Case Reports in Dermatology (Jul 2015)

Erythema Dyschromicum Perstans: Identical to Ashy Dermatosis or Not

  • Takafumi Numata,
  • Kazutoshi Harada,
  • Ryoji Tsuboi,
  • Yoshihiko Mitsuhashi

DOI
https://doi.org/10.1159/000437414
Journal volume & issue
Vol. 7, no. 2
pp. 146 – 150

Abstract

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Erythema dyschromicum perstans (EDP) and ashy dermatosis (AD) are pigmentary disorders of unknown etiology. EDP is usually considered to be identical to AD; however, a new clinical classification for EDP was proposed in the recent literature. Herein, we report a typical case of EDP observed in an African-American man. Interestingly, the late skin lesions in this case fit the criteria of AD as well. While there appear to be a few clinical cases that can be diagnosed as both EDP and AD based on the clinical course, the preponderance of the evidence in the published reports of EDP and AD and the clinical findings reported here strongly suggest that they are two distinct entities in terms of the extent of the inflammation, albeit on the same spectrum of pigment disorders.

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