TextbookENTNasal Polyps

Nasal Polyps

Nasal polyps are benign, pedunculated, oedematous mucosal outgrowths arising from the paranasal sinuses, associated with chronic rhinosinusitis, asthma, and aspirin sensitivity, managed with intranasal corticosteroids and surgery when refractory.

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Key Facts

Nasal polyps affect 1-4% of the general population; more common in males and those >40 years Strongly associated with asthma (20-50% of polyp patients), aspirin-exacerbated respiratory disease (Samter's triad), and cystic fibrosis Arise from ethmoid sinus mucosa in most cases; appear as pale, grey, glistening, insensitive masses Unilateral nasal polyp in an adult must be biopsied to exclude malignancy (inverted papilloma, SCC) Intranasal corticosteroid drops (betamethasone 0.1%, fluticasone, mometasone) are first-line medical treatment Short course oral prednisolone (25-30mg OD for 5-10 days) for significant polyps or pre-operatively FESS with polypectomy for polyps refractory to maximal medical therapy Dupilumab (anti-IL4/13 monoclonal antibody) is approved for severe CRSwNP refractory to steroids and surgery (NICE TA851)

Overview

Key Facts

Nasal polyps are benign inflammatory growths of the nasal and paranasal sinus mucosa. They are a common manifestation of chronic rhinosinusitis and are associated with asthma, aspirin sensitivity, and cystic fibrosis. They cause nasal obstruction and anosmia and often require combined medical and surgical management.

Epidemiology

  • Prevalence: 1-4% of the general population
  • Male:female ratio 2:1
  • Peak onset: >40 years; rare in children (if present, investigate for cystic fibrosis)
  • Present in 20-50% of patients with asthma; 60-70% of patients with aspirin-exacerbated respiratory disease (AERD)

Aetiology

  • Chronic eosinophilic inflammation of the sinonasal mucosa
  • Associated conditions: chronic rhinosinusitis, asthma, allergic fungal rhinosinusitis, AERD (Samter's triad), cystic fibrosis, primary ciliary dyskinesia (Kartagener syndrome), Churg-Strauss syndrome (EGPA)
  • Type 2 inflammation: IL-4, IL-5, IL-13 driven eosinophilic infiltration
  • Not caused by allergy per se, but allergic rhinitis is a common comorbidity

Pathophysiology

  • Chronic inflammation leads to oedematous thickening of the sinus mucosa
  • Prolapse of oedematous mucosa through sinus ostia into the nasal cavity
  • Eosinophilic infiltration predominates; driven by type 2 cytokines (IL-5, IL-13)
  • Epithelial barrier dysfunction and Staphylococcus aureus superantigens contribute
  • Polyps cause mechanical obstruction, impaired mucociliary clearance, and olfactory dysfunction
  • Recurrence after surgical removal is common due to underlying mucosal disease

Clinical Presentation

Symptoms

  • Nasal obstruction (bilateral, progressive)
  • Anosmia/hyposmia (often the most troublesome symptom)
  • Nasal discharge (mucoid or mucopurulent)
  • Post-nasal drip
  • Facial pressure/fullness
  • Snoring
  • Headache (if sinus involvement)

Examination

  • Anterior rhinoscopy/nasal endoscopy: pale, grey, smooth, glistening, insensitive, pedunculated masses
  • Bilateral in most cases
  • Originate from middle meatus (ethmoid sinus mucosa)
  • Do NOT bleed on touch or cause pain (insensitive — distinguishes from turbinates)

Red Flags

  • Unilateral polyp in adult — biopsy to exclude inverted papilloma or malignancy
  • Nasal polyps in a child — investigate for cystic fibrosis (sweat test)
  • Bloodstained discharge or friable tissue (malignancy)
  • Facial deformity or proptosis (aggressive lesion)
  • Anosmia with polyps and asthma — consider AERD/Samter's triad

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Inferior turbinate hypertrophyRed, sensitive on palpation, responds to decongestantAnterior rhinoscopy
Inverted papillomaUnilateral, papillomatous surface, tends to recurCT, biopsy
Antrochoanal polypUnilateral, single large polyp from maxillary sinus, children/young adultsCT sinuses, nasal endoscopy
Sinonasal malignancyUnilateral, epistaxis, facial numbness, bony erosionCT/MRI, biopsy
Allergic fungal rhinosinusitisUnilateral, allergic mucin, eosinophilic, fungal hyphaeCT (hyperattenuating), biopsy
EncephalocoelePulsatile, blue mass, often at skull baseMRI (do NOT biopsy without imaging)

Diagnosis / Investigation

Bedside

  • Anterior rhinoscopy and nasal endoscopy
  • Assessment of nasal airflow
  • Smell testing

Bloods

  • Total IgE and specific IgE (allergic component)
  • Eosinophil count (type 2 inflammation marker)
  • Aspergillus-specific IgE (allergic fungal rhinosinusitis)
  • Sweat test: if polyps in a child (cystic fibrosis screening)
  • ANCA: if vasculitis suspected (EGPA)

Imaging

  • CT paranasal sinuses (non-contrast): gold standard
    • Mucosal thickening, opacification, polypoidal changes
    • Lund-Mackay score for severity grading
    • Pre-operative planning for FESS
  • MRI: if complications, malignancy, or skull base involvement suspected

Special Tests

  • Nasal peak inspiratory flow (NPIF): objective measure of nasal airflow
  • SNOT-22 questionnaire: validated quality of life measure for rhinosinusitis
  • Biopsy: for unilateral polyps (exclude malignancy/inverted papilloma)
  • Skin prick testing: for allergic rhinitis assessment

Management

Non-pharmacological

  • Saline nasal irrigation (daily, large-volume — NeilMed, sterile saline)
  • Allergen avoidance if allergic component identified
  • Smoking cessation

Pharmacological

  • First-line: intranasal corticosteroid drops or spray:
    • Mometasone 200mcg each nostril OD or fluticasone 200mcg each nostril OD
    • Betamethasone 0.1% drops (head-down position) — more effective for polyps than sprays
    • Long-term maintenance therapy
  • Short course oral prednisolone: 25-30mg OD for 5-10 days
    • For significant polyp load, acute exacerbation, or pre-operatively (to shrink polyps)
    • Limit to 2-3 courses per year (steroid side effects)
  • Biologics (for severe CRSwNP refractory to steroids and surgery):
    • Dupilumab (anti-IL4Rα): SC injection, NICE TA851 approved
    • Mepolizumab (anti-IL5): for severe eosinophilic CRSwNP
    • Omalizumab (anti-IgE): if concurrent allergic asthma
  • Antihistamines: if concurrent allergic rhinitis
  • Aspirin desensitisation: for AERD (specialist centre)

Surgical

  • FESS (functional endoscopic sinus surgery) with polypectomy:
    • Indicated when polyps refractory to maximal medical therapy (≥8 weeks of intranasal steroids + at least one course of oral steroids)
    • Removes polyps and opens sinus ostia to improve drainage and topical steroid access
    • Success rate for symptom improvement: 80-90%
  • Revision FESS: for recurrent polyps (recurrence rate 20-40% at 5 years)

Referral Criteria

  • ENT referral: nasal polyps visible on examination, chronic rhinosinusitis not responding to 3 months of medical therapy
  • Urgent/2-week wait: unilateral polyp (exclude malignancy), bloodstained discharge
  • Paediatric: nasal polyps in child (cystic fibrosis investigation)

Prognosis

  • Nasal polyps are a chronic condition with high recurrence after treatment
  • Intranasal steroids: reduce polyp size and improve symptoms in >60%
  • Oral steroids: rapid but temporary reduction in polyp size
  • Post-FESS: 80-90% symptom improvement; 20-40% polyp recurrence at 5 years
  • Biologics: significant improvement in polyp score, smell, and QoL in refractory patients
  • AERD/Samter's triad: more aggressive disease, higher recurrence rates
  • Anosmia: may not fully recover despite treatment
  • Long-term follow-up required with serial nasal endoscopy and SNOT-22 scoring

Other Relevant Information

Nasal Polyp Grading (Lildholdt Scale)

GradeDescription
0No polyps
1Small polyps not reaching below middle turbinate
2Polyps reaching below middle turbinate
3Polyps reaching lower border of inferior turbinate
4Polyps causing complete nasal obstruction

Samter's Triad (AERD)

ComponentPrevalence
Nasal polyps100% (by definition)
Asthma100% (often severe)
Aspirin/NSAID sensitivity100% (COX-1 inhibitor intolerance)
Eosinophilic inflammationPresent
TreatmentAspirin desensitisation, biologics, FESS

When to Investigate for Cystic Fibrosis

FindingAction
Nasal polyps in child <16 yearsSweat test
Bilateral polyps in young adultConsider CF testing
Polyps + recurrent chest infectionsSweat test, genetic testing