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婴儿肥厚性幽门狭窄:综述

Infantile hypertrophic pyloric stenosis: a review.

作者信息

Spicer R D

出版信息

Br J Surg. 1982 Mar;69(3):128-35. doi: 10.1002/bjs.1800690304.

Abstract

Infantile hypertrophic pyloric stenosis is a relatively common condition and there is some recent evidence that the incidence is increasing in this country. Gastric outlet obstruction is caused by hypertrophy of the pyloric smooth muscle and the clinical presentation is with non-bilious vomiting starting at the age of 3-4 weeks. The diagnosis can usually be made by palpation of the hypertrophied pylorus. Operation has now superseded medical treatment as the treatment of choice but meticulous assessment and correction of fluid and electrolyte imbalance is essential preoperatively. The operation of pyloromyotomy as described by Ramstedt in 1912 is simple and effective, but attention to detail is necessary if minimal morbidity and zero mortality are to be achieved. Untreated, the mortality is high but, after successful treatment, these babies are healthy and normal, so that treatment is both worth while and gratifying. The aetiology is obscure; a polygenic pattern of inheritance has been shown to be a predisposing factor, but the postnatal precipitating factors are less defined. Early hopes that the hormone gastrin might prove to be the key have not been sustained by more recent research, but the role of other gastrointestinal hormones awaits clarification.

摘要

婴儿肥厚性幽门狭窄是一种相对常见的病症,最近有证据表明该国的发病率正在上升。胃出口梗阻是由幽门平滑肌肥大引起的,临床表现为3至4周龄时开始出现的非胆汁性呕吐。通常通过触诊肥大的幽门来做出诊断。手术现已取代药物治疗成为首选治疗方法,但术前细致评估并纠正液体和电解质失衡至关重要。1912年由拉姆斯泰特描述的幽门肌切开术操作简单有效,但要实现最低发病率和零死亡率,必须注重细节。若不治疗,死亡率很高,但成功治疗后,这些婴儿健康正常,因此治疗既值得又令人满意。病因不明;已表明多基因遗传模式是一个易感因素,但产后诱发因素尚不明确。早期曾希望激素胃泌素可能是关键因素,但最近的研究并未证实这一点,其他胃肠激素的作用有待阐明。

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