Nanduri Rahul S, Gurram Alekhya, Karnath Noah, Karnath Bernard
Department of Internal Medicine, John Sealy School of Medicine, University of Texas Medical Branch, Galveston, USA.
Cureus. 2025 Aug 26;17(8):e91020. doi: 10.7759/cureus.91020. eCollection 2025 Aug.
Achalasia is a rare swallowing disorder that occurs due to the deterioration of the inhibitory neurons that control the lower esophageal sphincter (LES). Achalasia shares many clinical characteristics and symptoms with gastroesophageal reflux disease (GERD), a common process involving reflux of stomach acid into the esophagus, causing difficulties in differentiating diagnoses for therapeutic management. We report the case of a 49-year-old male patient with a history of chronic GERD who presented with dysphagia. Despite proton pump inhibitor (PPI) therapy, the patient developed worsening dysphagia. Esophagogastroduodenoscopy (EGD) suggested a diagnosis of achalasia, later confirmed with barium esophagram and manometry. Due to worsening symptoms and concerns about surgical fitness, the patient underwent bridge Botox therapy. However, further deterioration necessitated surgical myotomy. This case highlights the importance of a full dysphagia evaluation, including barium esophagram and EGD. This case also highlights the treatment of achalasia, which may include Botox injections as bridge therapy and myotomy for complete resolution.
贲门失弛缓症是一种罕见的吞咽障碍,由于控制食管下括约肌(LES)的抑制性神经元退化而发生。贲门失弛缓症与胃食管反流病(GERD)有许多临床特征和症状,胃食管反流病是一种常见的过程,涉及胃酸反流至食管,导致治疗管理中的鉴别诊断困难。我们报告一例49岁男性患者,有慢性GERD病史,出现吞咽困难。尽管使用了质子泵抑制剂(PPI)治疗,患者的吞咽困难仍加重。食管胃十二指肠镜检查(EGD)提示贲门失弛缓症诊断,后来通过食管钡餐造影和测压得以证实。由于症状加重以及对手术适应性的担忧,患者接受了肉毒杆菌毒素桥接治疗。然而,症状进一步恶化使得必须进行手术肌切开术。该病例强调了全面吞咽困难评估的重要性,包括食管钡餐造影和EGD。该病例还强调了贲门失弛缓症的治疗,可能包括肉毒杆菌毒素注射作为桥接治疗以及肌切开术以实现完全缓解。