S4229 When Myotomy Fails: A Case of Persistent Dysphagia in a Patient With Overlapping Esophageal Motor Disorders

Introduction: Dysphagia remains a challenging clinical entity, particularly in patients with overlapping or evolving esophageal motor disorders and persistent symptoms despite therapeutic interventions. While peroral endoscopic myotomy (POEM) and Heller myotomy are effective for achalasia and certain non-achalasia motility disorders, a subset of patients experience treatment failure due to incomplete myotomy, disease progression, or anatomical distortion. This case highlights the need for comprehensive physiologic evaluation and multidisciplinary management in complex cases. Case Description/Methods: A 64-year-old woman with chronic dysphagia for over a decade presented with persistent symptoms despite extensive evaluation and intervention. Initial endoscopies were unremarkable. High-resolution manometry initially showed jackhammer esophagus, leading to medical therapy and multiple dilations without lasting relief. She underwent POEM, which failed to improve symptoms. Over 50 subsequent endoscopic dilations provided only transient benefit. Repeat manometry demonstrated achalasia with absent peristalsis and a distal esophageal “ledge.” Barium swallow confirmed aperistalsis with no mechanical obstruction. One-year post-POEM, she underwent Heller myotomy, Dor fundoplication, and gastrostomy tube placement. However, she continued to report dysphagia, with repeat imaging consistent with ongoing achalasia. Despite maximal interventions, she required scheduled dilations and is now referred for further evaluation by a specialized esophageal motility team. Discussion: This case illustrates the complexity of diagnosing and managing refractory dysphagia, especially in the context of overlapping or evolving motility disorders. Earlier use of high-resolution manometry, FLIP, and multidisciplinary review may have clarified the diagnosis and guided more targeted therapy, potentially reducing unnecessary interventions and morbidity. Repeated reassessment after major interventions is essential to determine the underlying cause of persistent symptoms—whether mechanical, functional, or related to end-stage esophageal disease. In the presented case, the extensive number of endoscopies and dilations with limited benefit suggests a need for earlier, more comprehensive physiologic assessment. Ultimately, earlier integration of advanced diagnostic tools and expert review may have prevented unnecessary procedures and improved quality of life.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001144376.37912.c8
Primary Topic
Gastroesophageal reflux and treatments
Type
article
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article

S4229 When Myotomy Fails: A Case of Persistent Dysphagia in a Patient With Overlapping Esophageal Motor Disorders

Amir Masoud, Bianca Thakkar, Rachael Hagen
The American Journal of Gastroenterology
Gastroesophageal reflux and treatments
article

S4229 When Myotomy Fails: A Case of Persistent Dysphagia in a Patient With Overlapping Esophageal Motor Disorders

Amir Masoud, Bianca Thakkar, Rachael Hagen
article en

Abstract

Introduction: Dysphagia remains a challenging clinical entity, particularly in patients with overlapping or evolving esophageal motor disorders and persistent symptoms despite therapeutic interventions. While peroral endoscopic myotomy (POEM) and Heller myotomy are effective for achalasia and certain non-achalasia motility disorders, a subset of patients experience treatment failure due to incomplete myotomy, disease progression, or anatomical distortion. This case highlights the need for comprehensive physiologic evaluation and multidisciplinary management in complex cases. Case Description/Methods: A 64-year-old woman with chronic dysphagia for over a decade presented with persistent symptoms despite extensive evaluation and intervention. Initial endoscopies were unremarkable. High-resolution manometry initially showed jackhammer esophagus, leading to medical therapy and multiple dilations without lasting relief. She underwent POEM, which failed to improve symptoms. Over 50 subsequent endoscopic dilations provided only transient benefit. Repeat manometry demonstrated achalasia with absent peristalsis and a distal esophageal “ledge.” Barium swallow confirmed aperistalsis with no mechanical obstruction. One-year post-POEM, she underwent Heller myotomy, Dor fundoplication, and gastrostomy tube placement. However, she continued to report dysphagia, with repeat imaging consistent with ongoing achalasia. Despite maximal interventions, she required scheduled dilations and is now referred for further evaluation by a specialized esophageal motility team. Discussion: This case illustrates the complexity of diagnosing and managing refractory dysphagia, especially in the context of overlapping or evolving motility disorders. Earlier use of high-resolution manometry, FLIP, and multidisciplinary review may have clarified the diagnosis and guided more targeted therapy, potentially reducing unnecessary interventions and morbidity. Repeated reassessment after major interventions is essential to determine the underlying cause of persistent symptoms—whether mechanical, functional, or related to end-stage esophageal disease. In the presented case, the extensive number of endoscopies and dilations with limited benefit suggests a need for earlier, more comprehensive physiologic assessment. Ultimately, earlier integration of advanced diagnostic tools and expert review may have prevented unnecessary procedures and improved quality of life.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 53%
Gastroesophageal reflux and treatments
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