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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...

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Autores principales: Wirsching, Kornelia EC, Heinlin, Julia, Gassner, Holger G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
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.
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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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