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Papulosquamous diseases
BY
SHATHA ABDELMAWLA ALSULH
ORAL LICHEN
PLANUS
Etiology and Pathogensis:
 Etiology not known
 T-lymphocyte cytotoxicity directed against antigens expressed by the
basal cell layer
 multifactorial: stress
 association with HCV
 Epidemiology
 OLP: 0.5%–2.2%.
Clinical Findings:Oral lichen planus
 To establish a clinical diagnosis of OLP, reticular or papular textures
have to be present
 different clinical manifestations are related to the magnitude of the
subepithelial inflammation
 Symptomes:
 Reticular, popular, plaque like: feeling of roughness
 Bullous, erythematous, ulcerative: smarting sensation
 Reticular: fine white lines
or striae , lace like or
annular, bilaterally in the
buccal mucosa
 Papular: initial phase of the disease , small white dots
Papular oral lichen planus with dense cover of
papules. In the upper left corner, the lesion has started to
form a more reticular structure.
Plaque-like: homogeneous well-demarcated
white plaque in conjunction with striae,
DD: oral leukoplakias, > smokers,
overrepresented in OLP transforming into oral
SCC.
A plaque-like oral lichen planus with a plaque in
the anterior part. In the posterior part, the lesion
has features that are compatible with the
reticular form.
A squamous cell carcinoma developed in a
plaque-like oral lichen planus.
 Bullous: very
unusual , bullous
structures
surrounded by a
reticular network.
Bullous OLP: Single vesicle with surrounding reticular whitish streaks
 Erythematous:
homogeneous red area with
striae in the periphery. If
exclusively affecting
attached gingiva:
desuamative gingivitis that
need histopathology
Desquamative gingivitis secondary to lichen planus.
 Ulcerative:
most disabling,
ulcers
surrounded by
erythema and
peripheral
white striae
Extraoral LP:
 Cutaneous lesions :
 6 P’s: planer (flat topped), pruritic, polygonal, purple, polished (shiny) papules, predilection sites
 may form plaques
 intense scratching
 Koebner phenomenon
 extra-oral mucosal site involved:
 the genital mucosa: 20%, VVG syndrome with erythematous or ulcerative OLP
 Esophageal lichen :dysphagia
 Hair: cicatricial alopecia
 Nail:5–10%
 Longitudinal ridging, splitting and Onycholysis, anonychia,Pterygium
Lichen planus, violaceous, flat-topped papules with minimal scale.
Linear lesions due to Koebner phenomenon in lichen planus
Cicatricial alopecia caused by lichen planus.
Lichen planus, nail involvement with pterygium
 Diagnosis:
 clinical diagnosis: by Papules or reticular components
 A biopsy
 Differential diagnosis:
 Oral GVHD
 Discoid lupus erythematosus (DLE)
 oral leukoplakia
 erythema multiforme
 ulcerative gingivitis
Pathology:
 hyperparakeratosis
 focal hypergranulosis
 Irregular acanthosis & saw-
toothed appearance of the rete
ridges
 interface dermatitis
 hydropic degeneration
 bandlike lymphocytic infiltrate
 melanophages
Management:
 No preventive therapies
 reducing or eliminating symptoms.
 topical drugs :
 Steroids: clobetasol propionate, triamcinolone acetonide.
 calcineurin inhibitors (cyclosporine, tacrolimus and pimecrolimus)
 retinoids
 ultraviolet phototherapy
 systemic steroids for recalcitrant lesions
 OLP is considered to be a premalignant disorder : Albeit the risk is low, a minimum of annual monitoring
has been suggested in conjunction with routine dental examination by the general dental practitioner
Thank you

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6th lecture lichen planus

  • 3. Etiology and Pathogensis:  Etiology not known  T-lymphocyte cytotoxicity directed against antigens expressed by the basal cell layer  multifactorial: stress  association with HCV  Epidemiology  OLP: 0.5%–2.2%.
  • 4. Clinical Findings:Oral lichen planus  To establish a clinical diagnosis of OLP, reticular or papular textures have to be present  different clinical manifestations are related to the magnitude of the subepithelial inflammation  Symptomes:  Reticular, popular, plaque like: feeling of roughness  Bullous, erythematous, ulcerative: smarting sensation
  • 5.  Reticular: fine white lines or striae , lace like or annular, bilaterally in the buccal mucosa
  • 6.  Papular: initial phase of the disease , small white dots Papular oral lichen planus with dense cover of papules. In the upper left corner, the lesion has started to form a more reticular structure.
  • 7. Plaque-like: homogeneous well-demarcated white plaque in conjunction with striae, DD: oral leukoplakias, > smokers, overrepresented in OLP transforming into oral SCC.
  • 8. A plaque-like oral lichen planus with a plaque in the anterior part. In the posterior part, the lesion has features that are compatible with the reticular form. A squamous cell carcinoma developed in a plaque-like oral lichen planus.
  • 9.  Bullous: very unusual , bullous structures surrounded by a reticular network.
  • 10. Bullous OLP: Single vesicle with surrounding reticular whitish streaks
  • 11.  Erythematous: homogeneous red area with striae in the periphery. If exclusively affecting attached gingiva: desuamative gingivitis that need histopathology
  • 13.  Ulcerative: most disabling, ulcers surrounded by erythema and peripheral white striae
  • 14. Extraoral LP:  Cutaneous lesions :  6 P’s: planer (flat topped), pruritic, polygonal, purple, polished (shiny) papules, predilection sites  may form plaques  intense scratching  Koebner phenomenon  extra-oral mucosal site involved:  the genital mucosa: 20%, VVG syndrome with erythematous or ulcerative OLP  Esophageal lichen :dysphagia  Hair: cicatricial alopecia  Nail:5–10%  Longitudinal ridging, splitting and Onycholysis, anonychia,Pterygium
  • 15. Lichen planus, violaceous, flat-topped papules with minimal scale.
  • 16. Linear lesions due to Koebner phenomenon in lichen planus
  • 17. Cicatricial alopecia caused by lichen planus.
  • 18. Lichen planus, nail involvement with pterygium
  • 19.  Diagnosis:  clinical diagnosis: by Papules or reticular components  A biopsy  Differential diagnosis:  Oral GVHD  Discoid lupus erythematosus (DLE)  oral leukoplakia  erythema multiforme  ulcerative gingivitis
  • 20. Pathology:  hyperparakeratosis  focal hypergranulosis  Irregular acanthosis & saw- toothed appearance of the rete ridges  interface dermatitis  hydropic degeneration  bandlike lymphocytic infiltrate  melanophages
  • 21.
  • 22.
  • 23. Management:  No preventive therapies  reducing or eliminating symptoms.  topical drugs :  Steroids: clobetasol propionate, triamcinolone acetonide.  calcineurin inhibitors (cyclosporine, tacrolimus and pimecrolimus)  retinoids  ultraviolet phototherapy  systemic steroids for recalcitrant lesions  OLP is considered to be a premalignant disorder : Albeit the risk is low, a minimum of annual monitoring has been suggested in conjunction with routine dental examination by the general dental practitioner