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Dysphagia revealing diffuse idiopathic skeletal hyperostosis: report of two cases and literature review

Diffuse Idiopathic Skeletal Hyperostosis (DISH) also known as Forestier's disease, is a musculoskeletal disorder characterized by the calcification of ligaments essentially the vertebral longitudinal anterior ligament. Men are generally affected. It is often asymptomatic. The most common extra-...

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Detalles Bibliográficos
Autores principales: Ghammam, Monia, Houas, Jihene, Bellakhdher, Mouna, Abdelkefi, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620073/
https://www.ncbi.nlm.nih.gov/pubmed/31312301
http://dx.doi.org/10.11604/pamj.2019.32.189.18561
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author Ghammam, Monia
Houas, Jihene
Bellakhdher, Mouna
Abdelkefi, Mohamed
author_facet Ghammam, Monia
Houas, Jihene
Bellakhdher, Mouna
Abdelkefi, Mohamed
author_sort Ghammam, Monia
collection PubMed
description Diffuse Idiopathic Skeletal Hyperostosis (DISH) also known as Forestier's disease, is a musculoskeletal disorder characterized by the calcification of ligaments essentially the vertebral longitudinal anterior ligament. Men are generally affected. It is often asymptomatic. The most common extra-spinal clinical manifestation of this disease presents as dysphagia followed by respiratory disturbances such as dyspnea and sleep apnea. In this paper we discuss two cases where the patients have experienced progressive dysphagia. Radiological findings were compatible with DISH. The management was based on diet modification and anti-inflammatory medication.
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spelling pubmed-66200732019-07-16 Dysphagia revealing diffuse idiopathic skeletal hyperostosis: report of two cases and literature review Ghammam, Monia Houas, Jihene Bellakhdher, Mouna Abdelkefi, Mohamed Pan Afr Med J Case Report Diffuse Idiopathic Skeletal Hyperostosis (DISH) also known as Forestier's disease, is a musculoskeletal disorder characterized by the calcification of ligaments essentially the vertebral longitudinal anterior ligament. Men are generally affected. It is often asymptomatic. The most common extra-spinal clinical manifestation of this disease presents as dysphagia followed by respiratory disturbances such as dyspnea and sleep apnea. In this paper we discuss two cases where the patients have experienced progressive dysphagia. Radiological findings were compatible with DISH. The management was based on diet modification and anti-inflammatory medication. The African Field Epidemiology Network 2019-04-17 /pmc/articles/PMC6620073/ /pubmed/31312301 http://dx.doi.org/10.11604/pamj.2019.32.189.18561 Text en © Monia Ghammam et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ghammam, Monia
Houas, Jihene
Bellakhdher, Mouna
Abdelkefi, Mohamed
Dysphagia revealing diffuse idiopathic skeletal hyperostosis: report of two cases and literature review
title Dysphagia revealing diffuse idiopathic skeletal hyperostosis: report of two cases and literature review
title_full Dysphagia revealing diffuse idiopathic skeletal hyperostosis: report of two cases and literature review
title_fullStr Dysphagia revealing diffuse idiopathic skeletal hyperostosis: report of two cases and literature review
title_full_unstemmed Dysphagia revealing diffuse idiopathic skeletal hyperostosis: report of two cases and literature review
title_short Dysphagia revealing diffuse idiopathic skeletal hyperostosis: report of two cases and literature review
title_sort dysphagia revealing diffuse idiopathic skeletal hyperostosis: report of two cases and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620073/
https://www.ncbi.nlm.nih.gov/pubmed/31312301
http://dx.doi.org/10.11604/pamj.2019.32.189.18561
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