[Orphan disease of the nose and paranasal sinuses]

Laryngorhinootologie. 2015 Mar:94 Suppl 1:S272-87. doi: 10.1055/s-0034-1398514. Epub 2015 Apr 10.
[Article in German]

Abstract

Rare rhinological diseases are a diagnostic challenge. From the primary manifestation until the final diagnosis it may take several months or even up to years in which the disease progress is uncontrolled and the disease insufficiently treated. This results in (irreversible) damage and possibly life-threatening situations. The unexpected course of a (misdiagnosed) disease should lead to further diagnostic considerations and steps to detect the orphan disease at a stage as early as possible. In the present work granulomatous diseases of the nose and sinuses caused by mycobacteria, treponemes, klebsiella, fungi and protozoa as well as vasculitis, sarcoidosis, rosacea, the cocaine-induced midline destruction, the nasal extranodal NK/T-cell lymphoma and cholesterol granuloma are discussed. Furthermore diseases with disorders of mucociliary clearance as the primary ciliary dyskinesia and cystic fibrosis are presented taking into account the current literature.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Delayed Diagnosis
  • Diagnostic Errors
  • Humans
  • Nose Diseases / diagnosis*
  • Nose Diseases / etiology
  • Nose Diseases / therapy
  • Paranasal Sinus Diseases / diagnosis*
  • Paranasal Sinus Diseases / etiology
  • Paranasal Sinus Diseases / therapy
  • Rare Diseases*