Burning Mouth Syndrome

Nurdiana, drg., Sp.PM DEFINITION

“Burning Mouth Syndrome” (BMS)

oral burning  /other mucous membranes  no detectable cause, anatomic pathways, mucosal lesions, neurologic disorders & lab abnormalities Burn•ing syndrome

Scalded mouth Glossopyrosis syndrome BMS

Glossodynia Stomatodynia EPIDEMIOLOGY

>>> post Women 7 x : menopausal Men affected Prevalence men  >>> 3 – 12 women  at a later  0.7 - recent data years after mid – late age than 2.6%  male = 50s  10 - women female 15% ETIOLOGY

Unknown

Local Systemic Psychological

• Candida • Bacteria • Pre-Ca/Ca Local • Denture • Iritation/alergy • Pseudomembranous & erythematous candidiasis  BMS Candida No clinical signs of candidiasis  antifungal  86% improved & 13% Streptococci

Staphylococci Anaerobes

Bacteria Pre-Ca/Carcinoma

Leukoplakia/  burning/painful sensation Ca  itching/burning  premonitory symptom Denture

Main & Basker  ill-fitting  single greatest contributor

Faulty denture design  functional stress level to circum oral/lingual muscle 

Denture  fix  BMS persist Iritation/Alergy

Mechanical irritation  oral habit, denture design errors & sharp teeth

Chemical allergy  food, oral hygiene products or dental materials (methyl-methacrylate/mecury)

Contact allergy  inflammatory, lichenoid, or ulcerative lesions Xerostomia

Altered Glass : xerostomia sympa•thetic  local output  stress Xerostomia  BMS contributing factor, Salivary or alterations in incidence   no other authors : composition interactions clear association xerostomia  changes  BMS between cranial higher/lower  nerves & pain ??? sensation

• Menopause • Deficiency Systemic • DM • Nerve injury • Drugs

Hormonal changes  incidence BMS   hypoestrogenemia  Menopause mechanism unclear  usually not reversible with hormone replacement therapy Deficiency

BMS  symptoms of deficiency iron, Vitamin B & folic acid

Lamey et al  replacement vitamin B1, B2 & B6  effective in treating 88% BMS patients

Lab. abnormal  management & correction  BMS persist Xerostomia & candidiasis

Diabetes Mellitus After glucose control  BMS Diabetic persist, oters: diabetic neuropathy  treatment  BMS resolved  ??? head & neck region Characteristic post-traumatic nerve injury  alterations in Nerve Injury perception to touch, temperature, two-point discrimination & threshold pain  BMS infrequent Angiotensinconverting enzyme resolved after Drugs (ACE) inhibitors (, discontinuation of enalapril, & lisinopril) medication Psychological

Psychogenic problem  personality & mood changes  pain

Depression &  affect pain or secondary to chronic pain

Lamb et al: BMS  psychological factor & anxiety  most difficult to control

Psychological component  chronic low-grade trauma  parafunctional habits eg. rubbing tongue to the teeth or pressing tongue on  BMS

Symptom of cancer-phobia  reassuring  often helpful

More than one factor may be contributing BMS  one another, no specific etiology can be identified CLINICAL FEATURES

> 50%  onset spontaneous, no Most common sites : anterior identifiable precipitat•ing factor  ± 1/3 tongue, anterior hard palate, & onset with dental procedure, recent lower & often occurs in > one illness or medication course oral site

Burning  intermittent/constant Pain intensity & other symptoms   eating, drinking, or gradually  & persist for years candy/chewing gum  relieves symptoms. Local anesthetic elixir  burning  but  Moderate - severe intensity  gradually Mood changes  irritability & throughout the day  max intensity: late decreased desire to socialize  evening  difficulty falling asleep & related to altered sleep patterns experiencing interrupted sleep

Frequently accompanied by dry Additional complaints  facial mouth & thirst  no evidence of pain & pain at other sites decreased salivary flow PATHOGENESIS

• Completely unknown

Biochemical & pathophysiologic Injury/disease changes in nociceptive neurons in CNS Morphologic alterations in peripheral tissue BMS

Result of common systemic/local disorders nerve damage occurs to trigeminal nerve directly or other cranial nerves

inhibit oral nociceptive activity

Detailed history

Clinical examination DIAGNOSIS Lab

Exclusion of all other possible oral problems DIAGNOSIS

• Diagnosis : detailed history, clinical examination, lab studies & exclusion of all other possible oral problems • Key to diagnosis  history taking • Characteristics  sudden or intermittent onset of pain, bilateral, progressive during the day & remission with eating • Unilateral symptoms  thorough evaluation of trigeminal & other cranial nerves  eliminate neurologic source of pain • Complain  xerostomia + burning  evaluation of salivary gland disorder  mucosa dry & difficulty swallowing dry foods • Ruled out potential causes even typical features of BMS present • Burning persists after management sys•temic or local oral conditions  diagnosis of BMS can be considered

Making clinical diagnosis  not difficult, determining etiology  difficult LABORATORY STUDIES

C. albicans culture Biopsy  not indicated  no Sjogren's syndrome clinical lesion is antibodies serum tests Individual associated consideration  complete blood count depend on history & clinical suspicion serum iron, total iron- binding capacity

serum B12 & folic acid levels MANAGEMENT

• First  exclude other disease • Sources of pain must be eliminate  not too much expectation

True BMS • Education : – Reassured  benign nature of condition & frightening possibilities (cancer)  can be excluded – If suggests psychogenic factors  explain that & other emotional disturbances can cause physical diseases • Instruction : – Counseling & reassurance  adequate for mild BMS  more severe symptoms  drug therapy – Parafunctional oral habits  eliminate  splint covering teeth and/or palate • Therapy : – Low doses tricyclic (TCA) : amitriptyline, desipramine, nortriptyline, imipramine, clomipramine, or doxepin – Should be stressed  drugs not to manage psychiatric illness  analgesic effect – Benzodiazepines : clonazepam (benzodia-zepine derivative) & GABA (gamma-aminobutyric acid) receptor agonist  effective for various disorder – Grushka et al  clonazepam effective in relieving taste dysgeusia & oral dryness along with BMS – Topical capsaicin  monoamine oxidase inhibitor tranylcypromine sulphate in combination with diazepam  neuropathic pain conditions PROGNOSIS

• Partial remissions  occur in approximately 2/3 patients  in 6 – 7 years after onset • No studies investigated whether earlier intervention or earlier & better pain control  lead to earlier disease remission