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先天性十二指肠膜式有孔闭锁15例临床分析 被引量:1

ONGENITAL INCOMPLETE DUODENAL DIAPHRAGMCLINICAL ANALYSIS OF 15 CASE
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摘要 1978年到1995年我院收治先天性十二指肠膜式有孔闭锁15例,男10例.女5例。年龄在2~20d10例.1~6月3例,18个月1例.2岁1例。13例经十二指肠前壁切开隔膜切除.2例十二指肠巨大扩张者作了十二指肠部分切除,结肠后十二脂肠一空场吻合术,治愈13例,死亡2例。指出新生儿婴儿十二指肠膜式有孔闭锁采用十二指肠切开隔膜切除,幼儿因十二指肠巨大扩张而采用十二指肠部份切除,十二指肠一空肠吻合术. Fifteen Patients with Congenital incomplete duodenal diaphragmwere treated between 1978 and 1995. 10 Patients were boy,5 were girl. The ages rangedfrom 2 to 20 days in 10 case. 1-6 months in 3 cases One was 18 months,Other was 2years. Incomplete diaphragm resected through duodenal incision was undergo in 13 cas-es, part duodenoctomy and duodenojejunostomy was Performed in 2 cases with giantduodenal distention, After operation, 13 Patients were cured, 2 Patients died. The aut-ther's experience Suggest that diaphragm resected through duodenal incision is a proce-dure in neonate and infant,Part duodenoctomy and duodenojejunostomy is a Procederein Young child with maedly duodenal distention.
作者 陈宗义
出处 《河北医学》 CAS 1997年第2期12-14,共3页 Hebei Medicine
关键词 十二指肠闭锁 不完全隔膜 小儿 先天性 congenital duodenal atresia incomplete diaphragm
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参考文献1

  • 1谷兴琳,陈永田.新生儿先天性十二指肠梗阻手术方法探讨[J]江苏医药,1986(08).

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