Anais Brasileiros de Dermatologia (Jun 2017)

Case for diagnosis. Patch granuloma annulare

  • Geraldo Magela Magalhães,
  • Cássio Ferreira Guimarães,
  • Maysa Carla de Paula

DOI
https://doi.org/10.1590/abd1806-4841.20176729
Journal volume & issue
Vol. 92, no. 3
pp. 419 – 420

Abstract

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Abstract A 59-year-old woman reported a 20-day history of slightly scaly erythematous infiltrated patches on her palms and soles with a histopathological result which was consistent with interstitial-pattern granuloma annulare, clinically classified as patch granuloma annulare. This is a rare clinical variant of granuloma annulare, with an unknown incidence and characteristic clinical and histopathological features. The patient evolved with a complete remission of the lesions after biopsy and the use of high-potency topical corticosteroid.

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