Sneddon-Wilkinson disease treated with etanercept: report of two cases

Clin Exp Dermatol. 2009 Apr;34(3):347-51. doi: 10.1111/j.1365-2230.2008.02905.x. Epub 2008 Aug 9.

Abstract

Sneddon-Wilkinson disease (SWD), also known as subcorneal pustular dermatosis, is a rare, chronic eruption that is often difficult to treat, particularly in patients who do not respond to or cannot tolerate dapsone. Few case reports exist of patients with SWD treated with antitumour necrosis factor-alpha therapy. We report two patients with SWD refractory to numerous treatments, who responded to etanercept (in combination with low-dose acitretin in one case).

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Aged
  • Dermatologic Agents / therapeutic use*
  • Etanercept
  • Female
  • Humans
  • Immunoglobulin G / therapeutic use*
  • Male
  • Middle Aged
  • Receptors, Tumor Necrosis Factor / therapeutic use*
  • Skin Diseases, Vesiculobullous / drug therapy*
  • Skin Diseases, Vesiculobullous / pathology
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors

Substances

  • Dermatologic Agents
  • Immunoglobulin G
  • Receptors, Tumor Necrosis Factor
  • Tumor Necrosis Factor-alpha
  • Etanercept