Lichen Planus

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oPatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

Lichen planus is a pruritic, papular eruption characterised by its violaceous colour and polygonal shape, sometimes with a fine scale. It is most often found on the flexor surfaces of the upper extremities, genitalia and on the mucous membranes. The cause of lichen planus is unknown but it is most likely a T-cell-mediated immunological disease. The antigen involved remains unidentified.[1] An association with hepatitis C has been noted.[2] 

  • It can occur at any age but is uncommon in the very young or elderly. One UK study found it occurred chiefly in persons aged over 45 years, with an annual incidence (all ages) in 2003 of 27 per 100,000.[3]
  • Most studies report no gender predilection but a few have found a slight preponderance in females.
  • Can be precipitated by trauma (Köbner's phenomenon).
  • Immunologically mediated (perhaps triggered by a virus) and can occur in families.
  • Associated with primary biliary cirrhosis.[4] 
  • Onset is usually acute, affecting the flexor surfaces of the wrists, forearms and legs.
  • The typical lesion is an intensely itchy 2-5 mm red or violet shiny flat-topped papule with white streaks ('Wickham's striae').
    LICHEN PLANUS -ON WRIST
  • Blisters occasionally occur.
  • As the papules clear they may be replaced by brown discolouration (especially in the dark-skinned). Lesions may occur on any part of the body surface but most commonly on the front of the wrists, flexor aspects of the forearms, genitals, lumbar region and the ankles and shins (where lesions are most commonly hypertrophic, frequently very itchy and may ulcerate).
  • On the palms and soles the papules are firm and yellow.
  • Mucous membranes are commonly affected:
    • Classically, white slightly raised lesions with a trabecular, lacy appearance on the inside of the cheeks.
      LICHEN PLANUS
    • The mucous membrane lesions are often asymptomatic but can be very painful and difficult to treat. Oral lichen planus may cause sensitivity to heat. There is also an association with mercury fillings.[5] 
    • Lesions may also be found on the genitalia, anus, larynx and, very rarely, on the tympanic membrane or oesophagus (where it can present as dysphagia and cause benign strictures).
  • Nails are involved in up to 10% of patients: longitudinal lines and linear depressions of the nail plate, severe dystrophy and complete destruction of the nail bed may occur.
  • The scalp is usually spared but lichen planus affecting the scalp may cause permanent scarring alopecia.

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Variations of lichen planus

As well as the classical form, the following can occur:

  • Hypertrophic lichen planus - this causes very itchy lesions, usually found on the extensor surfaces of the extremities, especially the ankles. They can last for a long time and leave residual scarring and pigmentation.
  • Atrophic lichen planus - a few lesions are present which are often resolving annular or hypertrophic lesions.
  • Erosive/ulcerative lichen planus - found on mucosal surfaces and develop from sites where lichen planus previously developed.
  • Follicular lichen planus - this is also known as lichen planopilaris. Keratotic papules are present that may merge into plaques. The condition is more common in women than in men and often involves mucous membranes and nails. A scarring alopecia sometimes develops.
  • Annular lichen planus - purely annular lesions are rare. Papules with an atrophic centre may develop on the male genitalia or the buccal mucosa.
  • Vesicular and bullous lichen planus - usually these develop from existing areas of lichen planus. The lower limbs and the mouth are the most common areas. Rarely, a combination of lichen planus and bullous pemphigoid can develop, called lichen planus pemphigoides.
  • Actinic lichen planus - this is seen in subtropical regions such as Africa, the Middle East and India. The typical appearance is of nummular patches with a hyperpigmented centre surrounded by a hypopigmented area. The condition is mildly itchy and often spares the nails, scalp, mucous membranes and covered areas.
  • Lichen planus pigmentosus - more commonly affects darker skin - eg, people from Latin America or Asia are commonly affected. It resembles another condition called erythema dyschromicum perstans (ashy dermatosis) and some authorities maintain that it is indeed the same condition. It is relatively rare.

Lichen planus can usually be diagnosed clinically and histology is not often required. Skin biopsy is characteristic:

  • There is a 'saw-tooth' pattern of epidermal hyperplasia and vacuolar alteration of the basal layer of the epidermis along with an intense upper dermal band-like lymphohistiocytic infiltrate (mainly T cells).
  • This initially develops around blood vessels at the dermal/epidermal junction and disrupts the basal epidermal layer.
  • There is a reduced number of melanocytes in this region and focal areas with a thicker granular layer and infiltrate (the 'Wickham's striae').
  • Direct immunofluorescence shows globular deposits of IgM (occasionally IgG and IgA).
  • Treatment is not always needed. Skin lichen planus may resolve spontaneously within a year, although mucous membrane lichen planus may be more persistent and resistant to treatment.
  • If drugs are suspected as the cause, they should be stopped.
  • Symptomatic treatment for itching - eg, moderately potent topical steroids (intralesional steroid injections may be beneficial for patients with severe and persistent itch) and sedating antihistamines.
  • Occlusional treatment using potent or super-potent steroids is occasionally used for persistent lesions, particularly on the shins. Occlusion is best obtained using cling film or Icthopaste® bandage.
  • Extensive cases may merit systemic steroids (20 mg of oral prednisolone for fourteen days) to lessen the itch and often clear up the lichen planus completely (although it may recur).
  • Topical steroids are considered to be the first-line treatment for oral lichen planus although there are no randomised controlled trials comparing them with placebo. There is weak evidence to support the use of ciclosporin and aloe vera.[7] 
  • Psoralen combined with ultraviolet A (PUVA) radiation treatment may reduce pruritus and help to clear the lichen planus.[8] 
  • Topical and systemic retinoids (eg, isotretinoin) have been used for oral lichen planus.[9] 
  • Levamisole has been used with some success in oral lichen planus.[10] 
  • Topical immunomodulators (eg, imiquimod) may be useful as second-line treatment in severe oral lichen planus.[11]
  • Low-level laser therapy has been used successfully for ulcerative/erosive oral lichen planus.[12] 
  • Oral lichen planus carries a very small risk of malignant change, particularly in men. Human papillomavirus may have a role in this change.[1] 
  • Squamous cell carcinoma has been reported in oral lichen planus. Reported incidence varies widely in the literature and ranges from 0-12.5%.[13] 
  • Rarely, squamous cell carcinoma may develop in association with vulval lesions in women.[14] 
  • Hypertrophic lesions may leave residual hyperpigmentation.
  • Spontaneous resolution of cutaneous lesions usually occurs over a period of 6 to 12 months but hypertrophic lesions can last for years.
  • Oral lesions usually have a chronic and progressive course and may never completely resolve.
  • The degree of pruritus tends to decrease with time.

Further reading & references

  1. Gorouhi F, Davari P, Fazel N; Cutaneous and mucosal lichen planus: a comprehensive review of clinical subtypes, risk factors, diagnosis, and prognosis. ScientificWorldJournal. 2014 Jan 30;2014:742826. doi: 10.1155/2014/742826. eCollection 2014.
  2. Halawani M; Hepatitis C virus genotypes among patients with lichen planus in the Kingdom of Saudi Arabia. Int J Dermatol. 2014 Feb;53(2):171-7. doi: 10.1111/j.1365-4632.2012.05685.x. Epub 2013 May 15.
  3. Pannell RS, Fleming DM, Cross KW; The incidence of molluscum contagiosum, scabies and lichen planus. Epidemiol Infect. 2005 Dec;133(6):985-91.
  4. Nagao Y, Sata M; Disappearance of Oral Lichen Planus After Liver Transplantation for Primary Biliary Cirrhosis and Immunosuppressive Therapy in a 63-year-Old Japanese Woman. Hepat Mon. 2014 Mar 11;14(3):e16310. doi: 10.5812/hepatmon.16310. eCollection 2014 Mar.
  5. Laeijendecker R, Dekker SK, Burger PM, et al; Oral lichen planus and allergy to dental amalgam restorations. Arch Dermatol. 2004 Dec;140(12):1434-8.
  6. Lichen Planus; Primary Care Dermatology Society
  7. Lodi G, Carrozzo M, Furness S, et al; Interventions for treating oral lichen planus: a systematic review. Br J Dermatol. 2012 May;166(5):938-47. doi: 10.1111/j.1365-2133.2012.10821.x. Epub 2012 Mar 27.
  8. Wackernagel A, Legat FJ, Hofer A, et al; Psoralen plus UVA vs. UVB-311 nm for the treatment of lichen planus. Photodermatol Photoimmunol Photomed. 2007 Feb;23(1):15-9.
  9. Fornaini C; LLLT in the Symptomatic Treatment of Oral Lichen Planus. Laser Ther. 2012 Mar 28;21(1):51-3. doi: 10.5978/islsm.12-CR-03.
  10. Won TH, Park SY, Kim BS, et al; Levamisole monotherapy for oral lichen planus. Ann Dermatol. 2009 Aug;21(3):250-4. doi: 10.5021/ad.2009.21.3.250. Epub 2009 Aug 31.
  11. Elad S, Epstein JB, von Bultzingslowen I, et al; Topical immunomodulators for management of oral mucosal conditions, a systematic Expert Opin Emerg Drugs. 2011 Mar;16(1):183-202. Epub 2011 Jan 19.
  12. Mahdavi O, Boostani N, Jajarm H, et al; Use of low level laser therapy for oral lichen planus: report of two cases. J Dent (Shiraz). 2013 Dec;14(4):201-4.
  13. Budimir V, Richter I, Andabak-Rogulj A, et al; Oral lichen planus - retrospective study of 563 Croatian patients. Med Oral Patol Oral Cir Bucal. 2014 May 1;19(3):e255-60.
  14. Regauer S, Reich O, Eberz B; Vulvar cancers in women with vulvar lichen planus: A clinicopathological study. J Am Acad Dermatol. 2014 Jul 3. pii: S0190-9622(14)01546-1. doi: 10.1016/j.jaad.2014.05.057.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Colin Tidy
Current Version:
Peer Reviewer:
Prof Cathy Jackson
Document ID:
2385 (v24)
Last Checked:
12/08/2014
Next Review:
11/08/2019