Ann Dermatol.  2015 Feb;27(1):92-94. 10.5021/ad.2015.27.1.92.

Adult Onset Dyschomatosis Universalis

Affiliations
  • 1Department of Dermatology, School of Medicine, Chosun University, Gwangju, Korea. derm75@chosun.ac.kr

Abstract

No abstract available.


MeSH Terms

Adult*
Humans

Figure

  • Fig. 1 (A) Multiple pinhead to rice sized mottled hypopigmented macules with diffuse hyperpigmented patches. (B) A closer view. (C) A biopsy specimen taken from a hyperpigmented lesion on the abdomen showed increased abundant melanin pigments in the epidermis with a normal number and distribution of melanocytes (H&E, ×200; left inset: Fontana Masson, ×200; right inset: melanoma antigen recognized by T cells 1 [MART-1] ×200). (D) A hypopigmented macule showed reduced amount of melanin pigments in the lesion area (H&E, ×200; left inset: Fontana Masson, ×200; right inset: MART-1, ×200).


Reference

1. Urabe K, Hori Y. Dyschromatosis. Semin Cutan Med Surg. 1997; 16:81–85.
Article
2. Kim YJ, Oh CN, Chung BS, Choi KC. Two cases of dyschromatosis universalis. Korean J Dermatol. 1992; 30:928–931.
3. Rycroft RJ, Calnan CD, Wells RS. Universal dyschromatosis, small stature and high-tone deafness. Clin Exp Dermatol. 1977; 2:45–48.
Article
4. Shono S, Toda K. Universal dyschromatosis associated with photosensitivity and neurosensory hearing defect. Arch Dermatol. 1990; 126:1659–1660.
Article
5. Kim NS, Im S, Kim SC. Dyschromatosis universalis hereditaria: an electron microscopic examination. J Dermatol. 1997; 24:161–164.
Article
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