The ultrastructure of the nasal polyps in patients with and without cystic fibrosis

D. Beju, W. D. Meek, J. C. Kramer

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Nasal polyps are commonly associated with cystic fibrosis (CF) and also with idiopathic allergies, asthma, and aspirin intolerance. The pathogenesis of nasal polyp formation is controversial. The present study investigates the ultrastructure of thirteen nasal polyps surgically removed from seven CF patients and six non-CF (NCF) patients with allergic diseases, asthma, and aspirin intolerance. All nasal polyps showed focal edema, hyperplasia, atrophy, or squamous metaplasia of the epithelium. The lamina propria was moderately populated with small blood vessels and mucous glands and showed focal accumulation of inflammatory cells. The CF nasal polyps, however, revealed several specific characteristics: 1) minimal damage to the surface epithelium, 2) presence of a mucus blanket lining the apical epithelium, 3) occasional intracytoplasmic lumens, 4) continuous and fenestrated type capillaries, 5) numerous degranulated mast cells, 6) many plasma cells, often with atypical morphology and intracisternal Russell bodies, and 7) a smaller number of eosinophils as compared to the NCF nasal polyps. The results indicate significant differences between CF and NCF nasal polyps and support the multifactorial pathways theory of nasal polyp formation.

Original languageEnglish
Pages (from-to)155-165
Number of pages11
JournalJournal of Submicroscopic Cytology and Pathology
Volume36
Issue number2
StatePublished - 1 Apr 2004
Externally publishedYes

Fingerprint

Nasal Polyps
Cystic Fibrosis
Epithelium
Aspirin
Asthma
Metaplasia
Mucus
Plasma Cells
Eosinophils
Mast Cells
Atrophy
Hyperplasia
Blood Vessels
Edema
Hypersensitivity
Mucous Membrane
Fibrosis

Keywords

  • Cystic fibrosis
  • Electron microscopy
  • Nasal polyps

Cite this

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The ultrastructure of the nasal polyps in patients with and without cystic fibrosis. / Beju, D.; Meek, W. D.; Kramer, J. C.

In: Journal of Submicroscopic Cytology and Pathology, Vol. 36, No. 2, 01.04.2004, p. 155-165.

Research output: Contribution to journalArticle

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AB - Nasal polyps are commonly associated with cystic fibrosis (CF) and also with idiopathic allergies, asthma, and aspirin intolerance. The pathogenesis of nasal polyp formation is controversial. The present study investigates the ultrastructure of thirteen nasal polyps surgically removed from seven CF patients and six non-CF (NCF) patients with allergic diseases, asthma, and aspirin intolerance. All nasal polyps showed focal edema, hyperplasia, atrophy, or squamous metaplasia of the epithelium. The lamina propria was moderately populated with small blood vessels and mucous glands and showed focal accumulation of inflammatory cells. The CF nasal polyps, however, revealed several specific characteristics: 1) minimal damage to the surface epithelium, 2) presence of a mucus blanket lining the apical epithelium, 3) occasional intracytoplasmic lumens, 4) continuous and fenestrated type capillaries, 5) numerous degranulated mast cells, 6) many plasma cells, often with atypical morphology and intracisternal Russell bodies, and 7) a smaller number of eosinophils as compared to the NCF nasal polyps. The results indicate significant differences between CF and NCF nasal polyps and support the multifactorial pathways theory of nasal polyp formation.

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