Giant transdiaphragmatic duodenal duplication with an intraspinal neurenteric cyst as part of the split notochord syndrome: report of a case.
作者： Munechika Wakisaka , Kounosuke Nakada , Hiroaki Kitagawa , Harutugu Shimada , Shunsuke Nosaka
DOI: 10.1007/S00595-003-2732-Y
关键词:
摘要: We report the case of a 6-month-old girl with giant transdiaphragmatic duodenal duplication connecting to cervical intraspinal cyst, which compressed heart and lung, causing severe respiratory distress. removed neurenteric cyst through posterior incision at C6 C7 level, in mediastinum was right thoracotomy. Her symptoms were completely resolved by these operations.
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