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Respiratory Epithelial Adenomatoid Hamartoma: A Very Rare Entity Originating from the External Auditory Canal

Respiratory epithelial adenomatoid hamartoma (REAH) is an uncommon lesion of the upper aerodigestive tract. It is characterized by abnormal glandular formations with ciliated epithelium arising from the nasal cavity, paranasal sinuses and nasopharynx, but other locations have also been described. We...

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Autores principales: Shokouhi, Behrouz, Mehrasa, Parisa, Aslani, Farzad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Society of Pathology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354067/
https://www.ncbi.nlm.nih.gov/pubmed/32754222
http://dx.doi.org/10.30699/ijp.2020.115463.2255
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author Shokouhi, Behrouz
Mehrasa, Parisa
Aslani, Farzad
author_facet Shokouhi, Behrouz
Mehrasa, Parisa
Aslani, Farzad
author_sort Shokouhi, Behrouz
collection PubMed
description Respiratory epithelial adenomatoid hamartoma (REAH) is an uncommon lesion of the upper aerodigestive tract. It is characterized by abnormal glandular formations with ciliated epithelium arising from the nasal cavity, paranasal sinuses and nasopharynx, but other locations have also been described. We did not find any other cases of this hamartomas in the external auditory canal in the literature. A 40-year-old man was referred to the otorhinolaryngology department due to otorrhea and decreased hearing from 1 year ago. Otoscopic examination showed a reddish hemorrhagic mass in the left external auditory canal. Intraoperatively, the tumor was completely resected. The pathologic findings were consistent with REAH.
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spelling pubmed-73540672020-08-03 Respiratory Epithelial Adenomatoid Hamartoma: A Very Rare Entity Originating from the External Auditory Canal Shokouhi, Behrouz Mehrasa, Parisa Aslani, Farzad Iran J Pathol Case Report Respiratory epithelial adenomatoid hamartoma (REAH) is an uncommon lesion of the upper aerodigestive tract. It is characterized by abnormal glandular formations with ciliated epithelium arising from the nasal cavity, paranasal sinuses and nasopharynx, but other locations have also been described. We did not find any other cases of this hamartomas in the external auditory canal in the literature. A 40-year-old man was referred to the otorhinolaryngology department due to otorrhea and decreased hearing from 1 year ago. Otoscopic examination showed a reddish hemorrhagic mass in the left external auditory canal. Intraoperatively, the tumor was completely resected. The pathologic findings were consistent with REAH. Iranian Society of Pathology 2020 2020-05-13 /pmc/articles/PMC7354067/ /pubmed/32754222 http://dx.doi.org/10.30699/ijp.2020.115463.2255 Text en This is an open-access article distributed under the terms of the Creative Commons Attribution-noncommercial 4.0 International License, (https://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Case Report
Shokouhi, Behrouz
Mehrasa, Parisa
Aslani, Farzad
Respiratory Epithelial Adenomatoid Hamartoma: A Very Rare Entity Originating from the External Auditory Canal
title Respiratory Epithelial Adenomatoid Hamartoma: A Very Rare Entity Originating from the External Auditory Canal
title_full Respiratory Epithelial Adenomatoid Hamartoma: A Very Rare Entity Originating from the External Auditory Canal
title_fullStr Respiratory Epithelial Adenomatoid Hamartoma: A Very Rare Entity Originating from the External Auditory Canal
title_full_unstemmed Respiratory Epithelial Adenomatoid Hamartoma: A Very Rare Entity Originating from the External Auditory Canal
title_short Respiratory Epithelial Adenomatoid Hamartoma: A Very Rare Entity Originating from the External Auditory Canal
title_sort respiratory epithelial adenomatoid hamartoma: a very rare entity originating from the external auditory canal
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354067/
https://www.ncbi.nlm.nih.gov/pubmed/32754222
http://dx.doi.org/10.30699/ijp.2020.115463.2255
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