Introduction:
Is chronic eruption consisting of multiple tiny discrete skin coloured papuples that are arranged in clusters.Progression from lichen nitidus to lichen planus has been reported. Few authours believe it may be a clincal manifestation of crohn's disease, however it is generally accepted that lichen nitidus is not associated with any systemic disease or abnormal laboratory findings.
Exhibits Koebner phenomenon.
Clinical Features:
Symptoms
Pruritis can occur but it is an uncommon feature.
Signs
Numerous, tiny, discrete,shiny skin colured uniform, pinhead-sized papules that occasionally exhibit central depression.
Lesions can coalesce to form plaques that can have psoriasiform appearance esp on elbows and knees
Papules can be hypopigmented in dark skin individuals,however occaionslly can be hyperpimented.
Location
Flexor aspect of upper extremities,genetalis,
chest,abdomen and dorsum of hands.
oral lesions are rare.
Nail involvement in about 10 % of patients.(same findings as LP)
Pathology
Infiltrate of lymphocytes, epitheloid cells and occaionally langhans giant cells is typically clutched by the surrounding hyperplastic rete ridges in a "ball and claw" pattern.
Lichenoid infiltrate closely apposes the epidermis.
Treatment
Treatment is mainly symtomatic.
First Line
Topical steriods
Anti histamines
Topical Calcineurim inhibitors
Second Line
Same as LP
Prognosis
Two thirds of patients resolve within a year.
I have this condition for about 8 years,and now I'm under treatment,how long will it take to resolve
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Lichen planus pigmentosus specialist