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Orphan diseases of the nose and paranasal sinuses: Pathogenesis – clinic – therapy

Rare rhinological diseases are a diagnostic challenge. Sometimes it takes months or even years from the primary manifestation of the disease until the definitive diagnosis is establibshed. During these times the disease proceeds in an uncontrolled or insufficiently treated way. (Irreversible) damage...

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Autor principal: Laudien, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: German Medical Science GMS Publishing House 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702053/
https://www.ncbi.nlm.nih.gov/pubmed/26770278
http://dx.doi.org/10.3205/cto000119
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author Laudien, Martin
author_facet Laudien, Martin
author_sort Laudien, Martin
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description Rare rhinological diseases are a diagnostic challenge. Sometimes it takes months or even years from the primary manifestation of the disease until the definitive diagnosis is establibshed. During these times the disease proceeds in an uncontrolled or insufficiently treated way. (Irreversible) damage results and sometimes life-threatening situations occur. The unexpected course of a (misdiagnosed) disease should lead to further diagnostic reflections and steps in order to detect also rare diseases as early as possible. The present paper discusses granulomatous diseases of the nose and paranasal sinuses caused by mycobacteria, treponema, Klebsiella, fungi, and protozoa as well as vasculitis, sarcoidosis, rosacea, cocaine-induced midline destruction, nasal extranodal NK/T cell lymphoma, and cholesterol granuloma. Furthermore, diseases with disorders of the mucociliary clearance such as primary ciliary dyskinesia and cystic fibrosis are presented, taking into consideration the current literature.
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spelling pubmed-47020532016-01-14 Orphan diseases of the nose and paranasal sinuses: Pathogenesis – clinic – therapy Laudien, Martin GMS Curr Top Otorhinolaryngol Head Neck Surg Article Rare rhinological diseases are a diagnostic challenge. Sometimes it takes months or even years from the primary manifestation of the disease until the definitive diagnosis is establibshed. During these times the disease proceeds in an uncontrolled or insufficiently treated way. (Irreversible) damage results and sometimes life-threatening situations occur. The unexpected course of a (misdiagnosed) disease should lead to further diagnostic reflections and steps in order to detect also rare diseases as early as possible. The present paper discusses granulomatous diseases of the nose and paranasal sinuses caused by mycobacteria, treponema, Klebsiella, fungi, and protozoa as well as vasculitis, sarcoidosis, rosacea, cocaine-induced midline destruction, nasal extranodal NK/T cell lymphoma, and cholesterol granuloma. Furthermore, diseases with disorders of the mucociliary clearance such as primary ciliary dyskinesia and cystic fibrosis are presented, taking into consideration the current literature. German Medical Science GMS Publishing House 2015-12-22 /pmc/articles/PMC4702053/ /pubmed/26770278 http://dx.doi.org/10.3205/cto000119 Text en Copyright © 2015 Laudien http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License.
spellingShingle Article
Laudien, Martin
Orphan diseases of the nose and paranasal sinuses: Pathogenesis – clinic – therapy
title Orphan diseases of the nose and paranasal sinuses: Pathogenesis – clinic – therapy
title_full Orphan diseases of the nose and paranasal sinuses: Pathogenesis – clinic – therapy
title_fullStr Orphan diseases of the nose and paranasal sinuses: Pathogenesis – clinic – therapy
title_full_unstemmed Orphan diseases of the nose and paranasal sinuses: Pathogenesis – clinic – therapy
title_short Orphan diseases of the nose and paranasal sinuses: Pathogenesis – clinic – therapy
title_sort orphan diseases of the nose and paranasal sinuses: pathogenesis – clinic – therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702053/
https://www.ncbi.nlm.nih.gov/pubmed/26770278
http://dx.doi.org/10.3205/cto000119
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