Lichen planus

Lichen planus is a chronic inflammatory disease of unknown origin, which most commonly affects individuals between 30–60 years of age and is characterized by different types of lesions involving the skin and mucosa.

Epidemiology


Etiology


Pathophysiology


Clinical features


Cutaneous lichen planus

Oral white lesions#Oral lichen planus

Diagnostics


Pathology

Differential Diagnostics


Psoriasis vs Lichen planus

  • Immune Mechanism:
    • Lichen Planus primarily involves CD8+ T cells targeting basal keratinocytes, creating a band-like lymphocytic infiltrate at the dermo-epidermal junction and interface dermatitis
    • Psoriasis is driven by Th17/Th1 cells and involves complex cytokine cascades (IL-17, IL-22, TNF-α), affecting the entire epidermis and leading to neutrophil recruitment
  • Keratinocyte Response:
    • Lichen Planus shows normal to slow keratinocyte turnover, allowing time for proper differentiation, resulting in hypergranulosis (increased keratohyalin granules)
      • Because of immune stress?
    • Psoriasis exhibits extremely rapid keratinocyte turnover (3-5 days vs normal 28-30 days), preventing proper differentiation, leading to loss of granular layer and parakeratosis

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Feature Psoriasis Lichen Planus
Appearance Red plaques with silvery scales Flat-topped, purple papules with white lines
Common Sites Scalp, elbows, knees, lower back, nails Wrists, ankles, oral/genital mucosa
Itchiness Often mild or absent Frequently intense
Nail Involvement Common (pitting, onycholysis) Possible (thinning, ridging)
Mucosal Involvement Rare Common, especially mouth
Auspitz Sign Present Absent
Histopathology Acanthosis, parakeratosis, Munro abscesses Saw-tooth lymphocytes, Civatte bodies
Associated Conditions Psoriatic arthritis, metabolic syndrome Hepatitis C, other autoimmune diseases

Treatment