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
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Psoriasis | Silvery scale, extensor surfaces, nail pitting | Clinical, biopsy |
| Drug eruption (lichenoid) | Temporal relationship with drug, more widespread | Drug history, biopsy |
| Eczema | Poorly defined, flexural, exudative | Clinical |
| Secondary syphilis | Widespread rash, palms/soles, lymphadenopathy | Syphilis serology |
| Oral leukoplakia | White patch, cannot be rubbed off, no Wickham's pattern | Biopsy to exclude dysplasia |
| Graft-versus-host disease | Post-transplant, lichenoid features | Clinical 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
| Variant | Features |
|---|---|
| Cutaneous | 5 Ps, Wickham's striae, flexor surfaces |
| Oral (reticular) | White lacy pattern, buccal mucosa, asymptomatic |
| Oral (erosive) | Painful erosions, premalignant (~1% SCC) |
| Lichen planopilaris | Scarring alopecia, follicular keratosis |
| Nail LP | Thinning, ridging, pterygium |
| Hypertrophic LP | Thick, verrucous plaques on shins |
| Genital LP | Erosive, painful, may cause scarring |
Lichenoid Drug Reactions — Common Culprits
| Drug Class | Examples |
|---|---|
| Beta-blockers | Atenolol, propranolol |
| ACE inhibitors | Enalapril, captopril |
| Antimalarials | Hydroxychloroquine |
| Thiazide diuretics | Bendroflumethiazide |
| NSAIDs | Ibuprofen |
| Gold | Sodium aurothiomalate |