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By
M.D.
Lichen planus has been described
as an
 autoimmune disease
 a papulosquamous disorder
 a mucocutaneous disease
 an inflammatory disease
EPIDEMIOLOGY
 Risks :
– Drugs: Exposure to medicines, dyes, and
other chemicals such as gold, chloroquine,
quinacrine, quinide, phenothiazines, and
diuretics)
– Diseases such as HCV, GVHD
 Race: No racial predispositions
 Sex: M:F=2:3
 Age: Any ag, more in adults, 30-60 y
Epidemiology
Variants
6-LP of the Nails1-Classic
7-LP of the MM2-Hypertrophic
8-Erytheodermic LP3-Annular atrophic
9-Vsiculo-bullous4-Actinic
10-LP-pemphigoides5-Planopilaris
Oral lichen
Oral lesions
White fixed plaques
 Squamous cell carcinoma in
oral ulcerative lesions.
 Cicatricial alopecia in scalp LP.
 Post-inflammatory hyperpigm.
Complications of LP
SystemicTopical
Steroids, MTX,
Azathioprine,Hydroxych
loroquine
Topical steroids
Metronidazole,
Griseofulvin
Intralsional steroids
Acitretin, Thalidomide,
Isotretinion
Tretinoin
CelceptCyclosporine,
Dapsone, Biologics
Tacrolimus, Calcipotriol
Treatment
Treatment of LPP
 Avoid triggering factors
 Photo protection: every 2-4 hours
 High potency steroids, not in the inversus
 Tacrolimus ointment
 Depigmenting agents
 Chemical peels (G or TCA 30%)
 Q-Switched nd YAG
Treatment of LPP
 Systemic steroids: pulse therapy
 or deflazacort 45 mg/day
 Dapsone 100 mg/day
 Isotretinion
Course and Outcome
 No curative drug
 LP can flare up years after being cured.
 The condition often clears up within 18
months but may come and go for years.
Lichen planus diagnostic and therapeutic challenges

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Lichen planus diagnostic and therapeutic challenges

  • 1.
  • 3.
  • 4. Lichen planus has been described as an  autoimmune disease  a papulosquamous disorder  a mucocutaneous disease  an inflammatory disease
  • 5. EPIDEMIOLOGY  Risks : – Drugs: Exposure to medicines, dyes, and other chemicals such as gold, chloroquine, quinacrine, quinide, phenothiazines, and diuretics) – Diseases such as HCV, GVHD  Race: No racial predispositions  Sex: M:F=2:3  Age: Any ag, more in adults, 30-60 y Epidemiology
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  • 10. Variants 6-LP of the Nails1-Classic 7-LP of the MM2-Hypertrophic 8-Erytheodermic LP3-Annular atrophic 9-Vsiculo-bullous4-Actinic 10-LP-pemphigoides5-Planopilaris
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  • 202.  Squamous cell carcinoma in oral ulcerative lesions.  Cicatricial alopecia in scalp LP.  Post-inflammatory hyperpigm. Complications of LP
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  • 207. SystemicTopical Steroids, MTX, Azathioprine,Hydroxych loroquine Topical steroids Metronidazole, Griseofulvin Intralsional steroids Acitretin, Thalidomide, Isotretinion Tretinoin CelceptCyclosporine, Dapsone, Biologics Tacrolimus, Calcipotriol Treatment
  • 208.
  • 209. Treatment of LPP  Avoid triggering factors  Photo protection: every 2-4 hours  High potency steroids, not in the inversus  Tacrolimus ointment  Depigmenting agents  Chemical peels (G or TCA 30%)  Q-Switched nd YAG
  • 210. Treatment of LPP  Systemic steroids: pulse therapy  or deflazacort 45 mg/day  Dapsone 100 mg/day  Isotretinion
  • 211.
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  • 213. Course and Outcome  No curative drug  LP can flare up years after being cured.  The condition often clears up within 18 months but may come and go for years.

Editor's Notes

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