[Extensive Dowling-Degos disease following long term PUVA therapy]

Ann Dermatol Venereol. 2012 Jan;139(1):54-7. doi: 10.1016/j.annder.2011.10.403. Epub 2011 Dec 6.
[Article in French]

Abstract

Background: Dowling-Degos disease is a rare and benign inherited dermatosis.

Patients and methods: A 53-year-old woman presented with generalized histologically confirmed Dowling-Degos disease revealed 8 years after psoralen photochemotherapy (PUVA) for psoriasis. This presentation was special in terms of its considerable spread as well as the absence of comedone-like and punctate scars.

Discussion: Dowling-Degos disease is a reticulate pigmentary disorder of the flexures associating prominent comedone-like lesions and pitted scars. Diagnosis is based on clinical and histopathological examination, which allows this entity to be differentiated from other reticulate pigmentary disorders. A literature review failed to provide any indication that PUVA therapy either aggravates or reveals Dowling-Degos disease, a finding which we feel merits mention.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Acitretin / therapeutic use
  • Genes, Dominant
  • Humans
  • Keratin-5 / genetics
  • Melanosis / complications*
  • Melanosis / diagnosis
  • Melanosis / genetics
  • Melanosis / pathology
  • Melanosomes / pathology
  • Middle Aged
  • PUVA Therapy / adverse effects*
  • Penetrance
  • Psoriasis / complications
  • Psoriasis / drug therapy*
  • Psoriasis / pathology
  • Ultraviolet Rays / adverse effects

Substances

  • KRT5 protein, human
  • Keratin-5
  • Acitretin