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ORAL LICHEN
PLANUS
ARSALAN WAHID MALIK
Oral Lichen Planus
Common mucocutaneous disease with varying
clinical presentation
Premalignant condition
Involvement of oral mucosa is frequent along
with or preceded by lesions on skin and genital
mucous membrane
Definition
 OLP is a rather common chronic mucocutaneous
disease which probably arises due to abnormal
immunological reaction and the disease have some
tendency to undergo malignant transformation
Lichenoid reactions
 Exhibits clinical and histological similarity
 Distinguished from OLP on the basis of
1. Association with administration of drug,
contact with a metal,
use of food flavors or systemic diseases
2. Resolution when the cause is eliminated or
when disease is treated
Epidemiology
 Very common- 1% of population
 In asians 1.5%(average)
3.7% mixed oral habits
0.3% non users of tobacco
 Risk more among who smoke and chew
tobacco
cutaneous lesion alone 35%
mucosal lesion alone 25%
both together 40%
Etiology
 Specific etiology is unknown
 Psychological stress
 No evident genetic base or no uniform etiologic factors
 Abnormal recognition and expression of basal
keratinocytes of epithelium as foreign antigens by
langerhans cells
Pathogenesis
CD8 + T cells trigger the apoptosis of oral
epithelial cells
They recognize an antigen which is similar to an
antigen associated with major histocompatability
complex class 1 on keratinocytes
They release cytokines that attract additional
lymphocytes which accumulate in sub basilar
connective tissue
Liquefaction degeneration of basal keratinocytes
Clinical Features
 Middle aged or elderly people
mean age of onset- 5th
decade of life
rarely in young adults and children
 More in females ( 1.4:1 )
Site- Both skin lesions and mucosal lesions are present
Skin Lesions
 Purple, pruritic and polygonal papules
 May be discreet or gradually coalesce into plaques
each covered by fine glistering scale
 Bilaterally symmetrical
 Increase in size if subjected to any irritation
 Usually self limiting unlike the oral lesions lasting only
one year or less
Skin Lesions
 Initially red > purple or violaceous hue > a dirty
brownish color
 Periods of regression and recurrence
 “Koebner’s phenomenon”- skin lesions extend along
the areas of injury or irritation
 Most often on wrist, forearms, knees, thighs and trunk
 Face remains uninvolved
Mucosal Lesions
 Normally asymptomatic
 Bilaterally symmetrical
 Sometimes simultaneously have OSF, leukoplakia,etc.
 Clinical types
1.reticular
2.atrophic
3.erosive
4.bullous
5. other types
Reticular type
 Most common and most readily recognized
form
 Slightly elevated fine whitish lines
(Wickham’s striae) in lace like or annular
pattern
 Lines are wavy and parallel
 A tiny elevated dot like structure at the point
of intersection of lines
 Commonly on buccal mucosa and buccal
vestibule
Atrophic type
 Keratotic changes
combined with mucosal
erythema
 smooth, poorly defined
erythematus areas with or
without peripheral striae
 Usually associated with
desquamative gingivitis
 Pain and burning
sensation
Erosive type
 Pseudo membrane covered ulcerations with
keratosis and erythema
 Severe form with extensive degeneration and
separation of epithelium from connective
tissue
 Pain, burning sensation, bleeding,
desquamative gingivitis
 Commonly on buccal mucosa and vestibule
 More dysplasia and malignant transformation
Bullous type
 Vesciculobullous presentation combined
with reticular or erosive pattern
 Rare form characterized by large vesicles
or bullae (4mm to 2cm)
 Lesions usually develop within an
erythematus base, rupture immediately
leaving painful ulcers
 Usually have peripheral radiating striae and
seen on posterior part of buccal mucosa
Other types
 Plaque type: flattened white areas
-dorsal surface of tongue
-often resemble leukoplakia
 Hypertrophic type: well circumscribed, elevated white
lesion resembling leukoplakia
-biopsy needed for diagnosis
 Pigmented type: rarely erosive type can be associated with
diffused erythema
-usually on buccal mucosa and vestibule
-reticulated white patches with or without a red erosive
component flanked brown macular foci
Histopathology
 Hyper orthokeratinisation or hyper
parakeratinisation
 Thickening of granular layer
 Acanthosis of spinous layer
 Intercellular oedema in spinous layer
 “Saw-tooth” rete pegs
 Liquefaction necrosis of basal layer
 Civatte ( hyaline or cytoid) bodies
 Juxta epithelial band of inflammatory
cells
Immunofluorescent Studies
 Band of fibrinogen in the
basement membrane zone
 Multiple IgM staining cytoid
bodies in dermal papilla or
peribasalar area
 Highly suggestive of lichen
planus if present in clusters
Differential Diagnosis
 Lichenoid reactions
 Leukoplakia
 Candidiasis
 Pemphigus
 Cicatricial pemphigoid
 Erythema multiforme
 Syphilis
 Recurrent aphthae
 Lupus erythematosus
 Squamous cell carcinoma
Malignant transformation
 Controversy
 Increased risk of oral squamous cell carcinoma
 Frequency of transformation is low, between 0.3% and 3%
 Erosive and atrophic forms commonly undergo
transformation
Treatment
 No cure
 Management of symptoms
 Principal aims: resolution of painful symptoms,
resolution of mucosal lesions, reduction of risk of
cancer & maintenance of good oral hygiene
 Corticosteroids: both systemic & topical
 Topical:
0.05% fluocinonide ( Lidex)
0.05% clobetasol ( Temovate)
as pastes or gels
 Candida overgrowth

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Oral Lichen Planus

  • 2. Oral Lichen Planus Common mucocutaneous disease with varying clinical presentation Premalignant condition Involvement of oral mucosa is frequent along with or preceded by lesions on skin and genital mucous membrane
  • 3. Definition  OLP is a rather common chronic mucocutaneous disease which probably arises due to abnormal immunological reaction and the disease have some tendency to undergo malignant transformation
  • 4. Lichenoid reactions  Exhibits clinical and histological similarity  Distinguished from OLP on the basis of 1. Association with administration of drug, contact with a metal, use of food flavors or systemic diseases 2. Resolution when the cause is eliminated or when disease is treated
  • 5. Epidemiology  Very common- 1% of population  In asians 1.5%(average) 3.7% mixed oral habits 0.3% non users of tobacco  Risk more among who smoke and chew tobacco cutaneous lesion alone 35% mucosal lesion alone 25% both together 40%
  • 6. Etiology  Specific etiology is unknown  Psychological stress  No evident genetic base or no uniform etiologic factors  Abnormal recognition and expression of basal keratinocytes of epithelium as foreign antigens by langerhans cells
  • 7. Pathogenesis CD8 + T cells trigger the apoptosis of oral epithelial cells They recognize an antigen which is similar to an antigen associated with major histocompatability complex class 1 on keratinocytes They release cytokines that attract additional lymphocytes which accumulate in sub basilar connective tissue Liquefaction degeneration of basal keratinocytes
  • 8. Clinical Features  Middle aged or elderly people mean age of onset- 5th decade of life rarely in young adults and children  More in females ( 1.4:1 ) Site- Both skin lesions and mucosal lesions are present
  • 9. Skin Lesions  Purple, pruritic and polygonal papules  May be discreet or gradually coalesce into plaques each covered by fine glistering scale  Bilaterally symmetrical  Increase in size if subjected to any irritation  Usually self limiting unlike the oral lesions lasting only one year or less
  • 10. Skin Lesions  Initially red > purple or violaceous hue > a dirty brownish color  Periods of regression and recurrence  “Koebner’s phenomenon”- skin lesions extend along the areas of injury or irritation  Most often on wrist, forearms, knees, thighs and trunk  Face remains uninvolved
  • 11. Mucosal Lesions  Normally asymptomatic  Bilaterally symmetrical  Sometimes simultaneously have OSF, leukoplakia,etc.  Clinical types 1.reticular 2.atrophic 3.erosive 4.bullous 5. other types
  • 12. Reticular type  Most common and most readily recognized form  Slightly elevated fine whitish lines (Wickham’s striae) in lace like or annular pattern  Lines are wavy and parallel  A tiny elevated dot like structure at the point of intersection of lines  Commonly on buccal mucosa and buccal vestibule
  • 13.
  • 14. Atrophic type  Keratotic changes combined with mucosal erythema  smooth, poorly defined erythematus areas with or without peripheral striae  Usually associated with desquamative gingivitis  Pain and burning sensation
  • 15. Erosive type  Pseudo membrane covered ulcerations with keratosis and erythema  Severe form with extensive degeneration and separation of epithelium from connective tissue  Pain, burning sensation, bleeding, desquamative gingivitis  Commonly on buccal mucosa and vestibule  More dysplasia and malignant transformation
  • 16. Bullous type  Vesciculobullous presentation combined with reticular or erosive pattern  Rare form characterized by large vesicles or bullae (4mm to 2cm)  Lesions usually develop within an erythematus base, rupture immediately leaving painful ulcers  Usually have peripheral radiating striae and seen on posterior part of buccal mucosa
  • 17. Other types  Plaque type: flattened white areas -dorsal surface of tongue -often resemble leukoplakia  Hypertrophic type: well circumscribed, elevated white lesion resembling leukoplakia -biopsy needed for diagnosis  Pigmented type: rarely erosive type can be associated with diffused erythema -usually on buccal mucosa and vestibule -reticulated white patches with or without a red erosive component flanked brown macular foci
  • 18.
  • 19. Histopathology  Hyper orthokeratinisation or hyper parakeratinisation  Thickening of granular layer  Acanthosis of spinous layer  Intercellular oedema in spinous layer  “Saw-tooth” rete pegs  Liquefaction necrosis of basal layer  Civatte ( hyaline or cytoid) bodies  Juxta epithelial band of inflammatory cells
  • 20.
  • 21. Immunofluorescent Studies  Band of fibrinogen in the basement membrane zone  Multiple IgM staining cytoid bodies in dermal papilla or peribasalar area  Highly suggestive of lichen planus if present in clusters
  • 22. Differential Diagnosis  Lichenoid reactions  Leukoplakia  Candidiasis  Pemphigus  Cicatricial pemphigoid  Erythema multiforme  Syphilis  Recurrent aphthae  Lupus erythematosus  Squamous cell carcinoma
  • 23. Malignant transformation  Controversy  Increased risk of oral squamous cell carcinoma  Frequency of transformation is low, between 0.3% and 3%  Erosive and atrophic forms commonly undergo transformation
  • 24.
  • 25. Treatment  No cure  Management of symptoms  Principal aims: resolution of painful symptoms, resolution of mucosal lesions, reduction of risk of cancer & maintenance of good oral hygiene  Corticosteroids: both systemic & topical  Topical: 0.05% fluocinonide ( Lidex) 0.05% clobetasol ( Temovate) as pastes or gels  Candida overgrowth