Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autor principal: Akhondi, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Master Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289704/
https://www.ncbi.nlm.nih.gov/pubmed/25598761
_version_ 1782352141918142464
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