14.4 Trigeminal Neuralgia, Bell's Palsy and Giant Cell Arteritis
Key Takeaways
- Trigeminal neuralgia causes paroxysmal electric-shock pain lasting seconds to two minutes and is treated first line with carbamazepine.
- Bell's palsy is treated with oral prednisolone 50 to 60 mg daily for 10 days started within 72 hours, together with eye protection.
- Bell's palsy is a lower motor neuron lesion affecting the forehead, which distinguishes it from a stroke.
- Jaw claudication with scalp tenderness in an older patient suggests giant cell arteritis, which requires same-day high-dose corticosteroid to prevent irreversible blindness.
- Long-term phenytoin therapy causes gingival enlargement that begins at the interdental papillae.
3. Neurological Conditions: Epilepsy, Stroke, and Cranial Neuropathies
Cranial Neuropathies: Trigeminal Neuralgia, Bell's Palsy, and Giant Cell Arteritis
Cranial Neuropathies
│
┌─────────────────────────────────┼─────────────────────────────────┐
▼ ▼ ▼
Trigeminal Neuralgia (CN V) Bell's Palsy (CN VII) Giant Cell Arteritis (GCA)
• Unilateral, lancinating • Acute idiopathic LMN • Systemic vasculitis (>50 yrs)
paroxysms (V2 / V3) paralysis of whole face • Temporal headache, scalp
• Triggered by light touch • Forehead paralysed tenderness
• Normal neuro exam • Bell's phenomenon • Pathognomonic Jaw Claudication
• Rx: Carbamazepine / MVD • Rx: Prednisolone (72 hrs) • Visual loss emergency (AION)
• Corneal eye protection • Rx: High-dose Prednisolone
| Feature | Trigeminal Neuralgia (Tic Douloureux) | Bell's Palsy (Idiopathic CN VII Palsy) | Giant Cell Arteritis (Temporal Arteritis) |
|---|---|---|---|
| Anatomical Target | Trigeminal Nerve (predominantly V2 & V3) | Facial Nerve (CN VII motor trunk) | Medium/large cranial arteries (extracranial branches of ECA) |
| Patient Demographics | Adults $> 50\text{ years}$; females > males | Any age (peak 20–40 years); equal sex | Exclusively adults $> 50\text{ years}$ (peak 70–80 years); females 3:1 |
| Clinical Hallmarks | Unilateral, excruciating, paroxysmal, electric-shock pain lasting seconds to 2 minutes | Acute, unilateral, complete flaccid paralysis of all facial expression muscles, including forehead | Severe temporal headache, scalp tenderness, jaw claudication during chewing |
| Provoking Factors | Non-painful tactile stimuli to trigger zones (shaving, washing face, brushing teeth, light breeze) | Acute idiopathic (often post-viral reactivation within fallopian canal) | Provoked by continuous mastication (ischaemia of masseter/temporalis) |
| Neurological Exam | Normal sensory and motor exam (no sensory deficit) | Lower Motor Neurone (LMN) facial palsy; loss of forehead wrinkling; eye closure failure | Tender, swollen, nodular, pulseless superficial temporal artery |
| Medical Management | Carbamazepine (100–1200 mg/day); oxcarbazepine; Microvascular Decompression | Oral Prednisolone (50–60 mg/day for 10 days) within 72 hours; Eye protection | IMMEDIATE Emergency high-dose Prednisolone (60 mg/day) to prevent permanent blindness |
Trigeminal Neuralgia (Tic Douloureux)
- Clinical Presentation: Paroxysms of sudden, unilateral, lancinating, electric-shock-like, stabbing pain strictly localized along the anatomical distribution of one or more divisions of the trigeminal nerve. The maxillary (V2) and mandibular (V3) divisions are involved in $>95%$ of cases; the ophthalmic (V1) division is affected in $<5%$. Paroxysms last from a few seconds up to 2 minutes, followed by a refractory period during which further pain cannot be triggered.
- Trigger Zones: Pain is provoked by trivial non-noxious tactile stimuli applied to cutaneous or mucosal trigger zones: washing the face, shaving, tooth brushing, eating, talking, or a cold breeze.
- Diagnostic Distinction: In classical trigeminal neuralgia, the neurological sensory examination is completely normal. The presence of sensory loss (numbness, hypoaesthesia) indicates secondary trigeminal neuralgia (e.g., multiple sclerosis plaque or acoustic neuroma compressing the nerve root), requiring urgent brain MRI.
- Differentiation from Odontogenic Pain: Unlike acute pulpitis, trigeminal neuralgia pain is non-continuous, is not provoked by thermal liquids, lacks periapical radiographic pathology, and follows discrete refractory cycles.
- Management: Medical first-line therapy is Carbamazepine (100 mg twice daily, titrated up to 800–1200 mg daily; monitor full blood count for agranulocytosis and liver function). Surgical treatment: Microvascular Decompression (Jannetta procedure) via posterior fossa craniotomy to lift an aberrant arterial loop (most commonly the superior cerebellar artery) compressing the trigeminal root entry zone at the pons.
Bell's Palsy
Bell's palsy is an acute, isolated, idiopathic Lower Motor Neurone (LMN) paralysis of the facial nerve (CN VII):
- Clinical Signs: Rapid onset (peaks within 48 hours) of complete unilateral facial weakness:
- Inability to raise the eyebrow or wrinkle the ipsilateral forehead (frontalis paralysis).
- Inability to close the eye (orbicularis oculi paralysis); on attempted closure, the eyeball rolls upward and outward (Bell's phenomenon).
- Drooping of the corner of the mouth, loss of the nasolabial fold, drooling of saliva, and flattening of the cheek (buccinator/orbicularis oris paralysis).
- Hyperacusis (loss of stapedius muscle dampening) and loss of taste on the anterior two-thirds of the tongue (chorda tympani involvement).
- UMN vs LMN Facial Nerve Palsy: In an Upper Motor Neurone lesion (e.g., Stroke), the muscles of the upper face (forehead and eye closure) are spared because the dorsal portion of the facial motor nucleus in the pons receives bilateral corticonuclear innervation from both cerebral hemispheres. In an LMN lesion (Bell's palsy), the final common motor pathway is severed, causing complete paralysis of the entire ipsilateral face, including the forehead.
- UK Treatment Guidelines (NICE): Prescribe early high-dose oral corticosteroids: Prednisolone 50 to 60 mg daily for 10 days, initiated within 72 hours of symptom onset to reduce perineural oedema within the narrow osseous facial canal.
- Corneal Protection: The primary complication is exposure keratitis, corneal ulceration, and permanent blindness due to the inability to blink or close the eye. The dentist/doctor must prescribe lubricating eye drops (artificial tears) by day, ophthalmic lubricating ointment at night, and instruct the patient to tape the eyelid closed or wear an eye patch while sleeping.
Giant Cell Arteritis (Temporal Arteritis)
Giant cell arteritis (GCA) is a systemic granulomatous panarteritis of medium- and large-sized arteries, preferentially targeting extracranial branches of the carotid arteries (superficial temporal, ophthalmic, and facial arteries):
- Demographics: Occurs exclusively in patients over 50 years of age (median age 75); strong association with polymyalgia rheumatica (stiffness in shoulder and pelvic girdles).
- Pathognomonic Triad:
- Severe, new-onset unilateral temporal or occipital headache.
- Scalp tenderness: Severe pain elicited by simple tactile contact, such as combing hair or resting the head on a pillow.
- Jaw Claudication: Occurs in ~50% of patients. Severe fatigue, aching, or cramping pain in the masseter and temporalis muscles provoked specifically by mastication or continuous talking, which rapidly resolves upon resting the jaw. It is caused by reversible ischaemia in the branches of the maxillary artery supplying the masticatory apparatus.
- The Catastrophic Hazard — Irreversible Blindness: Occlusion of the posterior ciliary arteries (branches of the ophthalmic artery) produces Anterior Ischaemic Optic Neuropathy (AION), resulting in sudden, painless, permanent, irreversible blindness in the affected eye, which can spread to the contralateral eye within hours to days.
- Investigations: Profoundly elevated inflammatory markers: Erythrocyte Sedimentation Rate (ESR) typically $> 50-100\text{ mm/hr}$ and elevated C-Reactive Protein (CRP). Definitive diagnosis: Temporal Artery Biopsy (TAB) demonstrating transmural granulomatous infiltrate with multinucleated giant cells and fragmentation of the internal elastic lamina.
- Emergency Dental Action: Giant cell arteritis is a medical ophthalmic emergency. If a dental patient presents with new temporal headache and jaw claudication, the dentist must immediately refer the patient to the emergency eye hospital or acute rheumatology service on the same day. High-dose systemic corticosteroids (oral Prednisolone 60 mg daily, or IV methylprednisolone) MUST be commenced immediately without waiting for biopsy results to preserve vision.
4. Clinical Traps, Diagnostic Pitfalls, and Worked Scenarios
[!CAUTION] Clinical Trap: Misdiagnosing Jaw Claudication as Temporomandibular Disorder (TMD): A 74-year-old female presents with bilateral pain in her masticatory muscles when chewing hard foods. The practitioner palpates tender masseter muscles and diagnoses myofascial pain dysfunction syndrome (TMD), fitting an acrylic occlusal splint. Two weeks later, the patient wakes up completely blind in her right eye. A detailed history would have revealed severe scalp tenderness when brushing her hair and a continuous right temporal headache. In any patient over 50 presenting with "jaw pain when chewing", giant cell arteritis must be actively excluded before diagnosing TMD.
[!WARNING] Clinical Trap: Dental Extractions in Undetected Severe Liver Cirrhosis: Performing routine dental extractions on a patient with chronic alcoholic cirrhosis without a recent clotting screen and full blood count is hazardous. Severe deficiency of hepatic clotting factors (II, VII, IX, X) combined with hypersplenism-induced thrombocytopenia and impaired fibrinogen synthesis can result in intractable, life-threatening post-extraction haemorrhage. In suspected liver impairment, always obtain a current INR, APTT, and platelet count, and have local haemostatic agents readily available.
Worked Clinical SBA Scenario
Scenario: A 76-year-old female presents to your dental surgery complaining of severe, cramp-like pain in both cheeks and temples that develops after approximately two minutes of chewing solid food, forcing her to pause eating until the discomfort subsides. She also notes a persistent right-sided throbbing headache over the past three weeks and states that brushing her hair has become intensely painful. Palpation reveals a prominent, tender, non-pulsatile cord-like swelling over the right superficial temporal artery. There is no joint clicking or TMJ tenderness.
Question: What is the most likely diagnosis, what catastrophic complication is imminent, and what is the immediate management required of the dental practitioner?
Analysis and Clinical Governance: The clinical presentation of jaw claudication provoked by chewing solid food, combined with severe scalp tenderness when brushing hair and a unilateral temporal headache in a patient over 50 years of age, is classic for Giant Cell Arteritis (Temporal Arteritis). The non-pulsatile, tender temporal artery reflects transmural granulomatous panarteritis. The most catastrophic risk is irreversible, permanent visual loss due to ischaemic optic neuropathy from posterior ciliary arterial occlusion. The dentist must recognize this as an acute medical emergency and arrange immediate same-day referral to an emergency ophthalmology department or acute medical team, ensuring high-dose oral corticosteroid therapy (Prednisolone 60 mg daily) is initiated immediately to safeguard the patient's vision.
A 73-year-old female presents to the dental clinic with severe bilateral aching pain in her masseter and temporalis muscles provoked specifically by chewing solid food, which resolves completely within minutes of resting her jaw. She also reports a new-onset right-sided headache and painful sensitivity when brushing her hair. Palpation of the right superficial temporal artery reveals a tender, swollen, pulseless cord. What is the immediate clinical obligation of the dentist?
A 28-year-old male with long-standing epilepsy managed with phenytoin attends for a dental extraction. During the procedure, the patient suddenly loses consciousness and develops generalized tonic-clonic convulsions. The seizure continues unremittingly for 6 minutes. What is the diagnosis, and what is the mandatory immediate medical intervention?