Literature DB >> 22007646

Adult-onset dyschromatoses.

V Vachiramon1, K Thadanipon, P Rattanakaemakorn.   

Abstract

The dyschromatoses are a group of pigmentary disorders characterized clinically by mixed and often guttate hypopigmentend and hyperpigmented lesions. There are many conditions that present with dyschromatosis, including genodermatoses, inflammatory skin diseases, infections, drug and chemical use, and nutritional disorders. Some conditions have extracutaneous features. In this article, we describe the dyschromatoses with typical onset in adulthood. Most diseases in this group are acquired conditions. To organize the various acquired dyschromatoses, we have categorized them into those with a history of chemical exposure, drug exposure or dermatological procedures, and those without a history of such exposure. In contrast to the genetic dyschromatoses, some acquired dyschromatoses are preventable and treatable. We hope this review will serve as a guide for dermatologists to the recognition and treatment of these conditions. © The Author(s). CED
© 2011 British Association of Dermatologists.

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Year:  2011        PMID: 22007646     DOI: 10.1111/j.1365-2230.2011.04161.x

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN: 0307-6938            Impact factor:   3.470


  1 in total

1.  Dyschromatosis symmetrica hereditaria of late onset?

Authors:  Caroline Balvedi Gaiewski; Sergio Zuneda Serafini; Betina Werner; Janyana M D Deonizio
Journal:  Case Rep Dermatol Med       Date:  2014-02-04
  1 in total

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