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成人先天性十二指肠蹼继发十二指肠梗阻

Duodenal obstruction secondary to congenital web in an adult.

作者信息

Anderson T H, Deitel M

出版信息

Can J Surg. 1984 Jul;27(4):365-6.

PMID:6744142
Abstract

Congenital duodenal web, although rare, may be more common than presently appreciated. The possibility of this condition should be considered in the differential diagnosis of duodenal obstruction in the adult. It should be treated surgically either by duodenotomy with excision of the web or by duodenojejunostomy. The results are excellent, as illustrated by the authors in their report of a 58-year-old man with this condition, who was treated by duodenojejunostomy.

摘要

先天性十二指肠蹼虽然罕见,但可能比目前所认识到的更为常见。在成人十二指肠梗阻的鉴别诊断中应考虑到这种情况的可能性。应通过手术治疗,可采用十二指肠切开术切除蹼或十二指肠空肠吻合术。结果非常好,正如作者在报告中所述,一名患有这种疾病的58岁男性接受了十二指肠空肠吻合术治疗。

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