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Evidence Levels: A Double-blind study B Clinical trial ≥ 20 subjects C Clinical trial < 20 subjects D Series ≥ 5 subjects E Anecdotal case reports
Primary burning mouth syndrome (BMS) is a rare, chronic, debilitating disease characterized by intraoral burning in the absence of systemic disease or identifiable abnormalities on physical examination and laboratory testing. Current evidence suggests that altered neurophysiology of the central or peripheral nervous system as well as immune-mediated, hormonal, and psychological factors may play an etiopathogenic role. The diagnosis of primary BMS is a clinical diagnosis of exclusion. Various medical conditions and medications can induce oral burning, a condition referred to as secondary BMS. Secondary BMS improves with treatment of the underlying condition(s).
A detailed history and physical examination should be completed to identify all alternative or correctable causes of oral burning. Correctable, associated factors may be local, systemic, or psychological.
Local factors include xerostomia (age, medication, radiotherapy); direct irritation (oral care products, tobacco); mechanical trauma (rough dental restorations, poorly fitting dental prostheses); parafunctional habits (bruxism, tongue thrusting); microbial infection or colonization (candidiasis, herpetic, fusospirochetal); geographic or fissured tongue; mucocutaneous diseases (lichen planus, pemphigus, pemphigoid); and allergic or irritant contact stomatitis (flavorings, food additives, dental materials, cosmetic products).
Systemic factors include nutritional deficiency states; autoimmune disease (Sjögren syndrome); gastrointestinal disease (gastroesophageal reflux); neurologic disease (trigeminal neuralgia, acoustic neuroma, Parkinson disease, glossopharyngeal neuralgia); medication(s); and endocrinopathies (hypothyroidism, diabetes).
Psychological factors include anxiety (including cancerophobia), depression, adjustment disorder, and psychosocial stressors.
Laboratory evaluation should be directed by the history and physical examination findings. If burning persists after eliminating or treating potential local, systemic, and psychological factors, a working diagnosis of primary BMS is adopted. Although consensus on treatment for primary BMS is lacking, many have found success with multimodal approaches resembling those used for the treatment of chronic, neuropathic pain.
Kohorst JJ, Bruce AJ, Torgerson RR, et al. Mayo Clin Proc 2014; 89(11): 1545–52.
Annual age- and sex-adjusted incidence of BMS of 11.4 per 100,000 person-years.
Jaaskelainen SK, Woda A. Cephalalgia 2017; 37: 627–47.
A review of BMS including evidence of neurophysiologic alterations in the peripheral or central nervous system.
Bogetto F, Maina G, Ferro G, et al. Psychosom Med 1998; 60: 378–85.
In a case-control study of 102 patients with BMS, 59.8% had concomitant psychiatric disorders.
Torgerson RR. Dermatol Ther 2010; 23: 291–8.
Multiple possible etiologies of BMS, including neuropathic, exocrine dysfunction, taste disturbance, mucosal atrophy, and psychological illness are reviewed ( Tables 33.1–33.3 ).
History | |
Oral symptoms | Timing, quality, duration, location, alleviating/exacerbating factors |
Medications | Causative: efavirenz, ACE inhibitors, ARBs, omeprazole, topiramate, TNF-α inhibitors |
Dental | Prostheses, recent procedures, dentifrices, topical medicaments, oral care products |
Parafunctional habits | Bruxism, tongue thrusting |
Review of symptoms | Weakness, headache, fatigue, concentration, sleep disturbance, arthralgia |
Physical examination | |
Oral | Complete oral examination, including head and neck (remove any dental prostheses) |
Nodal | Adenopathy |
Musculoskeletal | Temporomandibular joint |
Neurologic | Cranial nerve exam |
Hematologic | Complete blood count, ferritin, serum folate, cobalamin (+ methylmalonic acid, homocysteine) |
Metabolic | Serum thiamine, riboflavin, pyridoxine, zinc (+ alkaline phosphatase), magnesium |
Endocrinologic | Glycosylated hemoglobin, thyrotropin (+ free thyroxine) |
Immunologic | Antinuclear factor (+ Ro/SSA, La/SSB) |
Dermatologic | Biopsy (+ direct immunofluorescence) if visible abnormality on oral examination |
Microbiology testing | Herpes simplex (polymerase chain reaction [PCR]); varicella zoster (PCR); candidiasis (swab from site of pain for direct examination and culture); human immunodeficiency virus screening |
Otolaryngology | Nasopharyngoscopy |
Gastroenterology | Esophagogastroduodenoscopy |
Oral/maxillofacial | Periapical radiographs, magnetic resonance imaging |
Mental health | Psychiatry consultation |
Neurology | Neurologic examination, magnetic resonance imaging |
Hypersensitivity testing | Epicutaneous patch testing (preservatives, oral flavors, metals, adhesives, food-related allergens) |
Rabiei M, Leili EK, Alizadeh L. Contemp Clin Dent 2018; 9: S256–60.
Age and sex are significant risk factors for development of BMS. Menopause, candidiasis, psychological disorders, job status, dentures, and dry mouth were more common in patients with BMS.
Bender SD. Dent Clin North Am 2018; 62: 585–96.
BMS is a multifactorial condition, including interaction of psychological and neurophysiologic factors.
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Main DM, Basker RM. Br Dent J 1983; 154: 206–11.
A high rate of intraoral burning attributable to shortcomings in denture design.
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