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Genetic and Rare Diseases Information Center (GARD)

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Lichen planus pigmentosus


Other Names for this Disease

  • Lichen planus pigmentosa
  • Lichen planus pigmentosus inversus
  • LP pigmentosa
  • LP pigmentosus
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Overview

Lichen planus (LP) pigmentosus is a rare variant of lichen planus and is characterized by the presence of hyperpigmented, dark-brown macules in sun-exposed or skin-fold areas of the body. LP pigmentosus is a rare disease in Europe but it is common in Indian populations and in the Middle East. The disease usually appears in the third and fourth decade of life. The lesions usually do not cause symptoms. The exact cause of LP pigmentosus is unknown but various factors (e.g. viral infections and certain topical agents including mustard oil, amla oil and henna hair dyes) can trigger the disease. Lichen planus pigmentosus seems to follow a chronic and progressive course.[1]
Last updated: 2/29/2012

References

  1. Arnold S. & Cooper S. Lichen planus pigmentosus. Orphanet. May 2011; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=254463. Accessed 8/10/2011.
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In Depth Information

  • Orphanet is a European reference portal for¬†information on rare diseases and orphan drugs.¬† Access to this database is free of charge.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Lichen planus pigmentosus. Click on the link to view a sample search on this topic.
Other Names for this Disease
  • Lichen planus pigmentosa
  • Lichen planus pigmentosus inversus
  • LP pigmentosa
  • LP pigmentosus
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.