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An atypical presentation of a Respiratory Epithelial Adenomatoid Hamartoma, a case report
INTRODUCTION: Respiratory Epithelial Adenomatoid Hamartoma (REAH) is a benign disease that can resemble other malignant entities. Thus, it is essential to diagnose it accurately as the treatment approach differs, from radical surgeries in malignant cases, to a simple excision in hamartoma. We presen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6742674/ https://www.ncbi.nlm.nih.gov/pubmed/31528338 http://dx.doi.org/10.1016/j.amsu.2019.08.007 |
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author | Al-Musaileem, Nisreen Qazi, Imtiaz M. Bastaki, Jassem M. Ebrahim, Mahmoud A.K. |
author_facet | Al-Musaileem, Nisreen Qazi, Imtiaz M. Bastaki, Jassem M. Ebrahim, Mahmoud A.K. |
author_sort | Al-Musaileem, Nisreen |
collection | PubMed |
description | INTRODUCTION: Respiratory Epithelial Adenomatoid Hamartoma (REAH) is a benign disease that can resemble other malignant entities. Thus, it is essential to diagnose it accurately as the treatment approach differs, from radical surgeries in malignant cases, to a simple excision in hamartoma. We present an unusual case of bilateral REAH that was misdiagnosed, and hence it was treated aggressively. CASE REPORT: A 57-year-old male patient presented with anosmia, 2-years history of bilateral nasal obstruction, and was accompanied with a moderate headache. An impression of olfactory neuroblastoma was made after history taking physical examination, and imaging studies. The patient underwent Functional Endoscopic Sinus Surgery (FESS), excisional biopsy of the cribriform plate mass bilaterally, and superior septectomy. Histopathologic examination of the bilateral masses showed sinonasal polyposis with crypting of surface mucosa and pseudoglandular formation. A diagnosis of sinonasal polyps with REAH was established. The patient's nasal obstruction improved, with no recurrence of sinusitis ± polyposis. However, he still complains of anosmia after 2-years follow-up. CONCLUSION: Although REAH is a benign disease, it is critical to reach the correct diagnosis, in order to avoid aggressive treatment. Unfortunately, the preoperative investigations were not consistent with REAH, thus it was misdiagnosed and treated aggressively. |
format | Online Article Text |
id | pubmed-6742674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-67426742019-09-16 An atypical presentation of a Respiratory Epithelial Adenomatoid Hamartoma, a case report Al-Musaileem, Nisreen Qazi, Imtiaz M. Bastaki, Jassem M. Ebrahim, Mahmoud A.K. Ann Med Surg (Lond) Original Research INTRODUCTION: Respiratory Epithelial Adenomatoid Hamartoma (REAH) is a benign disease that can resemble other malignant entities. Thus, it is essential to diagnose it accurately as the treatment approach differs, from radical surgeries in malignant cases, to a simple excision in hamartoma. We present an unusual case of bilateral REAH that was misdiagnosed, and hence it was treated aggressively. CASE REPORT: A 57-year-old male patient presented with anosmia, 2-years history of bilateral nasal obstruction, and was accompanied with a moderate headache. An impression of olfactory neuroblastoma was made after history taking physical examination, and imaging studies. The patient underwent Functional Endoscopic Sinus Surgery (FESS), excisional biopsy of the cribriform plate mass bilaterally, and superior septectomy. Histopathologic examination of the bilateral masses showed sinonasal polyposis with crypting of surface mucosa and pseudoglandular formation. A diagnosis of sinonasal polyps with REAH was established. The patient's nasal obstruction improved, with no recurrence of sinusitis ± polyposis. However, he still complains of anosmia after 2-years follow-up. CONCLUSION: Although REAH is a benign disease, it is critical to reach the correct diagnosis, in order to avoid aggressive treatment. Unfortunately, the preoperative investigations were not consistent with REAH, thus it was misdiagnosed and treated aggressively. Elsevier 2019-09-05 /pmc/articles/PMC6742674/ /pubmed/31528338 http://dx.doi.org/10.1016/j.amsu.2019.08.007 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Research Al-Musaileem, Nisreen Qazi, Imtiaz M. Bastaki, Jassem M. Ebrahim, Mahmoud A.K. An atypical presentation of a Respiratory Epithelial Adenomatoid Hamartoma, a case report |
title | An atypical presentation of a Respiratory Epithelial Adenomatoid Hamartoma, a case report |
title_full | An atypical presentation of a Respiratory Epithelial Adenomatoid Hamartoma, a case report |
title_fullStr | An atypical presentation of a Respiratory Epithelial Adenomatoid Hamartoma, a case report |
title_full_unstemmed | An atypical presentation of a Respiratory Epithelial Adenomatoid Hamartoma, a case report |
title_short | An atypical presentation of a Respiratory Epithelial Adenomatoid Hamartoma, a case report |
title_sort | atypical presentation of a respiratory epithelial adenomatoid hamartoma, a case report |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6742674/ https://www.ncbi.nlm.nih.gov/pubmed/31528338 http://dx.doi.org/10.1016/j.amsu.2019.08.007 |
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