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Sloughing Esophagitis: A Not So Common Entity
BACKGROUND: Sloughing esophagitis, also known as esophagitis dissecans superficialis, is a very rare and underdiagnosed entity with unknown incidence rate. It can be associated with bullous dermatoses and medications such as central nervous system depressants and those causing esophageal injury. CAS...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Master Publishing Group
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289704/ https://www.ncbi.nlm.nih.gov/pubmed/25598761 |
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author | Akhondi, Hossein |
author_facet | Akhondi, Hossein |
author_sort | Akhondi, Hossein |
collection | PubMed |
description | BACKGROUND: Sloughing esophagitis, also known as esophagitis dissecans superficialis, is a very rare and underdiagnosed entity with unknown incidence rate. It can be associated with bullous dermatoses and medications such as central nervous system depressants and those causing esophageal injury. CASE REPORT: A 55-years-old woman was recovering from renal failure due to rhabdomyolysis when she developed dysphagia and odynophagia. Esophagogastroduodenoscopy with biopsy was performed for suspected bullous pemphigus and confirmed sloughing esophagitis. She improved with intravenous steroids. CONCLUSIONS: Sloughing Esophagitis should enter our differential diagnosis more frequently. It is mostly a benign, self-limiting process but when associated with bullous dermatoses will require steroid treatment. |
format | Online Article Text |
id | pubmed-4289704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Master Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42897042015-01-16 Sloughing Esophagitis: A Not So Common Entity Akhondi, Hossein Int J Biomed Sci Case Report BACKGROUND: Sloughing esophagitis, also known as esophagitis dissecans superficialis, is a very rare and underdiagnosed entity with unknown incidence rate. It can be associated with bullous dermatoses and medications such as central nervous system depressants and those causing esophageal injury. CASE REPORT: A 55-years-old woman was recovering from renal failure due to rhabdomyolysis when she developed dysphagia and odynophagia. Esophagogastroduodenoscopy with biopsy was performed for suspected bullous pemphigus and confirmed sloughing esophagitis. She improved with intravenous steroids. CONCLUSIONS: Sloughing Esophagitis should enter our differential diagnosis more frequently. It is mostly a benign, self-limiting process but when associated with bullous dermatoses will require steroid treatment. Master Publishing Group 2014-12 /pmc/articles/PMC4289704/ /pubmed/25598761 Text en © Hossein Akhondi. Licensee Master Publishing Group http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Case Report Akhondi, Hossein Sloughing Esophagitis: A Not So Common Entity |
title | Sloughing Esophagitis: A Not So Common Entity |
title_full | Sloughing Esophagitis: A Not So Common Entity |
title_fullStr | Sloughing Esophagitis: A Not So Common Entity |
title_full_unstemmed | Sloughing Esophagitis: A Not So Common Entity |
title_short | Sloughing Esophagitis: A Not So Common Entity |
title_sort | sloughing esophagitis: a not so common entity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289704/ https://www.ncbi.nlm.nih.gov/pubmed/25598761 |
work_keys_str_mv | AT akhondihossein sloughingesophagitisanotsocommonentity |