Lichen Planus
Leichen ? tree moss ; planus ? flat
Coined by Sir William James Erasmus Wilson in 1869
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Idiopathic, inflammatory disorder affecting skin ,
mucous memb , nails & hair.
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Chronic course with relapses and remissionsAffects 0.5% of the population
Age group affected: 30 ? 60 years
rare in children
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ETIOLOGY :
1. Idiopathic
2. Familial associations: HLAA3, A5, B7, DR1 and
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DRB*0101.
3. Drugs causing LP like eruptions ? gold salts, beta blockers,
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antimalarials, thiazides, furosemide, spironolactone, penicil amine4. Dental amalgams
5. Infections ? HCV
6. Betel leaf, areca nut use in South East Asia - oral LP
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PATHOGENESISThe exact pathomechanisms are unclear
Autoimmunity is clearly suggested to be central in
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pathogenesis in LP1. LP ? specific antigen recognition
2. Cytotoxic Lymphocyte Activation
3. Keratinocyte Apoptosis
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CLINICAL FEATURES
firm, shiny, polygonal, 1?3 mm diameter papules, red to
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violet6 P's --- purple, pruritic, polygonal, plane topped,
papules, plaques
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Pruritus: mild irritation, to continuous severe itching
interfering with sleep
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distribution: isolated/grouped, linear/annularresolved lesions: greyish brown due to
deposition of melanin in the superficial dermis.
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Sites : volar aspect of the wrists, lumbar region,ankles, shins, scalp, palms, soles.
Oral and genital mucosa
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- WICKHAM'S STRIAE :on
BROCQ'S
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close inspection a trace of
PHENOMENON:
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thin white lines seen onSubepidermal
the surface of the lesions
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hemorrhage
following scraping
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of a classical LPlesion
KOEBNER'S PHENOMENON
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Development of
lesions in
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previously normalskin that has been
subjected to trauma
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HISTOPATHOLOGY
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TYPES OF LPMORPHOLOGY
SITE
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SPECIAL
HYPERTROPHIC
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SKINACTINIC
ATROPHIC
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MUCOSAL
LP
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(ORAL, GENITAL)PEMPHIGOIDES
GUTTATE( ERUPTIVE)
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PALMOPLANTAR
LP PIGMENTOSUS
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ANNULARNAIL
LINEAR
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SCALP
VESICULOBULLOUS
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INVERSEFOLLICULAR
ULCERATIVE/EROSIVE
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HYPERTROPHIC LPHypertrophic or warty
lesions
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Lower limbs, especially
around the ankles
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Severely itchyMust be distinguished
from lichen simplex
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chronicus and lichenamyloidosis
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GUTTATE LPLesions are widely
scattered, discrete, size
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(1?2 mm)
Differentiate from
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guttate psoriasisANNULAR LP
very narrow rim of
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activity with a
depressed, slightly
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atrophic centrecharacteristically found
on the penis
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BULLOUS LP
blisters arise only on or
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near the lesions of LP
short duration
HPE - severe liquefaction
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degeneration of the basal
cell layer. Subepidermal
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bulla with typical changesof LP
direct and indirect
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immunofluorescence
negative.
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FOLLICULAR LPFollicular lesions
Scalp
Intensely itchy
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scarring alopeciaACTINIC LP
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Lichen planussubtropicus ?
dark skinned, tropical
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countries
welldefined
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annular/discoid patches,with a deeply
hyperpigmented centre &
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surrounded by a striking
hypopigmented zone
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Sunexposure :central tothe pathogenesis
LICHEN PLANUS PIGMENTOSUS
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India, Middle East
macular
hyperpigmentation:
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slate grey to
brownish black
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face, neck andupper limbs
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LICHEN PLANUS PEMPHIGOIDESacute and generalized
large bullae on both involved
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and uninvolved skin.HPE: subepidermal bulla
without evidence of LP
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Direct IF: linear deposition of
IgG, C3 along basement
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membrane zone inperilesional skin
Immunoelectron
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microscopy: deposition of
IgG,C3 in the base of the
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bulla (unlike BP- roof )LICHEN PLANUS: PALMS, SOLES
lesions are firm, rough
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with a yellowish hue
broadly sheeted or
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punctatediagnosis is very
difficult; syphilis,
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psoriasis, callosities
and warts must be
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excludedMUCOSAL LESIONS
Seen in 30?70% cases; may be isolated
Sites:
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buccal mucosa,
tongue (most often involved)
genitalia- the penile shaft, glans penis, prepuce,
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scrotum, vulvaperianal
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Patterns Of Mucosal Involvement
? Reticulate ? most common
? Atrophic
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? Hypertrophic? Erosive/Ulcerative
? Plaque-like
? Papular
? Bullous
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ORAL LP
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Reticulate
pattern(M/C)
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White streaks, oftenforming a lacework.
inner surface of the
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cheeks, gum
margins, lips.
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Associated oralcandidiasis
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VULVAL LPwelldemarcated
erosions/erythematous areas at
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the vaginal introitus
hyperkeratotic border of lesions;
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Wickham's striae in thesurrounding skin
vaginal inflammation
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pain/burning, scarring/loss ofnormal architecture
involvement of other mucosa
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NAIL INVOLVEMENT
10% cases. Fingernails > toenails
initially 2/3 fingernails, subsequently remaining
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digits.
Exaggerated longitudinal lines, linear depressions
Adhesion between the epidermis of the dorsal
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nail fold and the nail bed: pterygium unguis
complete shedding
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Exaggerated
Pterygium unguis
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longitudinal linesPROGNOSIS / COMPLICATIONS
Lesions resolve with pigmentation that may last for
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many months
Recurrent episodes
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Oral & hypertrophic lesions may be premalignantScarring alopecia
TREATMENT of LP
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:TOPICAL
PHOTOTHERAPY
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SYSTEMIC
TCS
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PUVASTEROIDS
IMMUNOMODULATORS
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RETINOIDS
TRETINOIN
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STEROID SPARING(ORAL LESION)
DRUGS
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LIDOCAINE(ORAL
TETRACYCLINES
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LESION)VIT.D ANALOGUES
DAPSONE
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METRONIDAZOLEGRISEOFULVIN
THALIDOMIDE
BIOLOGICALS
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TREATMENT LADDER:
CUTANEOUS
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First lineLimited: very potent corticosteroids topical (eg.clobetasol
propionate ointment 0.05%);
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Widespread: systemic prednisolone 0.5?1 mg/kg per dayuntil improvement
Second line
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Prednisolone 0.5?1 mg/kg per day until improvementAcitretin 30 mg per day for 8 weeks
PUVA /UVB: two to three times a week ? systemic
retinoids
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TREATMENT LADDER: ORALFirst line
Symptomatic : very potent corticosteroids
Soluble prednisolone tablets, 5 mg in 15 mL water, mouthwash tds or
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betamethasone soluble tablets 0.5 mg
Severe erosive LP: prednisolone 0.5?1 mg/kg per day
Second line
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Papular ,plaquelike white forms no erosions: topical retinoidsResistant to topicals: prednisolone 0.5?1 mg/kg
Third line
Steroid dependent/resistant erosive LP: Azathiprine, MMF, Mtx,
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Cyclosporin ATREATMENT LADDER: NAILS
< four nails
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superpotent corticosteroidsSevere nail involvement :
monthly intralesional injection of triamcinolone acetonide (0.5
?10 mg/mL) in the periungual sites.
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oral prednisolone (0.5?1 mg/kg/day)
LICHEN NITIDUS
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pinpoint to pinheadsized
papules,
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flesh coloured, with a flat,shiny surface. Remain
discrete
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asymptomatic
forearms, penis, abdomen,
chest, buttocks.
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selflimiting, no treatment
intense, circumscribed,
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infiltrate of lymphocytes,histiocytes & few Langhans
cells situated immediately
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below a flattened epidermis.
The rete ridges at the margin
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of the infiltrate are elongatedto encircle it
liquefaction degeneration of
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the basal cell layer.
PITYRIASIS ROSEA
Pityriasis ? scales ; Rosea ? pink ( Gilbert )
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Acute , self-limiting disease , probablyinfective in origin.
Children & young adults with a slight female
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preponderence.
Minimal symptoms - pruritus
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ETIOLOGY:
1. Viral : HHV 7 ; HHV 6 ? reactivation
2. Drugs : Metals ( Ar, Bi, Au)
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LithiumMethopromazine
Metronidazole
Barbiturates
Clonidine
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Captopril etc.CLINICAL FEATURES
HERALD PATCH
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primary plaque/motherpatch.
Sharply defined
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erythematous annularplaque with a peripheral
col arette of scales.
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M/C Site ? thigh,upperarm,trunk or neck
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Within 5-15 daysGeneralised eruption
? discrete oval
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lesions similar to theherald patch but
smaller in size
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Upper chest & back ? Christmas /Inverted Fir
tree pattern.
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Face,scalp ? childrenPalms ? rare, scaly red plaques / diffuse
redness / /small vesicles.
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Oral ? ill defined red patchesAtypical / Morphological Variants:
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papules / vesicles / papulovesicularurticarial
erythema multiforme like
pustular
purpuric
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lichenoidexfoliative dermatitis
Epidermis ? patchy parakeratosis, spongiosis.
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Dermis (upper) ? edema , mononuclear cel infiltrate ( exocytosis intoepidermis forming subcorneal pustules.
TREATMENT :
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Acyclovir ( 800mg 5 times a day x 1 week)
Erythromycin (500mg qid x 2 weeks- adult
40mg/kg div.doses ? child)
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Oral antihistamines
Topical steroids- mid potent
Topical antipruritic lotions
UVB.
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