Upload
cocomathew
View
16
Download
0
Embed Size (px)
DESCRIPTION
latest notes on BMS etio patho and management
Citation preview
Burning mouth syndrome
Lisa A. Drage, MD*, Roy S. Rogers III, MD
Department of Dermatology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA
The burning mouth syndrome (BMS) is defined as
a symptom complex of those patients with mouth
pain who have a clinically normal oral mucosal
examination. BMS is a diagnosis of exclusion. Many
oral mucosal diseases present with mouth pain; a few
examples include lichen planus, recurrent herpes
simplex virus infections, and recurrent aphthous
stomatitis. A thorough oral examination must be
completed to exclude these and other oral diseases
before diagnosing BMS. Synonyms for BMS have
included glossodynia, glossopyrosis, glossalgia, sto-
matodynia, stomatopyrosis, sore tongue and mouth,
burning tongue, oral or lingual paresthesia, and
oral dysesthesia.
Burning mouth syndrome is often stereotyped as a
purely psychosomatic disorder occurring in postmen-
opausal women, which is resistant to therapy.
Although BMS can be a diagnostic and therapeutic
challenge, multiple studies have linked BMS to real
organic and psychiatric disease and show an improve-
ment in symptoms in about 70% of patients with
directed therapy [16]. Faced with a patient who has
BMS, dermatologists and other clinicians need to be
familiar with its associations and management, and
optimistic about potential outcome.
The patient variably describes a burning, tingling,
painful, hot, scalded, or numb sensation in the oral
cavity. The magnitude of BMS pain is quantitatively
similar to a toothache [7]. This sensation occurs most
commonly on the anterior two thirds and tip of the
tongue. Multiple oral sites may be involved. These
may include the upper alveolar region, palate, lips,
and lower alveolar region [1,2,5,6,8]. Less commonly
affected are the buccal mucosa, floor of the mouth,
and the throat [4]. With prevalence in the general
population of 3.7% [9], BMS affects women seven
times more frequently than men [5]. It particularly
affects the middle-aged and elderly population (mean
age 60) [2,6,10] and has not been reported in children.
The average duration of BMS is 2 to 3 years [2,11],
with rare patients suffering for decades. Most BMS
patients have consulted multiple dentists, physicians,
and other health care providers for their complaint and
may have tried a host of over-the-counter and pre-
scription medications before their presentation [2,4].
Over half state they received insufficient information
about BMS from their health care provider [12].
Burning mouth syndrome has been divided into
three subtypes based on the daily variation of the
symptoms (Table 1) [13]. Type 1 BMS (35%) is
characterized by daily pain that is not present on
awakening but progresses throughout the day with
the greatest problems occurring in the evening hours.
Type 2 BMS (55%) patients awake with a constant
daily pain, whereas Type 3 BMS (10%) patients have
intermittent pain with symptom-free intervals and the
pain occurs in unusual sites, such as the buccal
mucosa, floor of mouth, and throat. Nonpsychiatric
factors have been linked with Type 1 BMS, chronic
anxiety with Type 2, and food additives or flavoring
allergies with Type 3 BMS. The patients with Type 2
BMS tend to be most resistant to therapy [13,14].
Associated factors
Many conditions have been associated with BMS
(Table 2) [2]. It should not be surprising that oral pain
like any type of pain can have more than one cause.
The four main categories are (1) systemic, (2) local,
0733-8635/03/$ see front matter D 2003, Elsevier Science (USA). All rights reserved.
PII: S0733 -8635 (02 )00063 -3
* Corresponding author.
E-mail address: [email protected] (L.A. Drage).
Dermatol Clin 21 (2003) 135145
(3) psychiatric or psychologic, and (4) idiopathic
factors. The most common associations include psy-
chiatric or psychologic disorders, xerostomia, nu-
tritional deficiencies, allergic contact stomatitis,
denture-related factors, parafunctional behavior, can-
didiasis, diabetes mellitus, and menopause or hor-
monal alterations [2].
Multifactorial
In more than a third of patients, multiple, concur-
rent causes of BMS may be identified and need to be
addressed simultaneously to achieve the best outcome
possible [15,12,15].
Psychiatric or psychologic disorders
Psychiatric disease is a common underlying factor
in patients with BMS. A psychiatric disease asso-
ciation has been reported in many series ranging from
19% to 85% [35,9,11,1325]. At least one third of
patients may have an underlying psychiatric diag-
nosis, most commonly depression or anxiety disor-
ders [2]. A phobic concern regarding cancer is also
Table 1
Lamey classification of subtypes of BMS [13]
Clinical course Association
Type 1 Daily pain, not present on awakening, increases throughout day Nonpsychiatric
Type 2 Daily pain, constant Psychiatric, especially chronic anxiety
Type 3 Intermittent pain, unusual sites (buccal mucosa, floor of mouth) Allergic contact stomatitis to flavorings, additives
From Lamey PJ, Lamb AB, Hughes A, et al. Type 3 burning mouth syndrome: psychological and allergic aspects. J Oral Pathol
Med 1994;23:2169; with permission.
Table 2
Reported etiologic agents of BMS [2]
Systemic Local Psychogenic and psychiatric Idiopathic
Deficiencies Denture factors Psychiatric
Iron Dental work Depression
Vitamin B12 Mechanical Anxiety
Folate Oral habit or parafunctional behavior Obsessive compulsive disorder
Zinc Clenching Somatoform disorder
B complex vitamins Bruxism Cancerphobia
Endocrine Tongue thrusting Psychosocial stressors
Diabetes mellitus Myofascial pain
Hypothyroidism Allergic contact stomatitis
Menopause or hormonal Dental restoration or denture materials
Foods
Xerostomia Preservative, additives, flavorings
Connective tissue disease Neurologic
Sjogrens syndrome Referred from tonsils or teeth
Sicca syndrome Lingual nerve neuropathy
Drug-related Glossopharyngeal neuropathy
Anxiety or stress Acoustic neuroma
Medication Infection
ACE inhibitor Candidiasis
Esophageal reflux Antibiotic related
Anemia Denture related
Local trauma
Corticosteroid
Diabetes mellitus
Fusospirochetal
Xerostomia
Irradiation
Local disease
From Drage LA, Rogers RS III. Clinical assessment and outcome in 70 patients with complaints of burning or sore mouth
symptoms. Mayo Clin Proc 1999;74:2238; with permission.
L.A. Drage, R.S. Rogers III / Dermatol Clin 21 (2003) 135145136
prominent in 20% of patients [5]. The BMS patient
may be concerned that the symptoms are caused by
oral or systemic cancer, although the patient rarely
shares this concern spontaneously with the physician.
Repeated self-examination may be a marker for
cancerphobia [4].
Although BMS may be a somatic symptom of
depression in some cases, the association does not
always equate to a causal relationship. Depression and
psychologic disturbance are common in chronic pain
populations and may be secondary to chronic pain
rather than the cause of BMS. Studies have reported
similarities between the personality characteristics of
chronic oral pain patients and other chronic pain
populations [7]. Similar sleep disturbances have also
been documented in these populations [8]. In addition,
many of the medications used to treat psychiatric
disease can cause xerostomia and exacerbate BMS.
Although psychiatric disorders are clearly sig-
nificant for some patients with BMS, it is important
not to leap to the conclusion that all BMS is caused
by psychiatric problems. Unfortunately, psychiatric
causes are frequently postulated when no easy
answer is apparent. Each patient with BMS should
receive a careful evaluation for both psychiatric and
organic causes of pain. This thorough examination
may unveil a local or systemic cause for their
symptomatology and is often therapeutic, reassuring
the patient about concerns regarding oral cancer.
During the evaluation, direct questions about depres-
sion, anxiety, and fear of cancer and a family history
of psychiatric disorders or oral cancer should be
posed. When warranted, further evaluation and docu-
mentation of psychiatric disease by psychiatric con-
sultation should be sought. A team approach is
important; psychiatric staff may not feel as comfort-
able confirming the diagnosis of BMS because they
are less familiar with oral disease.
Xerostomia
A dry mouth is a frequent complaint among BMS
patients and can be found in up to 25% [2,5,6] of
patients with these complaints. Decreased oral lu-
brication may result in increased friction and discom-
fort leading to BMS (Fig. 1). Xerostomia itself can be
multifactorial. Drug-related xerostomia is common
[2,22] and can occur with many medications includ-
ing tricyclic antidepressants, benzodiazepines, mon-
amine oxidase inhibitors, antihypertensives, and
antihistamines. Connective tissue diseases, such as
Sjogrens syndrome or sicca syndrome, can cause
xerostomia [2,8], as can a history of local irradiation
or diabetes mellitus. Even stress and anxiety can lead
to a dry mouth. Although hypothesized, age-related
or menopausal xerostomia has not been conclusively
documented [26].
Nutritional deficiencies
Because of rapid cell turnover and trauma, the oral
cavity is especially sensitive to nutritional deficien-
cies and may be the first indicator of such a problem.
Iron deficiency anemia, pernicious anemia (an auto-
immune B12 deficiency), zinc deficiency, and B
complex vitamin deficiency [20] have all been
reported to cause BMS. Nutritional deficiencies have
been claimed to cause BMS in as few as 2% [15] and
as many as 33% [1] of patients. The mucosal alter-
ations associated with these deficiency states, such as
erythema, glossitis, loss of papillae, or atrophy, may
be absent in BMS patients (Fig. 2). Replacement
therapy may be helpful in BMS patients with docu-
mented deficiencies [2,5,6,20,27].
Allergic contact stomatitis
The role of allergens in BMS is somewhat con-
troversial. Although some studies claim a high prev-
alence of allergy to dentures and dental materials,
such as acrylates, nickel, mercury, gold, and cobalt
[2830], more recent studies [2,31] were unable to
implicate denture or denture materials as a frequent
cause of BMS. Because true allergies to denture
materials are rare, patients should not be considered
allergic to denture or dental material until controlled
patch testing has been correlated with clinical symp-
Fig. 1. Xerostomia. A dry mouth is a common complaint of
patients with burning mouth syndrome (BMS). Note the dry,
erythematous, fissured tongue plus angular cheilitis.
L.A. Drage, R.S. Rogers III / Dermatol Clin 21 (2003) 135145 137
toms. Patients with Type 3 BMS (intermittent pain)
are more likely to have positive patch tests [13].
Flavoring or food additives have been implicated.
This subtype clearly merits patch testing. Lamey et al
[13] noted 65% of Type 3 BMS cohort had positive
patch tests and 80% of this group improved with
avoidance of the implicated allergen. Cinnamon alde-
hyde (cinnamon), sorbic acid, tartrazine, benzoic
acid, propylene glycol, menthol, and peppermint have
all been identified as potential causes of mouth pain
[2,13,31]. Note the contribution of LeSueur and
Yiannis on contact stomatitis elsewhere in this issue.
Denture-related problems
Pain affecting only denture-bearing tissue, a tem-
poral association with denture use, or improvement
with discontinuation of dentures is a clue to denture-
related BMS. Rather than an allergic response to
denture material, denture-related pain is usually
caused by faulty design, irritation, or parafunctional
behavior. Candidiasis can also contribute to denture-
related pain. Main and Basker [6] attributed BMS to
denture design faults in 50% of patients; with replace-
ment of dentures the patients improved. Lamey and
Lamb [5] noted 60% of BMS patients had denture
design faults, but only half of these patients improved
after denture replacement. The main denture design
faults of concern are (1) restricted tongue space, (2)
lack of freeway space, and (3) underextended denture
bases [4]. These denture design faults can increase the
stress on surrounding tissues or change the normal
function of the tongue. Most BMS patients with
dentures or significant dental work benefit from
referral for a formal dental consultation to assess
dental work, dentures, occlusion, and the need for
modification or replacement. This topic is addressed
by Kupp and Sheridan elsewhere in this issue.
Parafunctional behavior
Burning mouth syndrome associated with para-
functional behavior is probably more common than is
realized and is often under appreciated by physicians.
Lamey and Lamb [5] found parafunctional activity a
concern in 13% of a group of patients with BMS.
Patients who clench or grind their teeth, thrust their
tongue repetitively (Fig. 3), run their tongue against
Fig. 2. Smooth tongue. A smooth tongue is atrophic with
loss of filiform papillae. This permits an increased sen-
sitivity to irritants causing BMS. A smooth tongue may
indicate a systemic condition, such as pernicious anemia,
iron deficiency anemia, or gluten-sensitive enteropathy.
Fig. 3. Tongue thrusting. Parafunctional habits, such as
tongue thrusting, may cause, or occur secondary to, the
symptoms of BMS. Note the crenulated or scalloped borders
to the tongue. Similar findings are seen with macroglossia.
L.A. Drage, R.S. Rogers III / Dermatol Clin 21 (2003) 135145138
their teeth, or try to reseat an ill-fitting denture with
their tongue may develop oral pain. These behaviors
may be unconscious or may only occur at times of
stress. Examination of the tooth surface and dentures
can sometime give clues to parafunctional behavior.
Dental consultation may be helpful in identifying and
managing these behaviors.
Candidiasis
Reported as a causative factor in 6% [5] to 30%
[15] of patients with BMS, the mucosal alterations
typically associated with candidiasis may be minimal
or absent in BMS patients. Osaki et al [32] reported
subclinical candidiasis as a cause of BMS in 25% of a
patient cohort. Glossal pain subsided with treatment
with 3% amphotericin mouthwash solution. Oral
candidiasis is an opportunistic infection. A normal
constituent of the mouth in 40% of patients, candidal
overgrowth occurs with xerostomia, corticosteroid
treatment, antibiotic treatment, denture use, and dia-
betes mellitus. Empiric treatment for oral candidiasis
is often prescribed to patients with BMS.
Diabetes mellitus
Metabolic alterations in the oral mucosae, diabetic
neuropathy, and angiopathy are all proposed mecha-
nisms behind BMS in patients with diabetes mellitus.
Xerostomia and oral candidiasis may also contribute
to the problem. About 5% of BMS patients have
diabetes mellitus [4]. BMS is the second most com-
mon oral complaint after xerostomia in a study of
diabetic patients [1]. Control of diabetes mellitus may
lead to improvement or cure of BMS.
Menopause or hormonal alterations
Most patients seen by physicians for BMS are
women. All the literature on BMS finds that this
condition is more common in women than men with a
ratio of 7 to 1 [4]. Other oral pain syndromes are also
seen more commonly in women [33]. In light of the
prevalence of BMS in postmenopausal women, a role
for a hormonal impact on BMS has long been
suspected [1,34]. In controlled clinical trials with
systemic or local estrogen treatment, however, neither
was more effective than placebo in the treatment of
BMS [10,35]. No significant differences are found
between women with mouth pain and a control group
in number of years since menopause, use of estrogen
replacement therapy, or number of years of use of
estrogen replacement therapy [8,33]. Although
clearly a significant link between BMS and this age
group of women exists and may be tied with meno-
pause, there is currently no proven benefit of hor-
mone replacement therapy in BMS.
Drug-related BMS
The ACE inhibitors enalapril, captopril, and lisi-
nopril can cause scalded mouth or BMS. There is
improvement with reduction or discontinuation of the
medication [36].
Normal mucosal findings
Often regarded as asymptomatic variants of nor-
mal, multiple studies have shown geographic (Fig. 4),
fissured (Fig. 5), or scalloped tongues more frequently
in patients with tongue pain [2,15,37,38]. Although
the patient with oral pain and these findings techni-
cally does not fit under the rubric of BMS, the
connection between these oral findings and oral pain
has been documented and should be recognized.
These findings can also increase the patients fear of
cancer. The article on glossitis by Byrd et al elsewhere
in this issue addresses this topic in greater detail.
Evaluation and work-up of the patient with BMS
The many causes and multifactorial nature of
BMS make an organized approach to evaluation
important (Table 3). Diagnosis and treatment may
Fig. 4. Geographic tongue. The geographic tongue is a
combination of an atrophic tongue with a red base caused by
diminished filiform papillae (with resultant hypersensitivity)
and a furred tongue with a white base and hyperplasia of
filiform papillae. The geographic tongue may be sympto-
matic. (From Drage LA, Rogers RS III. Clinical assessment
and outcome in 70 patients with complaints of burning or
sore mouth symptoms. Mayo Clin Proc 1999;74:2238;
with permission.)
L.A. Drage, R.S. Rogers III / Dermatol Clin 21 (2003) 135145 139
be achieved best by a multidisciplinary approach
involving the dermatologist and the primary care
provider, dentist, psychiatrist, and otorhinolaryngol-
ogist. Simply treating the patient in a sympathetic
manner may improve the interaction and perhaps the
outcome [2,3,12].
Directed history concentrating on the medical,
dental, and psychologic or psychiatric history and
review of symptoms should occur. The description
of oral pain should include the following: duration;
character; level (scale of 1 to 10); site of involve-
ment; and subtype or pattern. Frank questions about
depression, anxiety, and fear of cancer should be
posed. Exacerbating factors, such as food and oral
preparations (mouthwash, gum, mints, toothpaste,
lip cosmetics, and smoking), should be elicited.
Relationship of pain to denture use, dental work,
and parafunctional oral behavior (tongue thrusting,
bruxism, or jaw clenching) should be documented.
All medications must be assessed for xerosto-
mic potential.
Physical examination with emphasis on a thor-
ough oral examination must be completed. Besides
identifying other diseases that could cause mouth
pain, this reassures the patient that cancer is not
present. Evaluation should include assessment for
erythema, glossitis, atrophy, candidiasis, geographic
tongue, lichen planus, and xerostomia. Clinicians with
knowledge and experience in the broad range and
presentation of oral disease are best equipped to
certify a truly normal oral mucosal examination.
Examination of dental work, dentures, denture func-
tion, and signs of parafunctional behavior may be
assessed best by a dental consultation.
Laboratory examination should include the per-
tinent tests in Table 2. Biopsy specimens are
unlikely to be beneficial if a normal clinical
examination is confirmed. Patch testing is espe-
cially important and fruitful in the patient with
Type 3 BMS and should include a standard series,
metal series, and oral flavorings and preservatives
(Box 1). The list of allergens is discussed in the
contribution by LeSueur and Yiannis elsewhere in
this issue.
Management
Burning mouth syndrome is a manageable prob-
lem with most patients responding to tailored therapy
(Box 2). Management should focus on controlling or
eliminating all potential causes of BMS, keeping in
mind that in many patients more than one factor
plays a role. Because of the number of conditions
causing oral pain, a single treatment protocol is not
appropriate. Treatment is tailored to the proposed
Table 3
Work-up of BMS
Thorough history and review of symptoms
Medications causing xerostomia
Dental or denture work
Oral care, oral products
Oral habits or parafunctional behavior
History of depression, anxiety, cancerphobia
Family history of oral cancer, psychiatric diagnoses, and
connective tissue disease
Oral examination
Erythema, candidiasis, xerostomia or other mucosal
abnormalities
Tongue disorders, such as a geographic, fissured, or
atrophic tongue
Dental work or dentures
Laboratory tests
Complete blood count
Iron, total iron binding capacity, iron saturation, ferritin
Vitamin B12, folate, zinc
Glucose, glycosylated hemoglobin
Culture for Candida
Patch testing
Include standard series, metal series, oral flavors and
preservatives
Further consultation if indicated by history and review
of systems
Psychometric testing and psychiatric consultation
Dentistry
Neurology
Otorhinolaryngology
Fig. 5. Fissured tongue. The fissured tongue is rare in
neonates and more common with age. About one sixth of
older patients have grooves and fissuring of the tongue
dorsum. Impaction of food and keratin debris can predispose
to inflammation and halitosis.
L.A. Drage, R.S. Rogers III / Dermatol Clin 21 (2003) 135145140
causes. Management plans for different scenarios
are reviewed.
Psychiatric disorders
A supportive environment is beneficial for con-
tinued treatment of the patient and may aid resolu-
tion of the symptoms in concert with other therapies
[2,3]. Psychiatric evaluation, medication, and psy-
chotherapy [39] may play a role in alleviating the
symptoms. Although optimally undertaken with the
guidance of a psychiatrist or psychologist; some
patients are resistant to psychiatric evaluation. Anti-
depressants and anxiolytics with less anticholinergic
impact (hence less xerostomia) are preferred. Sero-
tonin reuptake inhibitors typically cause less xero-
stomia and may be a good choice in this setting.
Reassurance that cancer is not present should be
stated clearly and repeatedly.
Denture or dental-related pain
Evaluation of dental work, dentures, denture
design faults, and parafunctional behavior by a spe-
cialist should be sought. Adaptation or replacement
may lead to relief of BMS. Removal of dentures at
night may be helpful. Avoidance of irritants, treat-
ment of dentures with anti-candidal agents, and a
review of dental hygiene should occur.
Deficiency syndromes
Replacement of iron, B12, folate, or zinc should
occur in patients with documented deficiencies. Grad-
ual improvement may follow. Evaluation into the
cause of the document deficiency must occur before
supplementation. Supplementation in absence of
documented deficiency is difficult to justify aside
from B vitamin replacement [20]. Lamey [3] recom-
mends empiric replacement of vitamins B1 (300 mg,
once a day) and vitamin B6 (50 mg, three times a day)
for 4 weeks.
Allergic contact stomatitis
Patch testing to dental and denture components,
metals, additives, preservatives, flavors and a stan-
dard series should occur under the supervision of a
dermatologist who is experienced in their proper use
and interpretation. The clinical correlation between
the patch test results and patient exposure history is
the most important component of the testing. Patient
education and training regarding the avoidance of
identified allergens is imperative.
Candidiasis
Because Candida is a normal part of the oro-
pharyngeal flora, a positive culture does not equate
to a pathologic process. Tests that quantitate Can-
dida infection are not available routinely. Typically,
empiric treatment for oral candidiasis is offered to
the patient with BMS and may benefit a subset of
patients. Treatment may include use of nystatin or
clotrimazole, which are available in multiple forms
including creams, rinses, and troche. One example
of an effective treatment regimen includes the use
of oral fluconazole, 100 mg Number 15: Day 1,
two pills; days 27, one pill; days 821, one pill
every other day. Dentures should also be treated for
Box 1. Patch testing in BMS
1. Standard series (The MayoClinic series includes 68 differentallergens)
2. Oral flavorings and preservatives3. Metal series
The allergens tested should include (butnot be limited to) the following:
Methyl methacrylateEthyl acrylateEthyleneglycol dimethacrylateTriethyleneglycol dimethacrylateBIS GMABenzoyl peroxidePropylene glycolSorbic acidBenzoic acidTartrazine yellowPeppermintSpearmintCinnamic aldehydeMentholFragrance mixBalsam of PeruCobalt chlorideNickel sulfateGold sodium thiosulfateAmalgamMercuric chlorideCadmium chloridePotassium dichromateFormaldehydep- Phenylenediamine
L.A. Drage, R.S. Rogers III / Dermatol Clin 21 (2003) 135145 141
candidiasis and dental hygiene reviewed. Dentures
should always be removed at night. Many patients
sleep with dentures in place all night. This predis-
poses to parafunctional habits and recurrent candi-
diasis (denture stomatitis).
Diabetes mellitus
All patients with BMS need to have diabetes
mellitus excluded with fasting blood glucose levels.
Patients with abnormal findings should be referred
for management and education. Control of diabetes
mellitus many lead to decrease in BMS. Change of
the diabetic medications can sometimes be helpful.
Some patients may need oral agents or some may
need insulin therapy.
Parafunctional habits
Once identified, management many include modi-
fication of denture design; behavioral therapy consist-
ing of habit monitoring, biofeedback, and relaxation
techniques [12]; and use of sugar-free chewing gum,
mouth guards, and even hypnotherapy.
Xerostomia
A number of general measures may be instituted
to counteract xerostomia (Box 3). The discontinua-
tion or substitution of medications with potential for
Box 2. Management strategies for BMS
Tenets of treatment:1. Focus on controlling or eliminating
all potential causes of BMS2. Tailor treatment for individual pa-
tient based on suspected causes3. Resort to empiric therapy only if
no cause of BMS is found or failureof treatment
Management plans may include thefollowing:
Psychiatric and psychologic disorder
Maintain supportive environmentPsychiatric evaluation and
managementAppropriate medication or
psychotherapyReassure cancer is not present
Denture or dental work
Evaluation by dentistAdaptation or replacement as needed
Deficiency syndromes
Document deficiencyEvaluate cause of deficiencyReplacement therapy
Allergic contact stomatitis
Referral to dermatologist with experi-ence in use and interpretation ofpatch tests
Patch test to standard, metal, oralpreservatives, flavor series
Clinical correlationPatient education in avoidance of iden-
tified allergen
Candidiasis
CultureTreatment with anti-candidiasis agents
Diabetes mellitus
Referral for management and education
Parafunctional behavior
Dental evaluation
Behavioral therapySugar-free chewing gum
Xerostomia
Discontinue medications thatcause xerostomia
General measuresSaliva substituteSialogogues
Idiopathic (empiric treatment)
Avoid irritantsTrial of treatment with
anti-candidal agentB-vitamin replacementDoxepin trialLow-dose tricyclic antidepressantsLocal clonazepamConsider referral to specialist in
oral medicine
L.A. Drage, R.S. Rogers III / Dermatol Clin 21 (2003) 135145142
causing xerostomia should be sought. Because xero-
stomia is a very common medication side effect,
sometimes a simple reduction in the number of
drugs used may improve xerostomia. Artificial sali-
va substitutes may be helpful. Sialogogues, such as
pilocarpine, are sometimes used [32]. Note the
contribution by Parks and Lancaster on oral mani-
festations of systemic disease elsewhere in this issue
for additional discussion of xerostomia and therapy
of the dry mouth.
Idiopathic
If no underlying cause for BMS is found or
treatment targeted to a proposed etiology is not
beneficial, treatment options may follow a more
empiric approach. This may include discontinuation
of irritating substances (alcohol-based mouthwashes,
cinnamon or mint products, and smoking); a trial
treatment with anti-candidal agents; and trial treat-
ment with B complex vitamins [3]. Doxepin, famil-
iar to many dermatologists, is often prescribed in
doses up to 75 mg for its antianxiety and antide-
pressant affects. At higher doses doxepin has a
greater potential for cardiac arrhythmia, xerostomia,
and full antidepressant effect and needs to be
carefully monitored
If no response is seen, tricyclic antidepressants
may be used in a chronic pain protocol manner
[2,5,26]. Typical doses include amitriptyline, 10 to
75 mg. Low doses of tricyclic antidepressants may
have an analgesic affect that is separate from their
action as antidepressants [33]. Use of benzodiaze-
pines [40,41] including systemic clonazepam [18]
have been reported to be effective in BMS.
Although the mechanism for their action may not
rely solely on their anxiolytic effect, concerns
regarding the chronic nature of BMS and the poten-
tial for abuse of this class of medication merits
cautious use. Interestingly, Woda et al [42] reported
benefit in 52% of patients treated with local applica-
tion of clonazepam (0.5 to 1 mg) two to three times
a day. They theorized that local application of
clonazepam acts locally to disrupt the neuropatho-
logic mechanism that underlies BMS. More unusual
treatments reported have included use of capsaicin
[43] and infrared laser [44].
Burning mouth syndrome is a treatable syndrome.
Treatment is associated with improvement in about
70% of patients [16] using a directed approach. If
that fails, an empiric approach is warranted. Spon-
taneous remissions have also been noted to occur
[45,46].
Summary
Burning mouth syndrome is the occurrence of oral
pain in a patient with a normal oral mucosal exam-
ination. It can be caused by both organic and psycho-
logic or psychiatric factors, which can be broken
down into local, systemic, psychologic or psychiatric,
and idiopathic causes. The most frequently associated
conditions are psychiatric (depression, anxiety, or
cancerphobia); xerostomia; nutritional deficiency;
allergic contact dermatitis; candidiasis; denture-
related pain; and parafunctional behavior. Multiple
different factors contributing to the oral pain are
common, and a systematic approach to the evaluation
is important.
Identification of correctable causes of BMS should
be emphasized and psychiatric causes should not be
invoked without thorough evaluation of the patient. A
Box 3. Xerostomia management
General measures include the following:
Review medications and replacethose with known xerostomic po-tential. Discontinue unnecessarymedications.
Increase water intake throughoutthe day
Use humidifier in bedroomAvoid alcohol and alcohol-containing
mouthwashAvoid caffeineUse sugar-free candy, gum, and
beveragesUse petroleum jelly on lips before bed
and throughout dayFrequent dental examination. Patients
with xerostomia have increased riskof cavities and gum disease.
Commercial saliva substitutes: use asoften as needed and before bed;available without a prescription.
Examples include the following:
Mouth Kote (spray)Moi-stir-spray and swabsOptimoist (spray)
SialogoguePilocarpine, 5 mg tidCivemeline, 30 mg tid
L.A. Drage, R.S. Rogers III / Dermatol Clin 21 (2003) 135145 143
directed history and careful oral examination must be
completed to exclude local diseases and identify clues
to potential causes. Assessment of medications, psy-
chiatric history and background, and selected labora-
tory and patch tests may help identify the etiologies of
these symptoms.
Treatment should be tailored to each patient and
may best be managed in a multidisciplinary approach
with input from dermatologists, dentists, psychiatrists,
otorhinolaryngologists, and primary care providers. A
thoughtful and structured evaluation of the patient
with BMS has been associated with improvement in
about 70% of patients. The remaining patients may
benefit from empiric therapy with a chronic pain pro-
tocol and continued supportive interactions.
References
[1] Basker RM, Sturdee DW, Davenport JC. Patients with
burning mouths: a clinical investigation of causative
factors, including the climacteric and diabetes. Br
Dent J 1978;145:916.
[2] Drage LA, Rogers III RS. Clinical assessment and out-
come in 70 patients with complaints of burning or sore
mouth symptoms. Mayo Clin Proc 1999;74:2238.
[3] Lamey PJ. Burning mouth syndrome: approach to suc-
cessful management. Dent Update 1998;25:298300.
[4] Lamey PJ. Burning mouth syndrome. Dermatol Clin
1996;14:33954.
[5] Lamey PJ, Lamb AB. Prospective study of aetiological
factors in burning mouth syndrome. BMJ 1988;296:
12436.
[6] Main DM, Basker RM. Patients complaining of a burn-
ing mouth: further experience in clinical assessment
and management. Br Dent J 1983;154:20611.
[7] Grushka M, Sessle BJ, Miller R. Pain and personality
profiles in burning mouth syndrome. Pain 1987;28:
15567.
[8] Grushka M. Clinical features of burning mouth syn-
drome. Oral Surg Oral Med Oral Pathol Oral Radiol
Endod 1987;63:306.
[9] Bergdahl M, Bergdahl J. Burning mouth syndrome:
prevalence and associated factors. J Oral Pathol Med
1999;28:3504.
[10] Ferguson MM, Carter J, Boyle P, et al. Oral complaints
related to climacteric symptoms in oophorectomized
women. J R Soc Med 1981;74:4928.
[11] Browning S, Hislop S, Scully C, et al. The association
between burning mouth syndrome and psychosocial
disorders. Oral Surg Oral Med Oral Pathol Oral Radiol
Endod 1987;64:1714.
[12] Tourne LP, Fricton JR. Burning mouth syndrome: crit-
ical review and proposed clinical management. Oral
Surg Oral Med Oral Pathol Oral Radiol Endod 1992;
74:15867.
[13] Lamey PJ, Lamb AB, Hughes A, et al. Type 3 burning
mouth syndrome: psychological and allergic aspects.
J Oral Pathol Med 1994;23:2169.
[14] Lamb AB, Lamey PJ, Reeve PE. Burning mouth syn-
drome: psychological aspects. Br Dent J 1988;165:
25660.
[15] Zegarelli DJ. Burning mouth: an analysis of 57 pa-
tients. Oral Surg Oral Med Oral Pathol Oral Radiol
Endod 1984;58:348.
[16] Bogetto F, Maina G, Ferro G, et al. Psychiatric comor-
bidity in patients with burning mouth syndrome. Psy-
chosom Med 1998;60:37885.
[17] Grinspan D, Blanco FG, Allevato MA, et al. Burning
mouth syndrome. Int J Dermatol 1995;34:4837.
[18] Grushka M, Epstein J, Mott A. An open-label, dose
escalation pilot study of the effect of clonazepam in
burning mouth syndrome. Oral Surg Oral Med Oral
Pathol Oral Radiol Endod 1998;86:55761.
[19] Haneke E. Burning mouth syndrome. In: Burgdorf
WHC, Katz SB, editors. Dermatology: progress and
perspectives. New York: Parthenon Publishing; 1993.
p. 5845.
[20] Lamey PJ, Allam BF. Vitamin status of patients with
burning mouth syndrome and the response to replace-
ment therapy. Br Dent J 1986;160:814.
[21] Lamey PJ, Lewis MA. Oral medicine in practice: burn-
ing mouth syndrome. Br Dent J 1989;167:197200.
[22] Maresky LS, van der Bijl P, Gird I. Burning mouth
syndrome: evaluation of multiple variables among 85
patients. Oral Surg Oral Med Oral Pathol Oral Radiol
Endod 1993;75:3037.
[23] Rojo L, Silvestre FJ, Bagan JV, et al. Psychiatric mor-
bidity in burning mouth syndrome: psychiatric inter-
view versus depression and anxiety scales. Oral Surg
Oral Med Oral Pathol Oral Radiol Endod 1993;75:
30811.
[24] van der Ploeg HM, van der Waal N, Eijkman MAJ, et
al. Psychological aspects of patients with burning
mouth syndrome. Oral Surg Oral Med Oral Pathol Oral
Radiol Endod 1987;63:6648.
[25] van der Waal I. The burning mouth syndrome. Copen-
hagen: Munksgaard; 1990.
[26] Grushka M. Burning mouth syndrome. Dent Clin
North Am 1991;35:17184.
[27] Schmitt RJ, Sheridan PJ, Rogers III RS. Pernicious
anemia with associated glossodynia. J Am Dent Assoc
1988;117:83840.
[28] Dutree-Meulenberg ROGM, Kozel MMA, van Joost
Th. Burning mouth syndrome: a possible etiologic role
for local contact hypersensitivity. J Am Acad Dermatol
1992;26:93540.
[29] Kaaber S, Thulin H, Nielsen E. Skin sensitivity to
denture base materials in the burning mouth syndrome.
Contact Dermatitis 1979;5:906.
[30] van Joost TH, van Ulsen J, van Loon LAJ. Contact
allergy to denture materials in the burning mouth syn-
drome. Contact Dermatitis 1988;18:979.
[31] Helton J, Storrs F. The burning mouth syndrome: lack
of a role for contact urticaria and contact dermatitis.
J Am Acad Dermatol 1994;31:2015.
L.A. Drage, R.S. Rogers III / Dermatol Clin 21 (2003) 135145144
[32] Osaki T, Yoneda K, Yamamoto T, et al. Candidiasis
may induce glossodynia without objective manifesta-
tion. Am J Med Sci 2000;319:1005.
[33] Mott AE, Grushka M, Sessle BJ. Diagnosis and man-
agement of taste disorders and burning mouth syn-
drome. Dent Clin North Am 1993;37:3371.
[34] Wardrop RW, Hailes J, Burger H, et al. Oral discomfort
at menopause. Oral Surg Oral Med Oral Pathol Oral
Radiol Endod 1989;67:53540.
[35] Pisanty S, Rafaely B, Polishuk WZ. The effect of ste-
roid hormones on buccal mucosa of menopausal wom-
en. Oral Surg Oral Med Oral Pathol Oral Radiol Endod
1975;40:34653.
[36] Savino LB, Haushalter NM. Lisinopril induced
scalded mouth syndrome. Pharmacol Ther 1992;26:
13812.
[37] Gorsky M, Silverman Jr S, Chinn H. Burning mouth
syndrome: a review of 98 cases. J Oral Med 1987;42:
79.
[38] Powell FC. Glossodynia and other disorders of the
tongue. Dermatol Clin 1987;5:68793.
[39] Bergdahl J, Anneroth G. Burning mouth syndrome:
literature review and model for research and manage-
ment. J Oral Pathol Med 1993;22:4338.
[40] Gorsky M, Silverman Jr S, Chinn H. Clinical charac-
teristics and management outcome in the burning
mouth syndrome: an open study of 130 patients. Oral
Surg Oral Med Oral Pathol Oral Radiol Endod
1991;72:1925.
[41] Huang W, Rothe MJ, Grant-Kels JM. The burning
mouth syndrome. J Am Acad Dermatol 1996;34:918.
[42] Woda A, Navez ML, Picard P, et al. A possible ther-
apeutic solution for stomatodynia (burning mouth syn-
drome). J Orofacial Pain 1998;12:2728.
[43] Epstein JB, Marcoe JH. Topical application of capsai-
cin for treatment of oral neuropathic pain and trigemi-
nal neuralgia. Oral Surg Oral Path 1994;77:13540.
[44] Cekic-Arambasin A, Durdevic-Matricc A, Mravak-
Stipetic M, et al. Use of soft laser in the treatment of
oral symptoms. Acta Stomatol Croat 1990;24:2818.
[45] Gilpin SF. Glossodynia. JAMA 1936;106:17224.
[46] Grushka M, Katz RL, Sessle BJ. Spontaneous remis-
sion in burning mouth syndrome (BMS) [abstract].
J Dent Res 1986;66:274.
L.A. Drage, R.S. Rogers III / Dermatol Clin 21 (2003) 135145 145