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LESIONS OF ORAL
CAVITY
DR JOEL G. MATHEW
ULCERS OF ORAL CAVITY
 INFECTIONS
 VIRAL-HERPANGINA, HERPES SIMPLEX
 BACTERIAL-Vincent’s infection, TB, syphilis
 Fungal: Candidiasis
 Immune disorders: Aphthous ulcer, Behcet’s syndrome
 Trauma
 ill-fitting denture, phenol, aspirin burns, Hot food
 Neoplasms
 Skin disorders: Erythema multiforme, lichen planus, BMMP, bullous
pemphigoid, lupus erythematosus
 Blood disorders: Leukaemia, agranulocytosis, pancytopenia
 Drug allergy: Mouth washes, tooth paste, etc.
Reactions to systemic drugs
 Vitamin deficiencies
 Miscellaneous: Radiation mucositis, cancer chemotherapy, diabetes
mellitus, uraemia
INFECTIONS
HERPANGINA
 SYN: Vesicular stomatitis , Acute
lymphonodular pharyngitis
 Cause: Enteroviruses-Coxsackie A, EV 71
 Characteristic vesicular rash on tonsillar pillars,
soft palate, uvula, tonsils, posterior pharyngeal
wall
 Discrete 1- to 2-mm vesicles and ulcers
 Enlarge over 2-3 days to 3-4 mm and are
surrounded by erythematous rings up to 10 mm
 1-15 lesions are present, usually around 5
 Usually resolve without complications
 Rarely, meningitis
Herpetic gingivostomatitis
 Syn: orolabial herpes
 Cause: HSV
 Primary
 Children
 Clusters of multiple vesicles -> ulcers
 Fever, malaise and headache , sore throat and
lymphadenopathy.
 Secondary
 Adults, mild
 Vermilion border of the lip > hard palate and gingiva
 Reactivation of dormant virus in trigeminal ganglion
 Acyclovir, 200 mg, five times a day for 5 days to reduce
viral load
Hand, foot and mouth disease
 Cause: Coxsackievirus A16 and enterovirus 71 (EV71)
 spread via the fecal-oral and perhaps respiratory
routes
 primarily in children
 vesicular palmoplantar eruption and erosive
stomatitis.
 Cloudy vesicles with a red halo are highly
characteristic of this disease.
Vincent’s infection
 Syn: acute necrotising ulcerative gingivitis, trench
mouth
 Causative organisms include a fusiform bacillus and a
spirochaete –borrelia vincentii
 Affects young adults and middle-aged persons
 Starts at the interdental papillae -> free margins of the
gingivae
 Lesions covered with necrotic slough.
 Gingivae become red and oedematous.
 Similar ulcer and necrotic membrane may also form
over the tonsil (vincent’s angina).
 Diagnosis: smear from the affected area.
 Treatment is
 Systemic antibiotics (penicillin or erythromycin and
metronidazole),
 Frequent mouth washes (with sodium bicarbonate
solution) and attention to dental hygiene.
Moniliasis (candidiasis)
 caused by Candida albicans
 Thrush
 white grey patches on the oral mucosa and
tongue.
 infants and children
 systemic malignancy and diabetes or taking
broad spectrum antibiotics, cytotoxic drugs,
steroids or radiation.
 Thrush can be treated by topical application of
nystatin or clotrimazole.
 Chronic hypertrophic candidiasis. Also called candidal leukoplakia.
 White patch which cannot be wiped off.
 Mostly affects anterior buccal mucosa just behind the angle of mouth.
 Hypertrophic form usually requires excisional surgery.
IMMUNE DISORDERS
Aphthous ulcers
 Recurrent and superficial
 Aetiology: Unknown. Autoimmune, Nutritional
(Folate, B12, Iron), Viral, Bacterial, Food
allergies, Hormonal, Stress
 usually involving movable mucosa, i.e. inner
surfaces of lips, buccal mucosa, tongue, floor
of mouth and soft palate, sparing mucosa of
the hard palate and gingivae.
 Minor form
 more common,
 ulcers are 2–10 mm in size and multiple with a
central necrotic area and a red
 They heal in about 2 weeks without leaving a
scar.
 Major form, ulcer is very big, 2–4 cm in size,
and heals with a scar but is soon followed by
another ulcer.
 Topical application of steroids
 Cauterisation with 10% silver nitrate.
 In severe cases, 250 mg of tetracycline dissolved in 50 ml of water is
given as mouth rinse and then to be swallowed, four times a day.
 Local pain can be relieved with lignocaine viscous.
Behcet’s syndrome (Oculo-oro-
genital syndrome)
 Behçet's disease is a complex multisystem disease characterized by
oral and genital ulcers and other systemic features.
 Diagnosis is based on the International Criteria for Behçet's Disease
including:
 oral aphthae,
 genital aphthae,
 ocular lesions,
 cutaneous lesions,
 and a positive pathergy test.
 Cutaneous lesions should display a neutrophilic vascular reaction on
histopathologic examination.
 Seen worldwide, with the highest prevalence reported in Turkey and
Japan
 prevalence and often the severity is increased in the Middle East
and the Mediterranean
 predominantly affect males
 Cause and Pathogenesis
 Heredity, immunologic factors, infectious agents, inflammatory
mediators, and clotting factors likely contribute.
 Oral aphthae, or Canker sores are often the initial
feature of Behçet's disease and constitute a requisite
diagnostic feature
 usually occur in crops of more than 3 to 10s
 painful and shallow, and they heal without scarring
over 1 to 3 weeks
 Genital ulcers typically occur on the scrotum and penis
in males and on the vulva or vaginal mucosa in
females.
 These aphthae are similar in appearance to oral
lesions, but they have a greater tendency to scar and
may recur less frequently.[
 Cutaneous-
 erythema nodosum–like lesions,
 pyoderma gangrenosum–like lesions,
 Sweet's syndrome–like lesions,
 cutaneous small vessel vasculitis, and pustular vasculitic
lesions including lesions induced by trauma—the so-called
pathergy lesion.
 Pathergy signifies the development of erythematous
pustules or papules 24 to 48 hours following puncture of
the skin with a 20- to 21-gauge sterile needle.
 Specimens from all these lesions demonstrate a
neutrophilic vascular reaction on histopathologic
analysis.
 Ophthalmic (83% to 95% of men and 67% to 73% of
women)
 anterior and posterior uveitis,
 retinal vasculitis, and hypopyon, with secondary
glaucoma,
 cataract formation, decreased visual acuity, and
synechiae formation
 Arthritis of Behçet's disease is typically a nonerosive, inflammatory,
symmetric, or asymmetric oligoarthritis
 Central nervous system (CNS) involvement is most commonly
characterized by
 brain stem or corticospinal tract syndromes (neuro-Behçet's syndrome),
 venous sinus thrombosis,
 increased intracranial pressure
 isolated headache.
 Cardiac complications include
 myocardial infarction,
 pericarditis,
 arterial and venous thromboses, and
 aneurysm formation.
Miscellaneous lesions of oral cavity
and tongue
 Median rhomboid glossitis
 red rhomboid area, devoid of papillae, seen
on the dorsum of tongue in front of foramen
caecum.
 Due to chronic oral candidiasis
TRAUMATIC ULCER
 lateral border of tongue -jagged tooth or ill-fitting
denture;
 buccal mucosa -cheek bite;
 palate - injury with a foreign object such as pencil
or tooth brush
 acute ulcerative lesions of oral and
oropharyngeal mucosa - ingestion of acids or
alkalies or hot fluids.
 Aspirin burn - buccal sulcus
SKIN DISORDERS
Erythema multiforme
 Acute, self-limited, polymorphous eruption
 Symmetrically distributed macules, papules, and bullae, with
an edematous, petechial, vesicular, or bullous dusky violet
center.
 It is probably due to cell-mediated hypersensitivity reaction
to certain drugs or infections, particularly in genetically
predisposed individuals, those immunocompromised or with
autoimmune disease.
 Mucosal lesions are ocular (conjunctivitis, keratitis), oral
(stomatitis, cheilitis), nasal, pharyngeal, tracheal, and genital
(balanitis and valvulitis).
 Dull red, flat or slightly raised maculopapules, which may
remain small or may increase in size to reach a diameter of 1-
3 cm in 48 h. Typical cases show at least some target (or iris)
lesions.
 The disease is self-limiting and management is mainly
supportive. Steroids are used to treat the severe form.
Pemphigus vulgaris
 autoimmune disorder affecting older age group (50–70) [AMBD]
 Oral ulcerations are superficial and involve palate, buccal mucosa and
tongue.
 Jagged intraoral erosions->Blisters
 Treatment consists of systemic steroids and cytotoxic drugs.
Benign mucous membrane
pemphigoid (BMMP)
 Most common AMBD
 autoimmune disorder.
 Mucosal lesions involve cheek,
gingivae and palate > Conjunctiva
 Bulla filled with clear or haemorrhagic
fluid -> ruptures to form superficial
ulceration covered with shaggy
collapsed mucosa.
 Skin lesions may be absent.
 Treatment consists of steroids.
Lichen planus
 Oral lichen planus (OLP) can occur without
cutaneous disease.
 Onset before middle age is rare; the mean age of
onset is in the sixth decade.
 Women outnumber men by more than 2:1.
 Mucous membrane involvement is observed in
more than 50% of patients with cutaneous lichen
planus
 The most common location of OLP is the buccal
mucosa (80% to 90%) followed by the tongue (30%
to 50%)
Lavy white lesions on buccal mucosa
Geographic tongue
 Also called benign migratory glossitis,
 Well-defined areas of atrophied filiform
papillae bordered by arcs of normal or
hyperplastic filiform papillae and by
gradual changes in the location of these
lesions over time
Submucous Fibrosis
 Definition:
 Submucous fibrosis represents a multifactorial disorder;
 with the considered chief etiologic factor being the consistent and habitual use
of areca (betel) nut, either in the form of chewing or simply placing a quid of
material (paan masala) in the buccal or labial sulcus several time per day, or in
a packaged powdered form with other components (guthka), over many years.
 premalignant condition with transformation rates as high as 7.6%
 Etiology and pathogenesis:
 failure of collagen remodeling
 altered epithelial-mesenchymal interactions ->formation of collagenous bands
and aggregates within the submucosa and lamina propria.
 diminished level of functional collagenase levels
 Clinical Features
 Changes of submucous fibrosis are most marked
over soft palate, faucial pillars and buccal mucosa
 Initial mucosal alterations: erythema with or without
vesiculation.
 Later: slow diminishment of erythema and a
progressive decrease in the degree of oral opening
and tongue mobility
 Pallor of the normally pink mucosa becomes
evident as the underlying chronic inflammation
recedes and fibrosis and hyalinization progress.
 Scar bands may become evident deep within the
buccal soft tissues, further limiting jaw opening and
function.
 Development of squamous cell carcinoma is
characterized by a gradual thickening of the
epithelial surface with hyperplastic to verrucous
surface qualities becoming evident.
 Histology:
 juxtaposition of atrophic epithelium
surfacing a subjacent fibrosis.
 Early connective tissue alterations
are characterized by delicate and
loosely arranged collagen fibers with
progressive degrees of hyalinization
 In the late stages:
 complete hyalinization of the
supportive connective tissue.
 Variable degrees of chronic
inflammation occur in the form
of lymphocytes and plasma
cells.
 Variable levels of dysplasia have
been noted.
 Management of oral submucous fibrosis is problematic, particularly in advanced
cases and when the use of areca-containing products remains in place.
 Medical:
 Avoid irritant factors
 Topical injection of steroids-Dexamethasone
 Treat existent anaemia or vitamin deficiencies
 Encourage jaw opening exercises.
 Surgical
 Surgical release procedures of scar bands have been only modestly successful.
 More recently collagenase and pentoxifylline administration in separate studies
has been proposed

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Lesions of oral cavity

  • 1. LESIONS OF ORAL CAVITY DR JOEL G. MATHEW
  • 2. ULCERS OF ORAL CAVITY  INFECTIONS  VIRAL-HERPANGINA, HERPES SIMPLEX  BACTERIAL-Vincent’s infection, TB, syphilis  Fungal: Candidiasis  Immune disorders: Aphthous ulcer, Behcet’s syndrome  Trauma  ill-fitting denture, phenol, aspirin burns, Hot food  Neoplasms  Skin disorders: Erythema multiforme, lichen planus, BMMP, bullous pemphigoid, lupus erythematosus
  • 3.  Blood disorders: Leukaemia, agranulocytosis, pancytopenia  Drug allergy: Mouth washes, tooth paste, etc. Reactions to systemic drugs  Vitamin deficiencies  Miscellaneous: Radiation mucositis, cancer chemotherapy, diabetes mellitus, uraemia
  • 5. HERPANGINA  SYN: Vesicular stomatitis , Acute lymphonodular pharyngitis  Cause: Enteroviruses-Coxsackie A, EV 71  Characteristic vesicular rash on tonsillar pillars, soft palate, uvula, tonsils, posterior pharyngeal wall  Discrete 1- to 2-mm vesicles and ulcers  Enlarge over 2-3 days to 3-4 mm and are surrounded by erythematous rings up to 10 mm  1-15 lesions are present, usually around 5  Usually resolve without complications  Rarely, meningitis
  • 6. Herpetic gingivostomatitis  Syn: orolabial herpes  Cause: HSV  Primary  Children  Clusters of multiple vesicles -> ulcers  Fever, malaise and headache , sore throat and lymphadenopathy.  Secondary  Adults, mild  Vermilion border of the lip > hard palate and gingiva  Reactivation of dormant virus in trigeminal ganglion  Acyclovir, 200 mg, five times a day for 5 days to reduce viral load
  • 7. Hand, foot and mouth disease  Cause: Coxsackievirus A16 and enterovirus 71 (EV71)  spread via the fecal-oral and perhaps respiratory routes  primarily in children  vesicular palmoplantar eruption and erosive stomatitis.  Cloudy vesicles with a red halo are highly characteristic of this disease.
  • 8. Vincent’s infection  Syn: acute necrotising ulcerative gingivitis, trench mouth  Causative organisms include a fusiform bacillus and a spirochaete –borrelia vincentii  Affects young adults and middle-aged persons  Starts at the interdental papillae -> free margins of the gingivae  Lesions covered with necrotic slough.  Gingivae become red and oedematous.  Similar ulcer and necrotic membrane may also form over the tonsil (vincent’s angina).  Diagnosis: smear from the affected area.  Treatment is  Systemic antibiotics (penicillin or erythromycin and metronidazole),  Frequent mouth washes (with sodium bicarbonate solution) and attention to dental hygiene.
  • 9. Moniliasis (candidiasis)  caused by Candida albicans  Thrush  white grey patches on the oral mucosa and tongue.  infants and children  systemic malignancy and diabetes or taking broad spectrum antibiotics, cytotoxic drugs, steroids or radiation.  Thrush can be treated by topical application of nystatin or clotrimazole.
  • 10.  Chronic hypertrophic candidiasis. Also called candidal leukoplakia.  White patch which cannot be wiped off.  Mostly affects anterior buccal mucosa just behind the angle of mouth.  Hypertrophic form usually requires excisional surgery.
  • 12. Aphthous ulcers  Recurrent and superficial  Aetiology: Unknown. Autoimmune, Nutritional (Folate, B12, Iron), Viral, Bacterial, Food allergies, Hormonal, Stress  usually involving movable mucosa, i.e. inner surfaces of lips, buccal mucosa, tongue, floor of mouth and soft palate, sparing mucosa of the hard palate and gingivae.  Minor form  more common,  ulcers are 2–10 mm in size and multiple with a central necrotic area and a red  They heal in about 2 weeks without leaving a scar.  Major form, ulcer is very big, 2–4 cm in size, and heals with a scar but is soon followed by another ulcer.
  • 13.  Topical application of steroids  Cauterisation with 10% silver nitrate.  In severe cases, 250 mg of tetracycline dissolved in 50 ml of water is given as mouth rinse and then to be swallowed, four times a day.  Local pain can be relieved with lignocaine viscous.
  • 14. Behcet’s syndrome (Oculo-oro- genital syndrome)  Behçet's disease is a complex multisystem disease characterized by oral and genital ulcers and other systemic features.  Diagnosis is based on the International Criteria for Behçet's Disease including:  oral aphthae,  genital aphthae,  ocular lesions,  cutaneous lesions,  and a positive pathergy test.  Cutaneous lesions should display a neutrophilic vascular reaction on histopathologic examination.
  • 15.  Seen worldwide, with the highest prevalence reported in Turkey and Japan  prevalence and often the severity is increased in the Middle East and the Mediterranean  predominantly affect males  Cause and Pathogenesis  Heredity, immunologic factors, infectious agents, inflammatory mediators, and clotting factors likely contribute.
  • 16.  Oral aphthae, or Canker sores are often the initial feature of Behçet's disease and constitute a requisite diagnostic feature  usually occur in crops of more than 3 to 10s  painful and shallow, and they heal without scarring over 1 to 3 weeks  Genital ulcers typically occur on the scrotum and penis in males and on the vulva or vaginal mucosa in females.  These aphthae are similar in appearance to oral lesions, but they have a greater tendency to scar and may recur less frequently.[
  • 17.  Cutaneous-  erythema nodosum–like lesions,  pyoderma gangrenosum–like lesions,  Sweet's syndrome–like lesions,  cutaneous small vessel vasculitis, and pustular vasculitic lesions including lesions induced by trauma—the so-called pathergy lesion.  Pathergy signifies the development of erythematous pustules or papules 24 to 48 hours following puncture of the skin with a 20- to 21-gauge sterile needle.  Specimens from all these lesions demonstrate a neutrophilic vascular reaction on histopathologic analysis.  Ophthalmic (83% to 95% of men and 67% to 73% of women)  anterior and posterior uveitis,  retinal vasculitis, and hypopyon, with secondary glaucoma,  cataract formation, decreased visual acuity, and synechiae formation
  • 18.  Arthritis of Behçet's disease is typically a nonerosive, inflammatory, symmetric, or asymmetric oligoarthritis  Central nervous system (CNS) involvement is most commonly characterized by  brain stem or corticospinal tract syndromes (neuro-Behçet's syndrome),  venous sinus thrombosis,  increased intracranial pressure  isolated headache.  Cardiac complications include  myocardial infarction,  pericarditis,  arterial and venous thromboses, and  aneurysm formation.
  • 19. Miscellaneous lesions of oral cavity and tongue  Median rhomboid glossitis  red rhomboid area, devoid of papillae, seen on the dorsum of tongue in front of foramen caecum.  Due to chronic oral candidiasis
  • 20. TRAUMATIC ULCER  lateral border of tongue -jagged tooth or ill-fitting denture;  buccal mucosa -cheek bite;  palate - injury with a foreign object such as pencil or tooth brush  acute ulcerative lesions of oral and oropharyngeal mucosa - ingestion of acids or alkalies or hot fluids.  Aspirin burn - buccal sulcus
  • 22. Erythema multiforme  Acute, self-limited, polymorphous eruption  Symmetrically distributed macules, papules, and bullae, with an edematous, petechial, vesicular, or bullous dusky violet center.  It is probably due to cell-mediated hypersensitivity reaction to certain drugs or infections, particularly in genetically predisposed individuals, those immunocompromised or with autoimmune disease.  Mucosal lesions are ocular (conjunctivitis, keratitis), oral (stomatitis, cheilitis), nasal, pharyngeal, tracheal, and genital (balanitis and valvulitis).  Dull red, flat or slightly raised maculopapules, which may remain small or may increase in size to reach a diameter of 1- 3 cm in 48 h. Typical cases show at least some target (or iris) lesions.  The disease is self-limiting and management is mainly supportive. Steroids are used to treat the severe form.
  • 23. Pemphigus vulgaris  autoimmune disorder affecting older age group (50–70) [AMBD]  Oral ulcerations are superficial and involve palate, buccal mucosa and tongue.  Jagged intraoral erosions->Blisters  Treatment consists of systemic steroids and cytotoxic drugs.
  • 24. Benign mucous membrane pemphigoid (BMMP)  Most common AMBD  autoimmune disorder.  Mucosal lesions involve cheek, gingivae and palate > Conjunctiva  Bulla filled with clear or haemorrhagic fluid -> ruptures to form superficial ulceration covered with shaggy collapsed mucosa.  Skin lesions may be absent.  Treatment consists of steroids.
  • 25. Lichen planus  Oral lichen planus (OLP) can occur without cutaneous disease.  Onset before middle age is rare; the mean age of onset is in the sixth decade.  Women outnumber men by more than 2:1.  Mucous membrane involvement is observed in more than 50% of patients with cutaneous lichen planus  The most common location of OLP is the buccal mucosa (80% to 90%) followed by the tongue (30% to 50%) Lavy white lesions on buccal mucosa
  • 26. Geographic tongue  Also called benign migratory glossitis,  Well-defined areas of atrophied filiform papillae bordered by arcs of normal or hyperplastic filiform papillae and by gradual changes in the location of these lesions over time
  • 27. Submucous Fibrosis  Definition:  Submucous fibrosis represents a multifactorial disorder;  with the considered chief etiologic factor being the consistent and habitual use of areca (betel) nut, either in the form of chewing or simply placing a quid of material (paan masala) in the buccal or labial sulcus several time per day, or in a packaged powdered form with other components (guthka), over many years.  premalignant condition with transformation rates as high as 7.6%  Etiology and pathogenesis:  failure of collagen remodeling  altered epithelial-mesenchymal interactions ->formation of collagenous bands and aggregates within the submucosa and lamina propria.  diminished level of functional collagenase levels
  • 28.  Clinical Features  Changes of submucous fibrosis are most marked over soft palate, faucial pillars and buccal mucosa  Initial mucosal alterations: erythema with or without vesiculation.  Later: slow diminishment of erythema and a progressive decrease in the degree of oral opening and tongue mobility  Pallor of the normally pink mucosa becomes evident as the underlying chronic inflammation recedes and fibrosis and hyalinization progress.  Scar bands may become evident deep within the buccal soft tissues, further limiting jaw opening and function.  Development of squamous cell carcinoma is characterized by a gradual thickening of the epithelial surface with hyperplastic to verrucous surface qualities becoming evident.
  • 29.  Histology:  juxtaposition of atrophic epithelium surfacing a subjacent fibrosis.  Early connective tissue alterations are characterized by delicate and loosely arranged collagen fibers with progressive degrees of hyalinization  In the late stages:  complete hyalinization of the supportive connective tissue.  Variable degrees of chronic inflammation occur in the form of lymphocytes and plasma cells.  Variable levels of dysplasia have been noted.
  • 30.  Management of oral submucous fibrosis is problematic, particularly in advanced cases and when the use of areca-containing products remains in place.  Medical:  Avoid irritant factors  Topical injection of steroids-Dexamethasone  Treat existent anaemia or vitamin deficiencies  Encourage jaw opening exercises.  Surgical  Surgical release procedures of scar bands have been only modestly successful.  More recently collagenase and pentoxifylline administration in separate studies has been proposed