| Literature DB >> 25610297 |
Berhan Genc1, Aynur Solak1, Ilhami Solak2, Mehmet Serkan Gur1.
Abstract
Achalasia is a primary esophageal motility disorder characterized by the absence of primary peristalsis and a failure of the lower esophageal sphincter to relax, resulting in a dilated esophagus. Dysphagia is the classic and most common symptom. Respiratory obstruction due to tracheal compression caused by a massively dilated esophagus is a very rare but fatal complication. Herein, we report a case of a patient with long-standing achalasia who had tracheal compression secondary to a markedly dilated, giant esophagus. These findings are documented with CT scans. His symptoms regressed after a Heller myotomy and fundoplication operation.Entities:
Keywords: Achalasia; computed tomography; dyspnea; esophageal expansion; progressive
Year: 2014 PMID: 25610297 PMCID: PMC4261440 DOI: 10.5152/eajm.2014.11
Source DB: PubMed Journal: Eurasian J Med ISSN: 1308-8734