Trigeminal Neuralgia

BASICS

BASICS

BASICS

DESCRIPTION

DESCRIPTION

DESCRIPTION

  • Trigeminal neuralgia (TN) is a painful disorder of the sensory nucleus of the 5th cranial (trigeminal) nerve that commonly produces episodic, paroxysmal, severe, lancinating facial pain lasting seconds to minutes
  • Often precipitated by stimulation of well-defined, ipsilateral trigger zones: usually perioral, perinasal, and occasionally intraoral (e.g., by talking, washing your face, shaving, or exposure to cold air)
  • Subtypes:
    • Classical: secondary to neurovascular compression, as evidenced by MRI
    • Idiopathic: when the criterion for TN is met, with evidence on MRI or electrophysiologic testing, suggestion no apparent or visible etiology
    • Secondary: diagnosed based on fulfillment of criteria for TN but attributed to a separate causative comorbid condition. The three subtypes of secondary TN are attributed to multiple sclerosis (MS), space-occupying lesions (such as cerebellopontine angle tumors, meningioma, etc.), or other causes (1)[A]
  • System(s) affected: nervous
  • Synonym(s): tic douloureux; Fothergill neuralgia; trifacial neuralgia; prosopalgia

EPIDEMIOLOGY

EPIDEMIOLOGY

EPIDEMIOLOGY

Incidence

Incidence

Incidence

  • 4 to 29/100,000 per year
  • Mean onset of 55 years

Prevalence

Prevalence

Prevalence

Pregnancy Considerations
Teratogenicity of medication therapy limits their use during 1st and 2nd trimesters

ETIOLOGY AND PATHOPHYSIOLOGY

ETIOLOGY AND PATHOPHYSIOLOGY

ETIOLOGY AND PATHOPHYSIOLOGY

  • Compression of the trigeminal nerve root by an anomalous artery, vein, or tumor such as meningioma or acoustic neuroma.
  • Demyelination from compression, or other cause such as MS, leads to an ectopic impulse generation with erratic responses such as hyperexcitability of damaged nerves and transmission of action potentials along adjacent, undamaged, and unstimulated sensory fibers.

Genetics

Genetics

Genetics

  • Prevalence of familial TN is about 1–2%.
  • Autosomal dominant inheritance pattern suggested
  • Other presentations may be attributed to gene mutations of calcium channels, sodium channels, MPZ gene, etc.

RISK FACTORS

RISK FACTORS

RISK FACTORS

MS associated with a 20-fold increased risk of developing TN

COMMONLY ASSOCIATED CONDITIONS

COMMONLY ASSOCIATED CONDITIONS

COMMONLY ASSOCIATED CONDITIONS

  • Sjögren syndrome; rheumatoid arthritis
  • Acute polyneuropathy
  • Charcot-Marie-Tooth neuropathy

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