of age, a laparotomy was performed. Pyloric atresia due to the cord structure was found and the resection of the pylorus with end-to-end gastroduodenostomy was performed. His postoperative course was uneventful, but mild epidermolysis bullosa was found in this case postoperatively. The investigation of HLA typing, and the pedigree will be needed to clarify the hereditary transmission, as the high incidence of familiar occurrence was noted.
収録刊行物
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- Journal of the Japanese Society of Pediatric Surgeons
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Journal of the Japanese Society of Pediatric Surgeons 19 (6), 1053-1059, 1983
特定非営利活動法人 日本小児外科学会
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詳細情報 詳細情報について
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- CRID
- 1390001204805596800
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- NII論文ID
- 110002096207
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- NII書誌ID
- AN00192281
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- ISSN
- 21874247
- 0288609X
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- NDL書誌ID
- 2642687
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- 本文言語コード
- ja
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- データソース種別
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- JaLC
- NDL
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可