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Poikiloderma
| Field | Value |
|---|---|
| image | File:Rothmund-Thomson syndrome.jpg |
| caption | People with varying manifestations of poikiloderma |
| specialty | dermatology |
Poikiloderma is a skin condition that consists of areas of hypopigmentation, hyperpigmentation, telangiectasias and atrophy. Poikiloderma of Civatte is most frequently seen on the chest or the neck, characterized by red colored pigment on the skin that is commonly associated with sun damage.
Types
- Poikiloderma vasculare atrophicans
- Poikiloderma of Civatte
- Hereditary sclerosing poikiloderma
Causes
- Congenital
- Rothmund-Thompson syndrome
- Dyskeratosis congenita
- Mendes da Costa syndrome
- Other hereditary causes
- Degos-Touraine syndrome
- Diffuse and macular atrophic dermatosis
- Hereditary sclerosing poikiloderma of weary
- Kindler syndrome
- Xeroderma pigmentosum
- Acquired
- Injury to cold, heat, ionizing radiation, exposure to sensitizing chemicals
- Lichen planus
- Dermatomyositis
- Lupus erythematosus
- Systemic sclerosis
- Cutaneous T cell lymphomas
Pathogenesis
The exact cause of poikiloderma of Civatte is unknown; however, extended sun exposure, namely the ultraviolet light emitted by the sun, is the primary factor.
Treatment
Albeit difficult, treatment of poikiloderma of Civatte involves the delivery of multiple wavelengths of intense pulsed light (IPL) to the affected area.
References
References
- (2011). "Laser and IPL Technology in Dermatology and Aesthetic Medicine". Springer Science & Business Media.
- American Osteopathic College of Dermatology [http://www.aocd.org/skin/dermatologic_diseases/Poikiloderma-of-Civatte.html "Dermatologic Disease Database"], ''aocd.org'', referenced July 22, 2011.
- PubMed.gov [https://www.ncbi.nlm.nih.gov/pubmed/11335804 "Treatment of poikiloderma of Civatte with an intense pulsed light source"], ''PubMed.gov'', referenced July 22, 2011.
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
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