Literature DB >> 20548927

Chemical Leukoderma Improved by Low-dose Steroid Pulse Therapy.

Jae Yoon Jung1, Kkot Bora Yeom, Hee Chul Eun.   

Abstract

Chemical leukoderma occurs due to the toxic effect of a specific chemical preceding allergic contact dermatitis. The mechanism is either destruction or inhibition of melanocytes by the offending substance. Clinicohistopathologically, no absolute criteria can differentiate chemical leukoderma from vitiligo. However, chemical leukoderma can be diagnosed clinically by a history of repeated exposure to a known or suspected depigmenting agent at the primary site. There is no agreed treatment guideline for chemical leukoderma. We report a healthy 51-year-old man who had multiple hypopigmented macules and patches on his face, neck, arms and legs after exposure to occupationally related chemicals. The lesions were recalcitrant to topical corticosteroids, but they showed much improvement after 3 cycles of systemic steroid pulse therapy. We suggest this therapy may be a good treatment option for chemical leukoderma.

Entities:  

Keywords:  Chemical leukoderma; Systemic steroid; Vitiligo

Year:  2010        PMID: 20548927      PMCID: PMC2883439          DOI: 10.5021/ad.2010.22.2.241

Source DB:  PubMed          Journal:  Ann Dermatol        ISSN: 1013-9087            Impact factor:   1.444


  11 in total

Review 1.  A critical appraisal of vitiligo etiologic theories. Is melanocyte loss a melanocytorrhagy?

Authors:  Yvon Gauthier; Muriel Cario Andre; Alain Taïeb
Journal:  Pigment Cell Res       Date:  2003-08

Review 2.  A review and a new hypothesis for non-immunological pathogenetic mechanisms in vitiligo.

Authors:  Maria Lucia Dell'anna; Mauro Picardo
Journal:  Pigment Cell Res       Date:  2006-10

3.  Chemical leucoderma: a clinico-aetiological study of 864 cases in the perspective of a developing country.

Authors:  S Ghosh; S Mukhopadhyay
Journal:  Br J Dermatol       Date:  2008-09-06       Impact factor: 9.302

4.  Depigmentation caused by phenolic detergent germicides.

Authors:  G Kahn
Journal:  Arch Dermatol       Date:  1970-08

5.  Oral dexamethasone pulse treatment for vitiligo.

Authors:  S Radakovic-Fijan; A M Fürnsinn-Friedl; H Hönigsmann; A Tanew
Journal:  J Am Acad Dermatol       Date:  2001-05       Impact factor: 11.527

6.  The efficacy of low-dose oral corticosteroids in the treatment of vitiligo patients.

Authors:  S M Kim; H S Lee; S K Hann
Journal:  Int J Dermatol       Date:  1999-07       Impact factor: 2.736

7.  Leukoderma following occupational allergic contact dermatitis.

Authors:  A Kumar; S Freeman
Journal:  Contact Dermatitis       Date:  1999-08       Impact factor: 6.600

8.  Occupational depigmentation due to 4-tertiarybutyl catechol (TBC).

Authors:  G A Gellin; P A Possick; I H Davis
Journal:  J Occup Med       Date:  1970-10

Review 9.  On the etiology of contact/occupational vitiligo.

Authors:  Raymond E Boissy; Prashiela Manga
Journal:  Pigment Cell Res       Date:  2004-06

10.  Guideline for the diagnosis and management of vitiligo.

Authors:  D J Gawkrodger; A D Ormerod; L Shaw; I Mauri-Sole; M E Whitton; M J Watts; A V Anstey; J Ingham; K Young
Journal:  Br J Dermatol       Date:  2008-11       Impact factor: 9.302

View more
  1 in total

1.  Chemical leukoderma induced by dimethyl sulfate.

Authors:  Maya Valeska Gozali; Jia-An Zhang; Fei Yi; Bing-Rong Zhou; Dan Luo
Journal:  An Bras Dermatol       Date:  2016 Sep-Oct       Impact factor: 1.896

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.