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Achalasia following gastro-oesophageal reflux.

机译:胃食管反流后的无眼症。

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摘要

Five patients initially presenting with symptomatic gastro-oesophageal reflux, proven by radiology or pH monitoring, subsequently developed achalasia, confirmed by radiology and manometry, after an interval of 2-10 years. During this period dysphagia, present as a mild and intermittent symptom accompanying the initial reflux in 3 of the 5, became severe and resulted in oesophageal stasis of food in all. Three of the 5 had a demonstrable hiatal hernia. In none was reflux a troublesome symptom after Rider-Moeller dilatation or cardiomyotomy undertaken for the achalasia. Gastro-oesophageal reflux does not protect against the subsequent development of achalasia. It is suggested that the autonomic damage eventually leading to achalasia may in its initial phases cause gastro-oesophageal reflux.
机译:5例最初表现为症状性胃食管反流的患者,经放射学或pH监测证实,随后在间隔2-10年后发展为门失弛缓症,经放射学和测压证实。在此期间,吞咽困难(伴随5例中的3例初次回流出现的轻度和间歇性症状)变得很严重,并导致食物全部食道淤积。 5例中有3例可见裂孔性疝。 Rider-Moeller扩张术或the门肌切开术治疗门失弛缓症后,均未出现反流的麻烦症状。胃食管反流不能预防随后发生的门失弛缓症。建议最终导致门失弛缓的自主神经损害可能在其初始阶段引起胃食管反流。

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