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Case Report

Open Access

Debilitating Darier’s disease

  • DAVID W. BRODELL1
  • LAWRENCE E. FRISCH2
  • ROBERT T. BRODELL3

1Washington University in St. Louis

2Northeastern Ohio Universities College of Medicine

3Northeastern Ohio Universities College of Medicine Rootstown, Ohio Case Western Reserve School of Medicine Cleveland, Ohio University of Rochester School of Medicine and Dentistry Rochester

DOI: 10.22514/SV21.042007.8 Vol.2,Issue 1,April 2007 pp.33-34

Published: 20 April 2007

*Corresponding Author(s): ROBERT T. BRODELL E-mail: rtb@neoucom.edu

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Abstract

Darier’s disease is an inherited dermatitis that is due to a mutation in the ATP2A2 gene. This mutation causes disrupted signaling within cells and leads to a skin condition that is resistant to many dermatologic treatments. Though serious complications are rare, Darier’s disease can result in bacterial sepsis and Kaposi’s varicelliform eruption. In some families seizure disorders are linked to Darier’s disease. There is also a paraneoplastic variant that could be considered in patients without a family history of Darier’s disease. This article reports a case with typical verrucous masses and waxy papules which, over twenty years, became disabling. Symptoms included pruritus and foul odor and were relieved, along with the keratotic rash, utilizing systemic treatment with acitretin though the condition recurred rapidly when treatment was interrupted. Darier’s disease must be considered when patients present with hyperkeratotic lesions that are resistant to usual forms of therapy for inflammatory dermatoses.

Key words

Darier’s Disease, ace-tretin, inherited dermatoses.

Cite And Share

DAVID W. BRODELL,LAWRENCE E. FRISCH,ROBERT T. BRODELL. Debilitating Darier’s disease. Signa Vitae. 2007. 2(1);33-34.

References

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