Rahima Kenan, Hijazi Mohamad, Kutaiba Albuni Mhd, Taheri Sogand, Muddana Venkata
Trihealth Good Samaritan Hospital, Cincinnati, OH.
UHS Southwest Healthcare, Palmdale Regional Medical Center, Palmdale, CA.
ACG Case Rep J. 2025 May 16;12(5):e01709. doi: 10.14309/crj.0000000000001709. eCollection 2025 May.
The concomitant presence of esophageal achalasia and esophagogastric junction submucosal leiomyoma is extremely rare. Peroral endoscopic myotomy has been endorsed as one of the primary interventions to manage esophageal achalasia. We present a 49-year-old woman who had initial endoscopic evaluation and diagnosis of achalasia type II then underwent peroral endoscopic myotomy and found to have incidental submucosal leiomyoma at 1 cm distal to esophagogastric junction. It was removed successfully by submucosal tunneling endoscopic resection. This poses the question of whether this is a case of achalasia or pseudoachalasia caused by leiomyoma.
食管贲门失弛缓症与食管胃交界黏膜下平滑肌瘤同时存在极为罕见。经口内镜下肌切开术已被认可为治疗食管贲门失弛缓症的主要干预措施之一。我们报告一名49岁女性,最初经内镜评估诊断为Ⅱ型失弛缓症,随后接受经口内镜下肌切开术,结果发现在食管胃交界远端1 cm处有偶然发现的黏膜下平滑肌瘤。通过黏膜下隧道内镜切除术成功将其切除。这就引发了一个问题,即这是一例由平滑肌瘤引起的失弛缓症还是假性失弛缓症。