GERD: A debated background of achalasia

Laura Bognár *, Örs Péter Horváth, András Vereczkei
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Abstract

Achalasia is a primary esophageal motility disorder of unknown etiology, characterized by aperistalsis of the esophageal body and impaired lower esophageal sphincter (LES) relaxation. However achalasia is the best characterized esophageal motility disorder, its pathogenesis is still not entirely clarified. Available data suggest that the disease is multifactorial, involving hereditary, autoimmune and environmental factors, such as viral infections, but the exact initiating factors that may play a role in the development of the disease remain unclear. Our hypothesis is that one possible initial insult that leads to the development of achalasia can be the gastroesophageal reflux disease. This theory was first proposed by Smart et al. in 1986. In our case study we report the case of a 65-year-old woman who had typical reflux symptoms with heartburn and regurgitation for about seven years. During the year before her admission to our clinic her reflux symptoms resolved and dysphagia developed. Endoscopy revealed esophageal dilatation with erosive esophagitis, narrowed cardia and hiatal hernia. Biopsies from the distal esophagus showed chronic esophagitis and Barrett’s metaplasia. Barium swallow showed dilated esophageal body with decreased peristalsis, nonrelaxing sphincter and retention of barium. Manometry and 24-hour pH monitoring was performed. The LES pressure was 34.5 mmHg with 11.9% relaxation. 24-hour pH-metry showed acid reflux, with multiple sharp dips characteristic of typical gastroesophageal reflux, with total DeMeester score of 94.6. Using pH 3 as a discriminatory threshold for GERD the reflux score was 64.2. Achalasia and concomitant GERD was diagnosed and the patient underwent laparoscopic surgery. The hiatal hernia was reconstructed and a Heller’s myotomy with a 360 degree Nissen fundoplication was performed. At the 3-year follow-up the patient was symptom free. In summary, based on our experience and the review of the literature we believe that there is a cause-and-effect relationship between gastroesophageal reflux and the development of achalasia. We believe that the development of achalasia in patients with GERD can be a protective reaction of the esophagus against reflux. In these cases the treatment of choice should be different from that of pure achalasia patients: a laparoscopic Heller’s myotomy completed with a 360 degree Nissen fundoplication should be the recommended surgical treatment to minimize the possibility of postoperative reflux disease.

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GERD:失弛缓症的一个有争议的背景
贲门失弛缓症是一种病因不明的原发性食管运动障碍,其特征是食管体的胃蠕动和食管下括约肌(LES)松弛受损。然而贲门失弛缓症是食道运动障碍中最典型的一种,其发病机制尚不完全清楚。现有数据表明,该疾病是多因素的,涉及遗传、自身免疫和环境因素,如病毒感染,但在疾病发展中可能起作用的确切起始因素仍不清楚。我们的假设是,导致贲门失弛缓症发展的一个可能的初始损伤是胃食管反流病。该理论最早由Smart等人于1986年提出。在我们的病例研究中,我们报告了一名65岁的妇女,她有典型的反流症状,胃灼热和反流约七年。在她入院前一年,她的反流症状缓解,吞咽困难出现。内镜检查显示食管扩张伴糜烂性食管炎、贲门狭窄及裂孔疝。食管远端活检显示慢性食管炎和巴雷特化生。吞钡表现为食管体扩张,蠕动减少,括约肌不松弛,钡潴留。测压和24小时pH监测。LES压为34.5 mmHg,弛豫11.9%。24小时ph测定显示胃酸反流,呈胃食管反流特征的多次急剧下降,DeMeester总分为94.6。使用pH 3作为反流的鉴别阈值,反流评分为64.2。诊断为贲门失弛缓并伴有胃反流,患者接受腹腔镜手术。重建裂孔疝,并进行Heller肌切开术和360度Nissen底吻合。随访3年,患者无症状。总之,根据我们的经验和文献回顾,我们认为胃食管反流与贲门失弛缓症的发展之间存在因果关系。我们认为胃食管反流患者发生贲门失弛缓症可能是食道对反流的一种保护性反应。在这些情况下,治疗选择应与单纯贲门失弛缓症患者不同:腹腔镜Heller肌切开术完成360度Nissen底折叠应是推荐的手术治疗,以尽量减少术后反流疾病的可能性。
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