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Adult-Onset Woakes' Syndrome: Report of a Rare Case

Introduction. Woakes' syndrome, commonly defined as severe recurrent nasal polyps with consecutive destruction of the nasal pyramid, is rare with only a few reports in the literature documenting surgical treatment of the external nose. Case Presentation. We describe the case of an adult patient...

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Autores principales: Schoenenberger, U., Tasman, A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377376/
https://www.ncbi.nlm.nih.gov/pubmed/25861503
http://dx.doi.org/10.1155/2015/857675
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author Schoenenberger, U.
Tasman, A. J.
author_facet Schoenenberger, U.
Tasman, A. J.
author_sort Schoenenberger, U.
collection PubMed
description Introduction. Woakes' syndrome, commonly defined as severe recurrent nasal polyps with consecutive destruction of the nasal pyramid, is rare with only a few reports in the literature documenting surgical treatment of the external nose. Case Presentation. We describe the case of an adult patient with Samter's triad who had been surgically treated from nasal polyposis since 2002. By 2014 a conspicuous deformity of the nasal pyramid had progressively occurred due to a recurrence. The patient underwent revision endoscopic sinus surgery and narrowing of the bony nasal vault by digital compression without osteotomies. Discussion. Having been described over 130 years ago, the etiology of Woakes' syndrome remains poorly understood. Treatment includes endoscopic sinus surgery and topical treatment. Surgical treatment of the external nose deformity by rhinoplasty is rarely addressed. Conclusion. This case illustrates that the widening of the bony nasal vault may be successfully corrected by digital compression, if the nasal bones are substantially thinned, in combination with surgical treatment of nasal polyps.
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spelling pubmed-43773762015-04-08 Adult-Onset Woakes' Syndrome: Report of a Rare Case Schoenenberger, U. Tasman, A. J. Case Rep Otolaryngol Case Report Introduction. Woakes' syndrome, commonly defined as severe recurrent nasal polyps with consecutive destruction of the nasal pyramid, is rare with only a few reports in the literature documenting surgical treatment of the external nose. Case Presentation. We describe the case of an adult patient with Samter's triad who had been surgically treated from nasal polyposis since 2002. By 2014 a conspicuous deformity of the nasal pyramid had progressively occurred due to a recurrence. The patient underwent revision endoscopic sinus surgery and narrowing of the bony nasal vault by digital compression without osteotomies. Discussion. Having been described over 130 years ago, the etiology of Woakes' syndrome remains poorly understood. Treatment includes endoscopic sinus surgery and topical treatment. Surgical treatment of the external nose deformity by rhinoplasty is rarely addressed. Conclusion. This case illustrates that the widening of the bony nasal vault may be successfully corrected by digital compression, if the nasal bones are substantially thinned, in combination with surgical treatment of nasal polyps. Hindawi Publishing Corporation 2015 2015-03-10 /pmc/articles/PMC4377376/ /pubmed/25861503 http://dx.doi.org/10.1155/2015/857675 Text en Copyright © 2015 U. Schoenenberger and A. J. Tasman. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Schoenenberger, U.
Tasman, A. J.
Adult-Onset Woakes' Syndrome: Report of a Rare Case
title Adult-Onset Woakes' Syndrome: Report of a Rare Case
title_full Adult-Onset Woakes' Syndrome: Report of a Rare Case
title_fullStr Adult-Onset Woakes' Syndrome: Report of a Rare Case
title_full_unstemmed Adult-Onset Woakes' Syndrome: Report of a Rare Case
title_short Adult-Onset Woakes' Syndrome: Report of a Rare Case
title_sort adult-onset woakes' syndrome: report of a rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377376/
https://www.ncbi.nlm.nih.gov/pubmed/25861503
http://dx.doi.org/10.1155/2015/857675
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