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Netherton syndrome - Why ENT surgeons should be aware of this rare disease - report of a case
BACKGROUND: Comèl-Netherton syndrome is an inherited ichthyosis that is associated with highly impaired epidermal cornification and barrier function. Literature sparsely reports of the occurrence of early onset skin cancer in people with Netherton syndrome. To the best of our knowledge the suitabili...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707821/ https://www.ncbi.nlm.nih.gov/pubmed/23829563 http://dx.doi.org/10.1186/1472-6815-13-7 |
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author | Wirsching, Kornelia EC Heinlin, Julia Gassner, Holger G |
author_facet | Wirsching, Kornelia EC Heinlin, Julia Gassner, Holger G |
author_sort | Wirsching, Kornelia EC |
collection | PubMed |
description | BACKGROUND: Comèl-Netherton syndrome is an inherited ichthyosis that is associated with highly impaired epidermal cornification and barrier function. Literature sparsely reports of the occurrence of early onset skin cancer in people with Netherton syndrome. To the best of our knowledge the suitability of the severely altered skin in patients with Netherton syndrome for techniques of facial plastic reconstructive surgery has not been discussed in literature yet. CASE PRESENTATION: We present a 31-year-old caucasian female patient with Netherton syndrome who developed a defect of the right nasal ala. Biopsy revealed a well differentiated squamous cell carcinoma. We describe the reconstruction of a full thickness nasal defect with a paramedian forehead flap and an epidermal turn-in flap in Netherton syndrome. Despite the altered skin texture, reconstruction and healing were uneventful and the surgical result was favourable. CONCLUSION: Therefore the authors state that the development of cutaneous malignancies should be included as a possible complication in patients with Netherton syndrome. Standard techniques of surgical facial reconstruction can be applied in these patients; healing and outcome do not appear to be negatively affected by the underlying disease. |
format | Online Article Text |
id | pubmed-3707821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37078212013-07-11 Netherton syndrome - Why ENT surgeons should be aware of this rare disease - report of a case Wirsching, Kornelia EC Heinlin, Julia Gassner, Holger G BMC Ear Nose Throat Disord Case Report BACKGROUND: Comèl-Netherton syndrome is an inherited ichthyosis that is associated with highly impaired epidermal cornification and barrier function. Literature sparsely reports of the occurrence of early onset skin cancer in people with Netherton syndrome. To the best of our knowledge the suitability of the severely altered skin in patients with Netherton syndrome for techniques of facial plastic reconstructive surgery has not been discussed in literature yet. CASE PRESENTATION: We present a 31-year-old caucasian female patient with Netherton syndrome who developed a defect of the right nasal ala. Biopsy revealed a well differentiated squamous cell carcinoma. We describe the reconstruction of a full thickness nasal defect with a paramedian forehead flap and an epidermal turn-in flap in Netherton syndrome. Despite the altered skin texture, reconstruction and healing were uneventful and the surgical result was favourable. CONCLUSION: Therefore the authors state that the development of cutaneous malignancies should be included as a possible complication in patients with Netherton syndrome. Standard techniques of surgical facial reconstruction can be applied in these patients; healing and outcome do not appear to be negatively affected by the underlying disease. BioMed Central 2013-07-06 /pmc/articles/PMC3707821/ /pubmed/23829563 http://dx.doi.org/10.1186/1472-6815-13-7 Text en Copyright © 2013 Wirsching et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Wirsching, Kornelia EC Heinlin, Julia Gassner, Holger G Netherton syndrome - Why ENT surgeons should be aware of this rare disease - report of a case |
title | Netherton syndrome - Why ENT surgeons should be aware of this rare disease - report of a case |
title_full | Netherton syndrome - Why ENT surgeons should be aware of this rare disease - report of a case |
title_fullStr | Netherton syndrome - Why ENT surgeons should be aware of this rare disease - report of a case |
title_full_unstemmed | Netherton syndrome - Why ENT surgeons should be aware of this rare disease - report of a case |
title_short | Netherton syndrome - Why ENT surgeons should be aware of this rare disease - report of a case |
title_sort | netherton syndrome - why ent surgeons should be aware of this rare disease - report of a case |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707821/ https://www.ncbi.nlm.nih.gov/pubmed/23829563 http://dx.doi.org/10.1186/1472-6815-13-7 |
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