facial pain

Facial pain

Introduction Head, neck, and orofacial pain classifications Intracranial disorders 1- Neurovascular headache disorders 2- Neuropathic pain disorders Extracranial pain disorders 1- Intraoral pain disorders 2- Musculoskeletal cervical and temporomandibular disorders 3- Cervical spine disorders 4- Temporomandibular disorders 5- Muscular disorders Local myalgia Myofascial pain Centrally mediated myalgia Myospasm Myositis and tendonitis Muscle contracture Muscle neoplasia


Intracranial and vascular pain disorders - Neurovascular headache disorders: Primary headache Secondary headache - Neuropathic pain disorders: Proxysmal pain disorders Continuous pain disorders - Headache attributed to associated extracranial pain disorders: Eye, ear, nose, sinuses, and throat disorders - Extracranial intraoral pain disorders Teeth and periodontal disorders Mucogingival, tongue, salivary gland disorders - Musculoskeletal pain disorders - Cervical disorders - Temporomandibular disorders: Articular disorders Muscular disorders


Investigations clinical signs and symptoms clinical examinations Radiographic exam, CT or/and MRI

Trigeminal neuralgia

Definition Disorder of the fifth cranial nerve leading to intense paroxysmal pain within one or more divisions of its sensory supply. Epidemiology 3-6/100.000, more common in female. Incidence of severity increase with age. Usual age of onset 50-70 years

Trigeminal neuralgia

Cause: compression of trigeminal nerve root by artery in middle cranial fossa nerve demyelination Clinical: Paroxysmal pain within one of the three divisions of trigeminal n, usually maxillary and mandibular divisions. intense, lancinating, burning pain, ‘’ like an electric shock)Pain last seconds to minutes onlyFrequency varies, may be multiple times/hourAlmost always unilateral Many patients have a trigger point for their pain, which may be stimulated by everyday tasks, such as eating, talking and washing Patients have periods of remission and relapse, but symptoms tend to worsen over time. Neurological examination shows no clinical abnormality

Trigeminal neuralgia

Investigation Full neurological examination MRI brain if: Atypical features Possible underlying demyelinating disease or intracranial lesion Microvascular decompression Treatment: Medical management (first line) Anticonvulsant, such as carbamazepine, phenytoin or gabapentin, or a combination. Carbamazepine started as 100 mg twice daily, up to 1600mg/day monitor WBC and liver function require close follow-up and trial reductions of therapy once symptom free


Trigeminal neuralgia
Surgical Management Peripheral procedures eg. cryotherapy/ chemical destruction with alcohol/ phenol. Radiofrequency ablation to affected branch under LA / GA central neurosurgical procedures. Artery causing nerve compression is separated from nerve using Teflon sheet Gamma knife (radiosurgey) All the above carry risks of permanent paraesthesia, anaesthesia dolorosa (sever continous pain within the distribution of the nerve), and risks associated with the surgical procedure itself. Therefore the surgical approach applied when medical management side effect are intolerable

Migraine

Definition primary recurrent headache disorder, more common in females. Termed hemicrania as it effects half of the head. Cause possibly related to abnormal 5-hydroxytryptamine (5-HT) receptors activity leading initially to vasoconsitrction of portions of cerebral arteries followed by compensatory vasodilation with cerebral oedema and pain. Precipitants include: Hormonal factors Dietary, e.g chocolate, bananas stress sleep deprivation Bright or flashing lights

Migraine

Clinical signs and symptoms May have preceding aura: visual hallucination, including flashing coloured lights, loss colour perception or other visual disturbances motor- temporary muscle palsies speech disorders including aphasia Sever unilateral headache : Initially poorly localised Becomes localised to temporal, frontal or orbital region. Photophobia Nausea Vomiting Treatment Acute attack: analgesics, sumatriptan (5-HT antagonist), ergot derivatives. Prophylaxis: options include pizotifen (antihistamine), propanolol calcium channel blockers.

Cluster Headaches

DefinitionRecurrent headaches typically around the eye.also known as migrainous neuralgia and Horton’s syndrome. Occur in intermittent bouts with interspersed periods of remission. Often positive family history. 80% patients smoke. Presents in third or fourth decade.EpidemiologyLess common than migraine. male: female = 6:1CauseUnknown. Possible allergic basis with mast cell release of histamine and vasodilatation, Associated with: sleep apnoea and decrease oxygen saturations. AlcoholCocaine

Cluster Headaches

Clinical sign and symptom:Severe, unilateral episodes of burning or lancinating pain, in and around the orbit, frontal and temporal region.Sudden onset, lasts for 15min – 3 hours, often awakens the patient at night.Begin at same time every day (Alarm clock headache)May have multiple episodes each dayOccur for 2- 3 months, then have periods of remission that can last for years.May be associated with autonomic problems:Conjunctival vessel congestion Eye watering and swelling around the eyeNasal congestionFacial flushing

Cluster Headaches

Investigation Diagnosis is clinical. However similar symptoms may be secondary to intracranial pathology, so consider MRI of the brain. Treatment Acute attack: 1- Oxygen may abort an attack and its effectiveness is diagnostic 2- Subcutaneous or intranasal Sumitriptan Prophylaxis: Nifedipine Ergotamine


Temporal (giant cell) arteritis

Temporal (giant cell) arteritis

Atypical facial pain

Atypical facial pain

Investigation All imaging (including intracranial MRI), bloods, and biopsies are normal Treatment Often unrewarding with limited response Tricyclic antidepressants have some effect in some patients About 30% will respond to gabapentin The involvement of a pain team with access to psychological therapy may help patients to manage their pain

Burning mouth syndrome

Burning mouth syndrome