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Achalasia in a Patient with Myotonic Dystrophy

Myotonic dystrophy is a progressive disorder mainly affecting the voluntary muscles. We herein report a rare case of myotonic dystrophy complicated with high-resolution manometry-defined achalasia, the pathology of which is absent relaxation of the smooth muscles of lower esophageal sphincter (LES)....

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Detalles Bibliográficos
Autores principales: Sato, Hiroki, Mizuno, Ken-ichi, Hashimoto, Satoru, Takatsuna, Masafumi, Terai, Shuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995719/
https://www.ncbi.nlm.nih.gov/pubmed/31511482
http://dx.doi.org/10.2169/internalmedicine.3360-19
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author Sato, Hiroki
Mizuno, Ken-ichi
Hashimoto, Satoru
Takatsuna, Masafumi
Terai, Shuji
author_facet Sato, Hiroki
Mizuno, Ken-ichi
Hashimoto, Satoru
Takatsuna, Masafumi
Terai, Shuji
author_sort Sato, Hiroki
collection PubMed
description Myotonic dystrophy is a progressive disorder mainly affecting the voluntary muscles. We herein report a rare case of myotonic dystrophy complicated with high-resolution manometry-defined achalasia, the pathology of which is absent relaxation of the smooth muscles of lower esophageal sphincter (LES). In the present case, achalasia was considered a complication of myotonic dystrophy instead of sporadic achalasia, as on performing high-resolution manometry, the finding of an impaired LES relaxation (myotonic phase) changed to a totally emaciated LES function (muscle weakness phase) as myotonic dystrophy progressed.
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spelling pubmed-69957192020-02-03 Achalasia in a Patient with Myotonic Dystrophy Sato, Hiroki Mizuno, Ken-ichi Hashimoto, Satoru Takatsuna, Masafumi Terai, Shuji Intern Med Case Report Myotonic dystrophy is a progressive disorder mainly affecting the voluntary muscles. We herein report a rare case of myotonic dystrophy complicated with high-resolution manometry-defined achalasia, the pathology of which is absent relaxation of the smooth muscles of lower esophageal sphincter (LES). In the present case, achalasia was considered a complication of myotonic dystrophy instead of sporadic achalasia, as on performing high-resolution manometry, the finding of an impaired LES relaxation (myotonic phase) changed to a totally emaciated LES function (muscle weakness phase) as myotonic dystrophy progressed. The Japanese Society of Internal Medicine 2019-09-11 2020-01-01 /pmc/articles/PMC6995719/ /pubmed/31511482 http://dx.doi.org/10.2169/internalmedicine.3360-19 Text en Copyright © 2020 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Sato, Hiroki
Mizuno, Ken-ichi
Hashimoto, Satoru
Takatsuna, Masafumi
Terai, Shuji
Achalasia in a Patient with Myotonic Dystrophy
title Achalasia in a Patient with Myotonic Dystrophy
title_full Achalasia in a Patient with Myotonic Dystrophy
title_fullStr Achalasia in a Patient with Myotonic Dystrophy
title_full_unstemmed Achalasia in a Patient with Myotonic Dystrophy
title_short Achalasia in a Patient with Myotonic Dystrophy
title_sort achalasia in a patient with myotonic dystrophy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995719/
https://www.ncbi.nlm.nih.gov/pubmed/31511482
http://dx.doi.org/10.2169/internalmedicine.3360-19
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