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LICHEN PLANUS
By-
Dr. Shweta Khushalani
( JR-1, Dept. Skin & V.D.)
Introduction
Idiopathic, chronic, inflammatory disease that
affects the skin, mucous membranes and
appendages.
History
Leichen = tree moss
Planus = flat
Lichen planus = Eramus Wilson,1869
Wickhams striae = Wickham, 1895
Epidemiology
0.1% - 4%
> 45 years of age
Women > men
Child : 1-4% of cases of LP; family history
significant.
Etiopathogenesis
 Unknown, ?AUTOIMMUNE
 ETIOLOGY :
 Idiopathic.
 Drugs.
 Infections & vaccination.
 Associated with autoimmune disorders.
 Contact allergens
 Mechanical trauma
 Genetic association : HLA- A3, BW35, B8, B16,
DR1, DQW1
Drugs
 Heavy metals
 Antimalarials
 Antibiotics
 AKT
 Diuretics
 Antihypertensives
 Anticonvulsant
 NSAIDS
 Oral hypoglycemics
 Antihistaminics
 Lipid lowering agents
 Miscellaneous
Autoimmune disorders
 Ulcerative collitis
 Type 2 DM
 Myasthenia gravis
 Lupus erythematous
 Alopecia aerata
Infections & vaccination
 Hepatitis B & C
 Influenza
 MMR
 DPT
 Antigen specific & nonspecific killing by t-
lymphocytes ( both helper & supressor cells)
 Th17 play imporatnt role, secrete IL-17
 IL-17 upregulate and/or synergize with local
inflammatory mediators and extracellular
matrix injury by MMP (matrix metallo-
protienases)
 Other cytokines-
 TNF-alpha,
 Nuclear factor-Kbeta dependent cytokines
 IFN-gamma
 IL-1alpha, IL-6, IL-8
Clinical features
 Extremely pruritic
 Flat topped
 Polygonal
 Violaceous papules or plaques
 3-15mm in diameter
 Wickhams striae 
 delicate, radiating, white scales
 Focal thickening of granular layer
 Positive Koebners phenomenon
 Sites :
 Flexors surfaces of forearm & wrist, dorsal surface
of hands
 Anterior aspect of lower legs, neck, lower back.
 Heal with hyperpigmentation.
Histology
Lichen Planus Verrucosus
 K/a Hypertrophic LP
 Extremely pruritic
 Hyperkeratotic plaques
on the shin and ankles
 Can transform into
metastatic squamous cell
carcinoma (esp. distal
extremeties)
Atrophic Lichen Planus
 Lower limbs
 Violaceous papules and plaques with depressed
and atropic center
 Usually occurs after resolution of typical LP &
Accentuate by potent topical steroids
Lichen planus
Annular LP
 Glans & trunk
 Typical violaceous papules, in a
ring like fashion
 Central clearing leaving behind
active raised border
 Variant : AALP ( Annular Atrophic
LP)
 Small violaceous papules
 Slowly grow peripherally
 Center:atrophic and hyperpigmented
 Peripherally raised
 Trunk, limbs
Linear LP
 Spontaneous
 Linear along
Lines of
Blaschko
 children > adults
 Rarely, occur at
the site of healed
herpes zoster scar
Bullous LP
 Blisters within the papules
 Liquefactive degeneration
of the basal layer of
epidermis, l/t sub
epidermal blisters, MAX
JOSEPH SPACES
 Extremities, shin (97%) >
upper limbs > thigh
 Chronic course
 Family history present
Lichen planus
LP Pemphigoides
 Blisters on LP lesions + non
affected skin
 Distal limbs
 Histology
 Direct Immunofluorescence
Deposition of IgG & C3 at BMZ
Lichen planus
Actinic LP
 Summer months
 Sun exposed areas, forehead
and face, dorsal surface of
hands and neck
 Blue, brownish plaque,
annular hypopigmented
border with central atrophy
 Young adults & children
 NO PRURITIS
 NO KOEBNERIZATION
LP Pigmentosus
 Slate grey to brownish-
black macules
 sun exposed areas &
flexural folds
 Types
 Diffuse (most common)
 Blotchy
 Reticular
 Perifollicular
Lichen Planopilaris
 a/k/a Follicular LP
 Chronic lymphocytic inflammation around the upper
portion of hair follicle
 Irregular patchy loss of hair, with loss of follicular
ostia.
 Multifocal, patchy > diffuse
 Perifollicular erythema and scaling + on periphery of
the lesion
 Disease activity, periphery>center of the alopecia patch
 Pruritis with dysesthesia
 Site  frontocentral scalp & crown
 50% a/w typical LP lesions over non-follicular
skin, nail, mucous membrane
Perifollicular
lymphocytic
infilterate with
fibroplasia
Erosive LP
 Mucosal surface
 Oral cavity or genitalia
 Erosions on the surface of papular lesions
 Aggressive form of LP
Eruptive LP
 A/k/a acute or exanthematous LP
 Disseminated form
 Trunk, dorsum of feet & wrist
 Self-limiting
 Heal in 3-9months with hyperpigmentation.
Nail LP
 10%
 Finger nails>toe nails
 Adults ( 50-60 years )
 In pediatric age , nail LP>skin LP
 Chronic course
 3 presentations
 Typical Nail LP
 Twenty Nail Dystrophy (trachyonychia)
 Idiopathic Atrophy of Nails
TYPICAL NAIL LP
 diffuse nail ridging
 splitting
 dorsal pterygium
TWENTY NAIL DYSTROPHY
 Excessive longitudnal ridging l/t nail roughness
 Beningn condition
 No nail scarring
 One to several nails affected
IDIOPATHIC ATROPHY OF THE NAIL
 acute & rapid, painless, destruction of the nail
OTHERS
 Yellow nail syndrome like changes
 Nail bed erosions
 Pigmentary changes : longitudnal melanonychia,
longitudnal erythronychia
Lichen planus
TYPICAL NAIL LP
 diffuse nail ridging
 splitting
 dorsal pterygium
TWENTY NAIL DYSTROPHY
 Excessive longitudnal ridging l/t nail roughness
 Beningn condition
 No nail scarring
 One to several nails affected
IDIOPATHIC ATROPHY OF THE NAIL
 acute & rapid, painless, destruction of the nail
OTHERS
 Yellow nail syndrome like changes
 Nail bed erosions
 Pigmentary changes : longitudnal melanonychia,
longitudnal erythronychia
Lichen planus
TYPICAL NAIL LP
 diffuse nail ridging
 splitting
 dorsal pterygium
TWENTY NAIL DYSTROPHY
 Excessive longitudnal ridging l/t nail roughness
 Beningn condition
 No nail scarring
 One to several nails affected
IDIOPATHIC ATROPHY OF THE NAIL
 acute & rapid, painless, destruction of the nail
OTHERS
 Yellow nail syndrome like changes
 Nail bed erosions
 Pigmentary changes : longitudnal melanonychia,
longitudnal erythronychia
Lichen planus
Palmoplantar LP
 Rare
 Highly pruritic,
erythematous, scaly
plaque with/out
plamoplantar
keratoderma
 Internal plantar arch
& hands (NO
FINGERTIPS)
 Young adults (20-40
years age)
Oral LP
 In 70-77% of cutaneous disease
 25% present with oral LP
 Middle age (40-70 years), women
 6 types (ANDREASEN CLASSIFICATION)
 RETICULAR
 PLAQUE-LIKE
 PAPULAR
 EROSIVE
 ATROPHIC
 BULLOUS
 Lateral margins of tongue, gingiva, lips and hard palate
 Chronic course
 STRESS, SPICY & ACIDIC FOOD- flare up
 Association with HCV infection
 Risk of malignant transformation in 0.4-1.5%
RETICULAR LP
 Most common
 Asymptomatic
 Irregular patchy, plaque with white
streaks in a lacy pattern
 posterior buccal mucosa
 Bilateral
EROSIVE ORAL LP
 Large, erythematous, well defines
erosions on buccal mucosa
 with/out pseudomembrane
 Buccal mucosa, Dorsum & lateral
borders of tongue, gingiva
ATROPHIC LP
 Gingiva
 Irritaion following eating & brushing
Lichen planus
Genital LP
 25% cases with skin LP
 Males
 Shaft of penis, glans penis, prepuce, scrotum
 ANNNULAR LP (most common presentation)
 Female
 Vulval and vaginal
 Vulval : on introitus, white lacy, reticular borders extending into vagina
 Dyspareunia
 a/w pruritis and pain
 Loss of normal architecture and scarring on healing
 VVG (VULVO-VAGINAL-GINGIVAL) SYNDROME
 Erosive lesions
 a/w HLA-DQB1*0201 allele
Esophageal LP
 Rare
 Middle age, women, with oral LP
 c/o dysphagia, odynophagia, or both
 Endoscopy
 Strictures & malignant transformation to
Squamous cell carcinoma common
Complications
 Hyperpigmentation
 NAIL LP : dystrophy of nail, anonychia
 LPP SCALP : scarring alopecia
 GENERALISED LP : erythroderma
 ULCERATIVE LP ON FEET : deformity
 HYPERTROPHIC & MUCOSAL LP : malignant
transformation
Treatment
FIRST LINE
 Topical corticosteroids
 First generation antihistaminics (hydroxyzine /
chloprpheniramine)
 Intra-lesional steroids (hypertrophic , nail &
erosive LP)
 Immunomodulator (tacrolimus, pacrolimus)
 Topical minoxidil (LPP)
SECOND LINE
 Systemic corticosteroids (oral or IM)
 Oral prednisolone : 0.5-1mg/kg/day for 4-6 weeks
 Oral mini pulse with betamethsone
 IM inj. Of Triamcinolone :40-80mg, every 6-8
weeks
 Phototherapy
 NB-UVB
 PUVA
 Extracorporeal photopheresis, in recalcitrant & severe
erosive LP
THIRD LINE
 Immunosupressive agents :
 azathioprine,
 Methotrexate ( 10-15mg/week, severe erosive &
generalised LP)
 Cyclophosphamide
 Cyclosporine (severe resistant cutaneous LP & LPP)
 Mycophenolate mofetil
 Hydroxychloroquine : LPP
 Others
 Dapsone
 IFN-alpha
 Isotretenion
 Thalidomide
 sulfasalazine
MUCOSAL LP
 First line : Topical steroids
 Intralesional steroids used in localised ulcerative LP
 Local phototherapy : NB-UVB and PUVA
 excimer 308 nm laser with ECP in recalcitrant oral LP
 Second line :
 Systemic corticosteroids , short term
 Hydroxycholoroquine
THANKYOU

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Lichen planus

  • 1. LICHEN PLANUS By- Dr. Shweta Khushalani ( JR-1, Dept. Skin & V.D.)
  • 2. Introduction Idiopathic, chronic, inflammatory disease that affects the skin, mucous membranes and appendages. History Leichen = tree moss Planus = flat Lichen planus = Eramus Wilson,1869 Wickhams striae = Wickham, 1895
  • 3. Epidemiology 0.1% - 4% > 45 years of age Women > men Child : 1-4% of cases of LP; family history significant.
  • 4. Etiopathogenesis Unknown, ?AUTOIMMUNE ETIOLOGY : Idiopathic. Drugs. Infections & vaccination. Associated with autoimmune disorders. Contact allergens Mechanical trauma Genetic association : HLA- A3, BW35, B8, B16, DR1, DQW1
  • 5. Drugs Heavy metals Antimalarials Antibiotics AKT Diuretics Antihypertensives Anticonvulsant NSAIDS Oral hypoglycemics Antihistaminics Lipid lowering agents Miscellaneous Autoimmune disorders Ulcerative collitis Type 2 DM Myasthenia gravis Lupus erythematous Alopecia aerata Infections & vaccination Hepatitis B & C Influenza MMR DPT
  • 6. Antigen specific & nonspecific killing by t- lymphocytes ( both helper & supressor cells) Th17 play imporatnt role, secrete IL-17 IL-17 upregulate and/or synergize with local inflammatory mediators and extracellular matrix injury by MMP (matrix metallo- protienases) Other cytokines- TNF-alpha, Nuclear factor-Kbeta dependent cytokines IFN-gamma IL-1alpha, IL-6, IL-8
  • 7. Clinical features Extremely pruritic Flat topped Polygonal Violaceous papules or plaques 3-15mm in diameter Wickhams striae delicate, radiating, white scales Focal thickening of granular layer Positive Koebners phenomenon
  • 8. Sites : Flexors surfaces of forearm & wrist, dorsal surface of hands Anterior aspect of lower legs, neck, lower back. Heal with hyperpigmentation.
  • 10. Lichen Planus Verrucosus K/a Hypertrophic LP Extremely pruritic Hyperkeratotic plaques on the shin and ankles Can transform into metastatic squamous cell carcinoma (esp. distal extremeties)
  • 11. Atrophic Lichen Planus Lower limbs Violaceous papules and plaques with depressed and atropic center Usually occurs after resolution of typical LP & Accentuate by potent topical steroids
  • 13. Annular LP Glans & trunk Typical violaceous papules, in a ring like fashion Central clearing leaving behind active raised border Variant : AALP ( Annular Atrophic LP) Small violaceous papules Slowly grow peripherally Center:atrophic and hyperpigmented Peripherally raised Trunk, limbs
  • 14. Linear LP Spontaneous Linear along Lines of Blaschko children > adults Rarely, occur at the site of healed herpes zoster scar
  • 15. Bullous LP Blisters within the papules Liquefactive degeneration of the basal layer of epidermis, l/t sub epidermal blisters, MAX JOSEPH SPACES Extremities, shin (97%) > upper limbs > thigh Chronic course Family history present
  • 17. LP Pemphigoides Blisters on LP lesions + non affected skin Distal limbs Histology Direct Immunofluorescence Deposition of IgG & C3 at BMZ
  • 19. Actinic LP Summer months Sun exposed areas, forehead and face, dorsal surface of hands and neck Blue, brownish plaque, annular hypopigmented border with central atrophy Young adults & children NO PRURITIS NO KOEBNERIZATION
  • 20. LP Pigmentosus Slate grey to brownish- black macules sun exposed areas & flexural folds Types Diffuse (most common) Blotchy Reticular Perifollicular
  • 21. Lichen Planopilaris a/k/a Follicular LP Chronic lymphocytic inflammation around the upper portion of hair follicle Irregular patchy loss of hair, with loss of follicular ostia. Multifocal, patchy > diffuse Perifollicular erythema and scaling + on periphery of the lesion Disease activity, periphery>center of the alopecia patch Pruritis with dysesthesia Site frontocentral scalp & crown
  • 22. 50% a/w typical LP lesions over non-follicular skin, nail, mucous membrane
  • 24. Erosive LP Mucosal surface Oral cavity or genitalia Erosions on the surface of papular lesions Aggressive form of LP Eruptive LP A/k/a acute or exanthematous LP Disseminated form Trunk, dorsum of feet & wrist Self-limiting Heal in 3-9months with hyperpigmentation.
  • 25. Nail LP 10% Finger nails>toe nails Adults ( 50-60 years ) In pediatric age , nail LP>skin LP Chronic course 3 presentations Typical Nail LP Twenty Nail Dystrophy (trachyonychia) Idiopathic Atrophy of Nails
  • 26. TYPICAL NAIL LP diffuse nail ridging splitting dorsal pterygium TWENTY NAIL DYSTROPHY Excessive longitudnal ridging l/t nail roughness Beningn condition No nail scarring One to several nails affected IDIOPATHIC ATROPHY OF THE NAIL acute & rapid, painless, destruction of the nail OTHERS Yellow nail syndrome like changes Nail bed erosions Pigmentary changes : longitudnal melanonychia, longitudnal erythronychia
  • 28. TYPICAL NAIL LP diffuse nail ridging splitting dorsal pterygium TWENTY NAIL DYSTROPHY Excessive longitudnal ridging l/t nail roughness Beningn condition No nail scarring One to several nails affected IDIOPATHIC ATROPHY OF THE NAIL acute & rapid, painless, destruction of the nail OTHERS Yellow nail syndrome like changes Nail bed erosions Pigmentary changes : longitudnal melanonychia, longitudnal erythronychia
  • 30. TYPICAL NAIL LP diffuse nail ridging splitting dorsal pterygium TWENTY NAIL DYSTROPHY Excessive longitudnal ridging l/t nail roughness Beningn condition No nail scarring One to several nails affected IDIOPATHIC ATROPHY OF THE NAIL acute & rapid, painless, destruction of the nail OTHERS Yellow nail syndrome like changes Nail bed erosions Pigmentary changes : longitudnal melanonychia, longitudnal erythronychia
  • 32. Palmoplantar LP Rare Highly pruritic, erythematous, scaly plaque with/out plamoplantar keratoderma Internal plantar arch & hands (NO FINGERTIPS) Young adults (20-40 years age)
  • 33. Oral LP In 70-77% of cutaneous disease 25% present with oral LP Middle age (40-70 years), women 6 types (ANDREASEN CLASSIFICATION) RETICULAR PLAQUE-LIKE PAPULAR EROSIVE ATROPHIC BULLOUS Lateral margins of tongue, gingiva, lips and hard palate Chronic course STRESS, SPICY & ACIDIC FOOD- flare up Association with HCV infection Risk of malignant transformation in 0.4-1.5%
  • 34. RETICULAR LP Most common Asymptomatic Irregular patchy, plaque with white streaks in a lacy pattern posterior buccal mucosa Bilateral EROSIVE ORAL LP Large, erythematous, well defines erosions on buccal mucosa with/out pseudomembrane Buccal mucosa, Dorsum & lateral borders of tongue, gingiva ATROPHIC LP Gingiva Irritaion following eating & brushing
  • 36. Genital LP 25% cases with skin LP Males Shaft of penis, glans penis, prepuce, scrotum ANNNULAR LP (most common presentation)
  • 37. Female Vulval and vaginal Vulval : on introitus, white lacy, reticular borders extending into vagina Dyspareunia a/w pruritis and pain Loss of normal architecture and scarring on healing VVG (VULVO-VAGINAL-GINGIVAL) SYNDROME Erosive lesions a/w HLA-DQB1*0201 allele
  • 38. Esophageal LP Rare Middle age, women, with oral LP c/o dysphagia, odynophagia, or both Endoscopy Strictures & malignant transformation to Squamous cell carcinoma common
  • 39. Complications Hyperpigmentation NAIL LP : dystrophy of nail, anonychia LPP SCALP : scarring alopecia GENERALISED LP : erythroderma ULCERATIVE LP ON FEET : deformity HYPERTROPHIC & MUCOSAL LP : malignant transformation
  • 40. Treatment FIRST LINE Topical corticosteroids First generation antihistaminics (hydroxyzine / chloprpheniramine) Intra-lesional steroids (hypertrophic , nail & erosive LP) Immunomodulator (tacrolimus, pacrolimus) Topical minoxidil (LPP)
  • 41. SECOND LINE Systemic corticosteroids (oral or IM) Oral prednisolone : 0.5-1mg/kg/day for 4-6 weeks Oral mini pulse with betamethsone IM inj. Of Triamcinolone :40-80mg, every 6-8 weeks Phototherapy NB-UVB PUVA Extracorporeal photopheresis, in recalcitrant & severe erosive LP
  • 42. THIRD LINE Immunosupressive agents : azathioprine, Methotrexate ( 10-15mg/week, severe erosive & generalised LP) Cyclophosphamide Cyclosporine (severe resistant cutaneous LP & LPP) Mycophenolate mofetil Hydroxychloroquine : LPP Others Dapsone IFN-alpha Isotretenion Thalidomide sulfasalazine
  • 43. MUCOSAL LP First line : Topical steroids Intralesional steroids used in localised ulcerative LP Local phototherapy : NB-UVB and PUVA excimer 308 nm laser with ECP in recalcitrant oral LP Second line : Systemic corticosteroids , short term Hydroxycholoroquine