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Bilateral silent sinus syndrome: A rare case and review of literature
OBJECTIVE: In this report, we presented a rare case of bilateral silent sinus syndrome (SSS) in an otherwise healthy 57-year-old man treated with functional endoscopic sinus surgery (FESS). A systematic review of the literature regarding bilateral SSS was performed. CASE REPORT: A 57-year-old man wi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
OceanSide Publications, Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468753/ https://www.ncbi.nlm.nih.gov/pubmed/28583234 http://dx.doi.org/10.2500/ar.2017.8.0197 |
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author | Trope, Michal Schwartz, Joseph S. Tajudeen, Bobby A. Kennedy, David W. |
author_facet | Trope, Michal Schwartz, Joseph S. Tajudeen, Bobby A. Kennedy, David W. |
author_sort | Trope, Michal |
collection | PubMed |
description | OBJECTIVE: In this report, we presented a rare case of bilateral silent sinus syndrome (SSS) in an otherwise healthy 57-year-old man treated with functional endoscopic sinus surgery (FESS). A systematic review of the literature regarding bilateral SSS was performed. CASE REPORT: A 57-year-old man with well-controlled allergic rhinitis in the absence of previous surgery or trauma presented with bilateral SSS, which was successfully managed with bilateral FESS. METHODS: A medical literature data base search of the terms “silent sinus syndrome” “maxillary atelectasis,” “imploding antrum syndrome,” and “bilateral silent sinus syndrome” was performed. The results were then narrowed to include only relevant articles. RESULTS: Relevant articles included three case reports and two articles that describe or mention bilateral SSS. Of the three case reports found, two patients presented with bilateral SSS, whereas the third patient presented metachronously, with the contralateral SSS manifesting 4 months after presentation of the initial ipsilateral SSS. CONCLUSION: The present literature regarding bilateral SSS is likely incomplete, and further investigation is required to provide greater insight into the prevalence of this disease. In this report, bilateral FESS was successful in resolving symptoms and preventing disease progression. |
format | Online Article Text |
id | pubmed-5468753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | OceanSide Publications, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54687532017-06-16 Bilateral silent sinus syndrome: A rare case and review of literature Trope, Michal Schwartz, Joseph S. Tajudeen, Bobby A. Kennedy, David W. Allergy Rhinol (Providence) Articles OBJECTIVE: In this report, we presented a rare case of bilateral silent sinus syndrome (SSS) in an otherwise healthy 57-year-old man treated with functional endoscopic sinus surgery (FESS). A systematic review of the literature regarding bilateral SSS was performed. CASE REPORT: A 57-year-old man with well-controlled allergic rhinitis in the absence of previous surgery or trauma presented with bilateral SSS, which was successfully managed with bilateral FESS. METHODS: A medical literature data base search of the terms “silent sinus syndrome” “maxillary atelectasis,” “imploding antrum syndrome,” and “bilateral silent sinus syndrome” was performed. The results were then narrowed to include only relevant articles. RESULTS: Relevant articles included three case reports and two articles that describe or mention bilateral SSS. Of the three case reports found, two patients presented with bilateral SSS, whereas the third patient presented metachronously, with the contralateral SSS manifesting 4 months after presentation of the initial ipsilateral SSS. CONCLUSION: The present literature regarding bilateral SSS is likely incomplete, and further investigation is required to provide greater insight into the prevalence of this disease. In this report, bilateral FESS was successful in resolving symptoms and preventing disease progression. OceanSide Publications, Inc. 2017-06 /pmc/articles/PMC5468753/ /pubmed/28583234 http://dx.doi.org/10.2500/ar.2017.8.0197 Text en Copyright © 2017, OceanSide Publications, Inc., U.S.A. This work is published and licensed by OceanSide Publications, Inc. The full terms of this license are available at https://www.allergyandrhinology.com/terms and incorporate the Creative Commons License Deed: (Attribution – Non-Commercial – NoDerivs 4.0 Unported (CC BY-NC-ND 4.0). By accessing the work you hereby accept the terms. Non-commercial uses of the work are permitted without any further permission from OceanSide Publications, Inc., provided the work is properly attributed. Any use of the work other then as authorized under this license or copyright law is prohibited. |
spellingShingle | Articles Trope, Michal Schwartz, Joseph S. Tajudeen, Bobby A. Kennedy, David W. Bilateral silent sinus syndrome: A rare case and review of literature |
title | Bilateral silent sinus syndrome: A rare case and review of literature |
title_full | Bilateral silent sinus syndrome: A rare case and review of literature |
title_fullStr | Bilateral silent sinus syndrome: A rare case and review of literature |
title_full_unstemmed | Bilateral silent sinus syndrome: A rare case and review of literature |
title_short | Bilateral silent sinus syndrome: A rare case and review of literature |
title_sort | bilateral silent sinus syndrome: a rare case and review of literature |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468753/ https://www.ncbi.nlm.nih.gov/pubmed/28583234 http://dx.doi.org/10.2500/ar.2017.8.0197 |
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