Anais Brasileiros de Dermatologia (Dec 2013)

Lichen planus pigmentosus inversus

  • Hugo Rocha Barros,
  • José Roberto Paes de Almeida,
  • Sandra Lopes Mattos e Dinato,
  • Angelo Sementilli,
  • Ney Romiti

DOI
https://doi.org/10.1590/abd1806-4841.20132599
Journal volume & issue
Vol. 88, no. 6 suppl 1
pp. 146 – 149

Abstract

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Twenty-five year old male patient presenting with asymptomatic brown spots, on cervical, axillary, inguinal and popliteal regions, for the last nine months. Pathological examination showed hydropic degeneration of the basal layer, pigmentary incontinence and moderate inflammatory lymphocytic infiltrate in the dermis. Lichen planus pigmentosus inversus is a rare subtype of lichen planus characterized by hyperchromic, asymptomatic or mildly pruritic macules, measuring from millimeters to centimeters in diameter, with defined borders, affecting intertriginous areas, most commonly in the axillae and groin of Caucasian patients. It presents unique lichenoid histology. We report a case with typical clinical features, histology and evolution.

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