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Atypical Isolated Infections of the Infratemporal Fossa: A Diagnostic Challenge
INTRODUCTION: Atypical infratemporal fossa infections are rare and potentially fatal. CASE REPORT: A case of an aspergillosis localized in the infratemporal fossa and another case of tuberculosis of the infratemporal fossa originating from the maxillary sinus, is described. The first patient was imm...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639693/ https://www.ncbi.nlm.nih.gov/pubmed/26568944 |
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author | Tan, Sien Hui Chong, Aun Wee Prepageran, Narayanan |
author_facet | Tan, Sien Hui Chong, Aun Wee Prepageran, Narayanan |
author_sort | Tan, Sien Hui |
collection | PubMed |
description | INTRODUCTION: Atypical infratemporal fossa infections are rare and potentially fatal. CASE REPORT: A case of an aspergillosis localized in the infratemporal fossa and another case of tuberculosis of the infratemporal fossa originating from the maxillary sinus, is described. The first patient was immunocompromised and showed symptoms of facial numbness; whereas the other was an immunocompetent man who complained of trigeminal neuralgia type pain. It was difficult to differentiate between infection and tumour despite the utilization of computed tomography scans and magnetic resonance imaging. CONCLUSION: These cases illustrate the need for a high index of suspicion; in addition to endoscopic confirmation and histopathology to establish precise diagnosis and early intervention. |
format | Online Article Text |
id | pubmed-4639693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-46396932015-11-13 Atypical Isolated Infections of the Infratemporal Fossa: A Diagnostic Challenge Tan, Sien Hui Chong, Aun Wee Prepageran, Narayanan Iran J Otorhinolaryngol Case Report INTRODUCTION: Atypical infratemporal fossa infections are rare and potentially fatal. CASE REPORT: A case of an aspergillosis localized in the infratemporal fossa and another case of tuberculosis of the infratemporal fossa originating from the maxillary sinus, is described. The first patient was immunocompromised and showed symptoms of facial numbness; whereas the other was an immunocompetent man who complained of trigeminal neuralgia type pain. It was difficult to differentiate between infection and tumour despite the utilization of computed tomography scans and magnetic resonance imaging. CONCLUSION: These cases illustrate the need for a high index of suspicion; in addition to endoscopic confirmation and histopathology to establish precise diagnosis and early intervention. Mashhad University of Medical Sciences 2015-09 /pmc/articles/PMC4639693/ /pubmed/26568944 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Tan, Sien Hui Chong, Aun Wee Prepageran, Narayanan Atypical Isolated Infections of the Infratemporal Fossa: A Diagnostic Challenge |
title | Atypical Isolated Infections of the Infratemporal Fossa: A Diagnostic Challenge |
title_full | Atypical Isolated Infections of the Infratemporal Fossa: A Diagnostic Challenge |
title_fullStr | Atypical Isolated Infections of the Infratemporal Fossa: A Diagnostic Challenge |
title_full_unstemmed | Atypical Isolated Infections of the Infratemporal Fossa: A Diagnostic Challenge |
title_short | Atypical Isolated Infections of the Infratemporal Fossa: A Diagnostic Challenge |
title_sort | atypical isolated infections of the infratemporal fossa: a diagnostic challenge |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639693/ https://www.ncbi.nlm.nih.gov/pubmed/26568944 |
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