2. Introduction
• Lichen
• Lichenoid
– Clinical
– Histological
• “bandlike” infiltrate of mononuclear inflammatory cells
(predominantly lymphocytes) immediately subjacent to the
dermal–epidermal junction
• Lichen Planus
3. • Relatively common (1% of all dermatology
visits)
• Most often affects middle-aged adults, female
slightly more than male
• Both skin and mucosa are involved
– Examination of all sites essential if suspected
4. Primary lesions of LP
• ‘P’s in LP
– Plentiful
– Pruritic
– Polished
– Purple
– Polygonal
– Plane
– Papules/plaques
• Wickham’s stria
– Only diagnostic clue in
mucosal involvement
– Can be enhanced by drop
of mineral oil
• Isomorphism
5.
6. Primary Symptom
• Onset: acute or insidious
• Pruritus often intense
• Special quality of pruritus
– Induces rubbing rather than scratching for relief
– May account for polished appearance
• Koebnerization
– New lesions at the site of excoriation
11. Less common presentations
• Nail changes
– 10 – 15 %
– Longitudinal ridging, irregular pitting, nail plate splitting, nail
loss
– Pup tent sign: tenting of nail plate
– Pterygium formation
– 20 nail dystrophy
• Desquamative vaginitis
• Annular LP in glans
– characteristic
14. Associated systemic diseases
• Viral hepatitis (HCV)
– Association in East/Southeast Asia, South America, Middle East
and Europe
– Ask Hx of: IV drug use, high risk sexual behavior, blood
transfusion
• Chronic active hepatitis
• Primary biliary cirrhosis
• Diabetes mellitus
• Internal malignancy
• Autoimmune or connective tissue disease
15. Prognosis
• Duration related to the site of involvement
• Isolated mucosal lesions
– More chronic (lasting decades)
– Increased risk of SCC
• Isolated cutaneous lesions
– Typical spontaneous resolution, 1-2 years
• Both mucosal and cutaneous involvement
– Intermediate prognosis
• Persistent and recalcitrant
– Ulcerative, Palmoplantar and actinic variants
16. Histopathology
• Hyperkeratotic stratum corneum, essentially no
parakeratosis
• Granular layer focally accentuated: wedge shaped
hypergranulosis
• Malphighian layer irregularly thickened: sawtooth
acanthosis, civatte bodies in superficial dermis
• Interface reaction: lost or flattened basal layer
• Bandlike lymphocytic infiltrate with vacuolated and
obscured DEJ: lichenoid infiltration
22. LP and other rare associations
• LP-SLE overlap syndrome
– SLE diagnosed in patients with LP
– Papulosquamous lesions of SLE in acral area may resemble
LP
• Lichen planus pemphigoides
– Overlapping features of LP and bullous pemphigoid
– Bullous lesions arising on LP-like papules and normal skin
• Lichenoid eruptions in GVHD
– More generalized than classic LP
– Clinically and histologically indistinguishable