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Lichen Planus
Dr. Prajwal Pandey
Department of Dermatology
Introduction
• Lichen
• Lichenoid
– Clinical
– Histological
• “bandlike” infiltrate of mononuclear inflammatory cells
(predominantly lymphocytes) immediately subjacent to the
dermal–epidermal junction
• Lichen Planus
• 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
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
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
Sites of
predilection
Characteristic oral/mucosal finding
• Involved in 50% of LP, sole manifestation in 10%
• Wickham’s stria, in absence of papular component
– White, retiulated, netlike pattern
– Buccal mucosa, tongue, other mucosal surface
• Asymptomatic to erosive form: erosive gingivitis
• Some cases associated with dental amalgams
(mercury)
– Mercury-associated lichenoid stomatitis
• 25% involvement in genital mucosa
Pathogenesis
• Cause unknown
• Hypotheses
– Hypersensitivity reaction
– Viral infection (hepatitis C)
– Autoimmune mechanisms
• Lichenoid eruptions
– Drugs
– Graft vs host disease (bone marrow transplant)
• Dental amalgum
• Idiopathic (most cases)
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
Variants
• Clinical and histological variants
– Annular
– Hypertrophic
– Ulcerative
– Vesicobullous/ LP pemphigoides
– Actinic
– Lichen planopilaris (follicular)
• Scarring alopecia in scalp involvement
• Frontal fibrosing alopecia
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
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
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
Treatment
• Pruritus in mild cases
– Topical corticosteroids
– Oral antihistamines
• Severe disease
– Optimal treatment difficult to determine
– Systemic corticosteroids most commonly
– Topical calcineurin inhibitors (tacrolimus, pimecrolimus)
– Psoralen UVA, narrow-band UVB
– Oral retinoids (isotretinoin and acitretin)
– Others: Dapsone, griseofulvin, methotrexate, cyclosporine,
sulfasalazine, thalidomide
Treatment
Guidelines
Differentials
• Lichenoid drug eruption
– Atypical distribution
– Lack of mucosal involvement
– Histopathology
• significant parakeratosis
• eosinophils within the inflammation
• Lichenoid contact dermatitis
– Chemicals involved in photodeveloping
Common drugs implicated in Lichenoid
Drug Eruption
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
Lichen Planus: A Guide to Clinical Features, Pathogenesis, Treatment and Differentials

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Lichen Planus: A Guide to Clinical Features, Pathogenesis, Treatment and Differentials

  • 1. Lichen Planus Dr. Prajwal Pandey Department of Dermatology
  • 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
  • 8. Characteristic oral/mucosal finding • Involved in 50% of LP, sole manifestation in 10% • Wickham’s stria, in absence of papular component – White, retiulated, netlike pattern – Buccal mucosa, tongue, other mucosal surface • Asymptomatic to erosive form: erosive gingivitis • Some cases associated with dental amalgams (mercury) – Mercury-associated lichenoid stomatitis • 25% involvement in genital mucosa
  • 9. Pathogenesis • Cause unknown • Hypotheses – Hypersensitivity reaction – Viral infection (hepatitis C) – Autoimmune mechanisms • Lichenoid eruptions – Drugs – Graft vs host disease (bone marrow transplant) • Dental amalgum • Idiopathic (most cases)
  • 10.
  • 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
  • 12. Variants • Clinical and histological variants – Annular – Hypertrophic – Ulcerative – Vesicobullous/ LP pemphigoides – Actinic – Lichen planopilaris (follicular) • Scarring alopecia in scalp involvement • Frontal fibrosing alopecia
  • 13.
  • 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
  • 17.
  • 18. Treatment • Pruritus in mild cases – Topical corticosteroids – Oral antihistamines • Severe disease – Optimal treatment difficult to determine – Systemic corticosteroids most commonly – Topical calcineurin inhibitors (tacrolimus, pimecrolimus) – Psoralen UVA, narrow-band UVB – Oral retinoids (isotretinoin and acitretin) – Others: Dapsone, griseofulvin, methotrexate, cyclosporine, sulfasalazine, thalidomide
  • 20. Differentials • Lichenoid drug eruption – Atypical distribution – Lack of mucosal involvement – Histopathology • significant parakeratosis • eosinophils within the inflammation • Lichenoid contact dermatitis – Chemicals involved in photodeveloping
  • 21. Common drugs implicated in Lichenoid Drug Eruption
  • 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