Enhanced Verifiable CPD from the
University of Birmingham

Aphthous Stomatitis
Exam Pass Notes

Key Takeaways

  • Very common oral mucosal condition characterised by recurrent aphthous ulcers
  • Exact cause unknown but involves immune system hyper-reactivity
  • Minor, major and herpetiform clinical types
  • Diagnose by clinical appearance, no testing needed usually
  • Treat with topical steroids, anaesthetics, antiseptics
  • May resolve spontaneously with age
  • Not infectious, not oral cancer

Introduction

  • Aphthous stomatitis is the most common disease of the oral mucosa, affecting about 20% of the population
  • It is characterised by recurrent formation of benign mouth ulcers (aphthae) in otherwise healthy people
  • Also called recurrent aphthous stomatitis (RAS) or canker sores
  • Onset often during childhood/adolescence, lasts for years before disappearing
  • No cure, treatment aims to manage pain and speed healing

Signs and Symptoms

  • Round or oval ulcer with yellow/grey fibrinous membrane, surrounded by red halo
  • Single or multiple ulcers, widely distributed in mouth
  • 3 types:
    1. Minor ulcers (<5mm), heal in 1-2 weeks (80-85% of cases)
    2. Major ulcers (>10mm), take weeks to heal, may scar (10% of cases)
    3. Herpetiform ulcers (multiple pinpoint ulcers, very painful, heal in <1 month)
  • Symptoms include burning/tingling before ulcer appears, pain worsened by acidic or abrasive foods

Causes

  • Exact cause unknown, likely multifactorial
  • Genetic predisposition in ~40%
  • Triggers: stress, trauma, nutritional deficiency, hormones, allergies, smoking, infections
  • Immune-mediated - T cells, cytokines like TNF-alpha involved
  • May be associated with autoimmune diseases

Immunology

  • Genetic types (HLA) linked but not definitive
  • Stress affects immune system
  • More common with immunodeficiency

Mucosal Barrier

  • More common on thinner non-keratinised mucosa
  • Atrophy of mucosa from nutritional deficiencies predisposes
  • Trauma decreases mucosal barrier
  • Hormones and contraceptives alter barrier
  • Smoking increases keratinisation, less common in smokers

Antigenic Sensitivity

  • Viruses like HSV, CMV detected but unclear role
  • Allergies to foods, toothpaste ingredients may trigger
  • Especially sodium lauryl sulphate (SLS) in toothpaste

Systemic Associations

  • Behçet's disease - severe oral/genital ulcers + uveitis
  • Blood deficiencies - B12, folate, iron
  • Coeliac disease - gluten sensitivity
  • Cyclic neutropenia - fluctuating neutrophils
  • Immunodeficiency e.g. HIV/AIDS

Diagnosis

  • Based on clinical appearance and history
  • Recurrent self-healing ulcers at regular intervals
  • Blood tests if severe/complex ulcers or systemic cause suspected
  • Patch testing for allergies
  • Biopsy not usually needed

Classification

  • Minor ulcers (<10mm), non-keratinised mucosa, heal in 1-2 weeks without scarring (80-85% of cases)
  • Major ulcers (>10mm), deeper, take 3-4 weeks to heal, may scar (10% of cases)
  • Herpetiform ulcers (<1mm), multiple, very painful, heal in <2 weeks without scarring

Treatment

  • Mainly topical agents - steroids, anaesthetics, antiseptics
  • Orabase, benzydamine, viscous lidocaine
  • Systemic meds like thalidomide for severe cases
  • Treat any nutritional deficiencies
  • Stress reduction, avoid trauma/allergens

Prognosis

  • Not serious, not oral cancer, not infectious
  • Symptoms range from minor nuisance to disabling
  • May resolve spontaneously in later life

Epidemiology

  • 20% lifetime prevalence
  • More common in developed nations, higher socioeconomic groups
  • Peak onset age 10-19 years
  • Lasts for years before disappearing
  • Equal in males/females
  • Possibly more common in individuals of Caucasian descent compared to those of African descent

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