IV型回盲瓣闭锁致新生儿回肠穿孔

Tuğba Acer Demir, E. Arslan
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引用次数: 2

摘要

在先天性肠闭锁患者中的应用。结肠闭锁仅占肠道闭锁的1.8-5%,据报道每6.6万新生儿中有1例。1、2结肠闭锁的死亡率为25.7%,随着治疗的延迟而增加结肠闭锁多见于右结肠与其他肠闭锁一样,结肠闭锁可分为:I型,膜性闭锁,肠壁连续;II型,被纤维索隔开的盲尾肠(肠壁不连续,肠系膜完整);III型:盲尾肠,两端肠系膜缺损;IV型,多发闭锁结肠闭锁以III型居多(60.4%)。在所有结肠闭锁中,I型(膜性)闭锁占15%,IV型(多发性)闭锁占10%
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Neonatal Ileal Perforation due to Type IV Ileocecal Valve Atresia
ing in patients with congenital intestinal atresia. Colonic atresia accounts for only 1.8-5% of intestinal atresia with the reported incidence of 1 in 66 000 births.1,2 Mortality rate of colonic atresia, which increases with delayed treatment, is 25.7%.3 Colonic atresia is mostly located in the right colon.3 Like other intestinal atresia colonic atresia is classified as: Type I, membranous atresia with continuous intestinal wall; Type II, blind ending intestines separated by fibrous cord (no continuous intestinal wall but intact mesentery); Type III, blind ending intestines with mesenteric defect between two ends; Type IV, multiple atresias.4 Most of the colonic atresia is type III (60.4%). The rate of type I (membranous) atresia is 15% and type IV (multiple) atresia is 10% among all colonic atresia.3
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