Unexpected Convergence: A Case Report of Achalasia in a Patient With Multiple Sclerosis

Achalasia is an esophageal motility disorder marked by neuronal degeneration within the myenteric plexus, leading to impaired lower esophageal relaxation and swallowing dysfunction. Despite a detailed understanding of its features, the disease's cause remains unknown. Similarly, multiple sclero...

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Main Authors: Saeed S. Graham, Adrianna E. Carrasco, Jinye Liu, Mohamed Khalaf, William J. Leland
Format: Article
Language:English
Published: American College of Physicians 2025-01-01
Series:Annals of Internal Medicine: Clinical Cases
Online Access:https://www.acpjournals.org/doi/10.7326/aimcc.2024.0580
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author Saeed S. Graham
Adrianna E. Carrasco
Jinye Liu
Mohamed Khalaf
William J. Leland
author_facet Saeed S. Graham
Adrianna E. Carrasco
Jinye Liu
Mohamed Khalaf
William J. Leland
author_sort Saeed S. Graham
collection DOAJ
description Achalasia is an esophageal motility disorder marked by neuronal degeneration within the myenteric plexus, leading to impaired lower esophageal relaxation and swallowing dysfunction. Despite a detailed understanding of its features, the disease's cause remains unknown. Similarly, multiple sclerosis (MS) is an inflammatory demyelinating condition of uncertain cause. Autoimmunity has been suggested as a potential cause of both disorders, yet instances documenting their co-occurrence are rare. We report a case of achalasia diagnosed in a young woman during hospitalization for an apparent MS flare.
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publisher American College of Physicians
record_format Article
series Annals of Internal Medicine: Clinical Cases
spelling doaj-art-059ec6cb771244bba9f67cf6350c0e342025-08-20T02:11:54ZengAmerican College of PhysiciansAnnals of Internal Medicine: Clinical Cases2767-76642025-01-014110.7326/aimcc.2024.0580Unexpected Convergence: A Case Report of Achalasia in a Patient With Multiple SclerosisSaeed S. Graham0Adrianna E. Carrasco1Jinye Liu2Mohamed Khalaf3William J. Leland41Department of Internal Medicine, East Carolina University Brody School of Medicine, Greenville, North Carolina2Department of Neurology, University of California, Los Angeles, Los Angeles, California1Department of Internal Medicine, East Carolina University Brody School of Medicine, Greenville, North Carolina3Department of Gastroenterology and Hepatology, East Carolina University Brody School of Medicine, Greenville, North Carolina3Department of Gastroenterology and Hepatology, East Carolina University Brody School of Medicine, Greenville, North CarolinaAchalasia is an esophageal motility disorder marked by neuronal degeneration within the myenteric plexus, leading to impaired lower esophageal relaxation and swallowing dysfunction. Despite a detailed understanding of its features, the disease's cause remains unknown. Similarly, multiple sclerosis (MS) is an inflammatory demyelinating condition of uncertain cause. Autoimmunity has been suggested as a potential cause of both disorders, yet instances documenting their co-occurrence are rare. We report a case of achalasia diagnosed in a young woman during hospitalization for an apparent MS flare.https://www.acpjournals.org/doi/10.7326/aimcc.2024.0580
spellingShingle Saeed S. Graham
Adrianna E. Carrasco
Jinye Liu
Mohamed Khalaf
William J. Leland
Unexpected Convergence: A Case Report of Achalasia in a Patient With Multiple Sclerosis
Annals of Internal Medicine: Clinical Cases
title Unexpected Convergence: A Case Report of Achalasia in a Patient With Multiple Sclerosis
title_full Unexpected Convergence: A Case Report of Achalasia in a Patient With Multiple Sclerosis
title_fullStr Unexpected Convergence: A Case Report of Achalasia in a Patient With Multiple Sclerosis
title_full_unstemmed Unexpected Convergence: A Case Report of Achalasia in a Patient With Multiple Sclerosis
title_short Unexpected Convergence: A Case Report of Achalasia in a Patient With Multiple Sclerosis
title_sort unexpected convergence a case report of achalasia in a patient with multiple sclerosis
url https://www.acpjournals.org/doi/10.7326/aimcc.2024.0580
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