Poikiloderma
| Poikiloderma | |
|---|---|
 | |
| 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.[1]
Types
Causes
- Congenital
- 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.[2]
Diagnosis
This section is empty. You can help by adding to it. (July 2018)
Treatment
Albeit difficult, treatment of poikiloderma of Civatte involves the delivery of multiple wavelengths of intense pulsed light (IPL) to the affected area.[3]
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.
Cover photo is available under {{::mainImage.info.license.name || 'Unknown'}} license.
Cover photo is available under {{::mainImage.info.license.name || 'Unknown'}} license.
Credit:
(see original file).
