Abstract

Achalasia, a rare primary esophageal motility disorder, is often misdiagnosed as refractory gastroesophageal reflux disease (GERD). This study is aimed to identify the clinical and histopathologic features that may help to differentiate these two entities. Patients with untreated achalasia and those with refractory reflux symptoms despite ≥8 weeks of proton-pump inhibitor treatment were enrolled prospectively. All patients underwent validated symptom questionnaires, esophagogastroduodenoscopy with biopsy, and high-resolution impedance manometry (HRIM). Histopathology of esophageal mucosa was compared based on four pre-determined histological criteria: basal cell hyperplasia or papillae elongation, eosinophilic infiltration, petechiae formation, and hypertrophy of the muscularis mucosae (MM). Compared with the GERD patients, patients with achalasia had similar reflux symptoms, but higher Eckardt scores, fewer erosive esophagitis and hiatal hernia, more esophageal food retention on endoscopy, and higher prevalence of hypertrophy of the MM and petechiae formation on histopathology. Multivariate logistic regression based on Eckardt score ≥4, normal esophagogastric junction morphology or esophageal food retention, and coexistence of petechiae formation and hypertrophy of the MM, established the best prediction model for achalasia. Therefore, combination of routinely accessible variables, including Eckardt score, endoscopic features, and histopathology obtained via esophageal mucosal biopsy, may provide an earlier identification of achalasia.

Highlights

  • Achalasia is a rare primary esophageal motility disorder involving the smooth muscle of the esophageal body and the lower esophageal sphincter (LES)

  • The diagnosis of achalasia is often delayed due to its insidious onset and the gradual progression of the disease that can occur over several years, as well as the non-specific symptoms, such as regurgitation, chest pain, and heartburn, that mimic gastroesophageal reflux disease (GERD) [7]

  • Regarding the symptom severity scores (Table 2), there was no group difference on the reflux disease questionnaire (RDQ) score, but the Eckardt score was significantly higher in achalasia patients

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Summary

Introduction

Achalasia is a rare primary esophageal motility disorder involving the smooth muscle of the esophageal body and the lower esophageal sphincter (LES). In patients with non-obstructive dysphagia, achalasia is the most common etiology [2,3]. Treatment choices for achalasia includes medical treatment, surgical myotomy, and endoscopic treatment, such as pneumatic dilatation, botulinum toxin injection, and peroral endoscopic myotomy (POEM). Without an early diagnosis and an adequate treatment, achalasia may progress to a sigmoid-type esophagus with a markedly tortuous and dilated esophageal lumen, requiring an esophagectomy and surgical reconstruction [8]. These patients have a higher risk of developing esophageal cancer, predominantly squamous cell carcinoma [9]

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