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Case report of robotic dor fundoplication for scleroderma esophagus with aperistalsis on manometry

Scleroderma is a systemic disease of collagen deposition resulting in fibrosis of small arteries and arterioles. It commonly affects the skin, lungs, and gastrointestinal tract. The most common site of GI tract involvement is the esophagus. We present the case report of a 44 year old female with scl...

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Autores principales: Andrade, Alonso, Folstein, Matthew K., Davis, Brian R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480277/
https://www.ncbi.nlm.nih.gov/pubmed/28645009
http://dx.doi.org/10.1016/j.ijscr.2017.06.020
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author Andrade, Alonso
Folstein, Matthew K.
Davis, Brian R.
author_facet Andrade, Alonso
Folstein, Matthew K.
Davis, Brian R.
author_sort Andrade, Alonso
collection PubMed
description Scleroderma is a systemic disease of collagen deposition resulting in fibrosis of small arteries and arterioles. It commonly affects the skin, lungs, and gastrointestinal tract. The most common site of GI tract involvement is the esophagus. We present the case report of a 44 year old female with scleroderma esophagus and severe reflux which was successfully treated with robotic dor fundoplication. Because of the wide variety of symptoms with which this problem can present, a tailored approach taking into consideration the patient’s symptomatology and findings during diagnostic work-up was implemented with good results. The patient exhibited complete resolution of symptoms at short term follow up. Robotic dor fundoplication is an effective option for patients with scleroderma esophagus and no evidence of hiatal hernia or esophageal shortening.
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spelling pubmed-54802772017-06-29 Case report of robotic dor fundoplication for scleroderma esophagus with aperistalsis on manometry Andrade, Alonso Folstein, Matthew K. Davis, Brian R. Int J Surg Case Rep Case Report Scleroderma is a systemic disease of collagen deposition resulting in fibrosis of small arteries and arterioles. It commonly affects the skin, lungs, and gastrointestinal tract. The most common site of GI tract involvement is the esophagus. We present the case report of a 44 year old female with scleroderma esophagus and severe reflux which was successfully treated with robotic dor fundoplication. Because of the wide variety of symptoms with which this problem can present, a tailored approach taking into consideration the patient’s symptomatology and findings during diagnostic work-up was implemented with good results. The patient exhibited complete resolution of symptoms at short term follow up. Robotic dor fundoplication is an effective option for patients with scleroderma esophagus and no evidence of hiatal hernia or esophageal shortening. Elsevier 2017-06-16 /pmc/articles/PMC5480277/ /pubmed/28645009 http://dx.doi.org/10.1016/j.ijscr.2017.06.020 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Andrade, Alonso
Folstein, Matthew K.
Davis, Brian R.
Case report of robotic dor fundoplication for scleroderma esophagus with aperistalsis on manometry
title Case report of robotic dor fundoplication for scleroderma esophagus with aperistalsis on manometry
title_full Case report of robotic dor fundoplication for scleroderma esophagus with aperistalsis on manometry
title_fullStr Case report of robotic dor fundoplication for scleroderma esophagus with aperistalsis on manometry
title_full_unstemmed Case report of robotic dor fundoplication for scleroderma esophagus with aperistalsis on manometry
title_short Case report of robotic dor fundoplication for scleroderma esophagus with aperistalsis on manometry
title_sort case report of robotic dor fundoplication for scleroderma esophagus with aperistalsis on manometry
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480277/
https://www.ncbi.nlm.nih.gov/pubmed/28645009
http://dx.doi.org/10.1016/j.ijscr.2017.06.020
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