TextbookDermatologyLichen Planus

Lichen Planus

A chronic inflammatory dermatosis characterised by pruritic, polygonal, purple, flat-topped papules (the '5 Ps'). Affects skin, mucous membranes, nails, and hair. T-cell mediated attack on basal keratinocytes. Associated with hepatitis C. Usually self-limiting over 1–2 years but oral disease may persist.

Key Facts

5 Ps: Pruritic, Polygonal, Purple, Planar (flat-topped), Papules Wickham's striae: fine white lacy pattern on surface of papules — pathognomonic Oral lichen planus: white reticular pattern on buccal mucosa; erosive form may be premalignant (~1% SCC risk) Koebner phenomenon: lesions develop at sites of skin trauma Hepatitis C association: screen all lichen planus patients for HCV Histology: band-like lymphocytic infiltrate at dermal-epidermal junction, 'saw-tooth' rete ridge pattern, civatte bodies Treatment: potent topical corticosteroids first-line; oral prednisolone for severe disease Self-limiting: cutaneous LP usually resolves within 1–2 years; oral LP may persist for decades

Overview

Key Facts

Lichen planus is a common inflammatory dermatosis that can affect the skin, oral mucosa, genital mucosa, nails, and scalp. It is important because of its association with hepatitis C and the premalignant potential of erosive oral lichen planus.

Epidemiology

  • Prevalence: ~0.5–1% of population
  • Peak age: 30–60 years
  • M:F ~equal for cutaneous; F > M for oral LP
  • Oral LP: 1–2% prevalence in adults

Aetiology

  • T-cell mediated autoimmune: CD8+ cytotoxic T-cells attack basal keratinocytes
  • Hepatitis C: significant association (particularly oral LP); screen all patients
  • Drug-induced lichenoid eruption: beta-blockers, NSAIDs, ACE inhibitors, antimalarials, thiazides, gold
  • Dental amalgam: lichenoid contact reaction
  • Graft-versus-host disease: lichenoid features common

Pathophysiology

  • Cytotoxic T-lymphocytes target basal keratinocyte antigens → apoptosis of basal cells (civatte/colloid bodies)
  • Band-like (lichenoid) lymphocytic infiltrate at dermal-epidermal junction
  • Disruption of basement membrane → pigment incontinence (post-inflammatory hyperpigmentation)
  • 'Saw-tooth' irregular acanthosis of rete ridges on histology

Clinical Presentation

Cutaneous Lichen Planus

  • 5 Ps: Pruritic, Polygonal, Purple/violaceous, Planar (flat-topped), Papules
  • 2–10 mm diameter; shiny surface
  • Wickham's striae: white lacy lines on papule surface
  • Distribution: flexor surfaces (wrists, forearms), shins, lower back
  • Koebner phenomenon: new lesions at sites of trauma
  • Resolves with post-inflammatory hyperpigmentation

Oral Lichen Planus

  • Reticular: white lacy pattern (Wickham's striae) on buccal mucosa — most common; usually asymptomatic
  • Erosive: painful erythematous erosions/ulcers — may affect eating; premalignant (~1% risk of oral SCC)
  • Atrophic: red, glazed areas
  • Bilateral buccal mucosa involvement is characteristic

Other Sites

  • Genital LP: vulval/penile erosions — painful, may cause scarring
  • Nail LP: thinning, longitudinal ridging, pterygium (scarring of nail fold)
  • Scalp (lichen planopilaris): scarring alopecia — irreversible hair loss

Red Flags

  • Erosive oral LP: premalignant — requires long-term monitoring
  • Scarring alopecia (lichen planopilaris) — irreversible
  • Oesophageal LP: dysphagia — rare
  • Drug-induced: review medication list

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
PsoriasisSilvery scale, extensor surfaces, nail pittingClinical, biopsy
Drug eruption (lichenoid)Temporal relationship with drug, more widespreadDrug history, biopsy
EczemaPoorly defined, flexural, exudativeClinical
Secondary syphilisWidespread rash, palms/soles, lymphadenopathySyphilis serology
Oral leukoplakiaWhite patch, cannot be rubbed off, no Wickham's patternBiopsy to exclude dysplasia
Graft-versus-host diseasePost-transplant, lichenoid featuresClinical context, biopsy

Diagnosis / Investigation

Bedside

  • Clinical examination: characteristic morphology, Wickham's striae (use dermoscopy), Koebner phenomenon
  • Oral examination: reticular/erosive changes on buccal mucosa
  • Genital, nail, and scalp examination

Bloods

  • Hepatitis C serology: screen ALL lichen planus patients
  • LFTs: hepatitis C association
  • FBC, U&Es: baseline if considering systemic treatment

Biopsy

  • Punch biopsy: band-like lymphocytic infiltrate at DEJ, 'saw-tooth' rete ridges, civatte bodies (apoptotic keratinocytes), hypergranulosis
  • DIF: rarely needed; may show fibrinogen deposition at BMZ (shaggy fibrin)

Special Tests

  • Dermoscopy: Wickham's striae appear as white crossing lines
  • Oral biopsy: for erosive oral LP — exclude dysplasia/SCC

Management

Non-Pharmacological

  • Patient education: usually self-limiting (1–2 years for cutaneous LP)
  • Avoid triggers: review medications for lichenoid drug eruptions; dental amalgam consideration
  • Oral LP monitoring: 6–12 monthly review for erosive disease (malignant potential)

Pharmacological

Cutaneous LP:

  • Potent topical corticosteroids: clobetasol propionate 0.05% or betamethasone valerate 0.1% — first-line
  • Topical tacrolimus 0.1% ointment: steroid-sparing alternative
  • Oral prednisolone 0.5–1 mg/kg: short course for severe/widespread disease
  • Acitretin 25–50 mg OD: for widespread, refractory cutaneous LP
  • Phototherapy (narrowband UVB): for widespread disease

Oral LP:

  • Topical corticosteroid mouthwash/paste: betamethasone 0.5 mg dissolved in 10 mL water as mouthwash; or clobetasol in adhesive paste
  • Topical tacrolimus 0.1%: for erosive oral LP
  • Oral prednisolone: short course for severe erosive flares

Lichen planopilaris:

  • Potent topical steroids to scalp
  • Hydroxychloroquine 200 mg BD: first-line systemic
  • Aim to halt progression — scarring alopecia is irreversible

Referral Criteria

  • Dermatology: severe/widespread disease, erosive oral LP, lichen planopilaris
  • Oral medicine/maxillofacial: erosive oral LP — long-term monitoring
  • Hepatology: if hepatitis C positive

Prognosis

  • Cutaneous LP: usually self-limiting within 1–2 years; ~20% may recur
  • Oral LP: may persist for decades; erosive form requires long-term monitoring
  • Erosive oral LP: ~1% risk of progression to oral SCC over 5–10 years
  • Lichen planopilaris: scarring alopecia is irreversible — early treatment to halt progression
  • Nail LP: may cause permanent nail dystrophy
  • Post-inflammatory hyperpigmentation: common, especially in darker skin types; may persist for months–years

Other Relevant Information

Lichen Planus Variants

VariantFeatures
Cutaneous5 Ps, Wickham's striae, flexor surfaces
Oral (reticular)White lacy pattern, buccal mucosa, asymptomatic
Oral (erosive)Painful erosions, premalignant (~1% SCC)
Lichen planopilarisScarring alopecia, follicular keratosis
Nail LPThinning, ridging, pterygium
Hypertrophic LPThick, verrucous plaques on shins
Genital LPErosive, painful, may cause scarring

Lichenoid Drug Reactions — Common Culprits

Drug ClassExamples
Beta-blockersAtenolol, propranolol
ACE inhibitorsEnalapril, captopril
AntimalarialsHydroxychloroquine
Thiazide diureticsBendroflumethiazide
NSAIDsIbuprofen
GoldSodium aurothiomalate