|Classification and external resources|
Mikhail Gorbachev has a prominent port-wine stain on his forehead.
|ICD-10||Q82.5 (ILDS Q82.510)|
Port-wine stains ordinarily persist throughout life. The area of skin affected grows in proportion to general growth. Port-wine stains occur most often on the face but can appear anywhere on the body, particularly on the neck and upper trunk. Early stains are usually flat and pink in appearance. As the child matures, the color may deepen to a dark red or purplish color. In adulthood, thickening of the lesion or the development of small lumps may occur.They are called port wine for their reddish color.
Nevus flammeus may be divided as follows:
A physician can usually diagnose a port wine stain based entirely upon the history and appearance. In unusual cases, a skin biopsy may be needed to confirm the diagnosis. Depending on the location of the birthmark and other associated symptoms, a physician may choose to order a measurement of intraocular pressure or X-ray of the skull.
A MRI scan of the brain may be performed (under anesthesia) on infants who have a Port-wine stain in the head area. This is done to check for signs of Sturge-Weber syndrome.
If the Port-wine stain is inside the mouth, a physician may check the insides of a newborn baby's throat with a scope to see if there are any changes (growths) other than just the color.
If the Port-wine stain is around the eye or on the eyelid, a referral may be made to an optometrist or ophthalmologist for a test of the ocular pressures in that eye. If swelling occurs in the Port-wine stain, it may cause vision problems and blindness.
Many treatments have been tried for port-wine stains including freezing, surgery, radiation, and tattooing; port-wine stains can also be covered with cosmetics. Lasers may be able to destroy the capillaries without significant damage to the overlying skin. Lasers and other light sources may therefore be able to reduce the redness of stains, although there is not enough evidence to recommend one form over another. For most people in trials of pulsed dye laser, more than 25% of the redness was reduced by laser after 1 to 3 treatments. Adverse effects were rare in these trials, although some people had changes to the color of the skin, especially Chinese people with darker skin. There can be pain, crusting and blistering in the two weeks after treatment. The trials only followed people for six months, so longterm outcomes are not known. Up to 10 treatments may be necessary for improvement, but complete removal may not result.
Treatment is generally given before one year of age. However, as it is recommended to be performed under anesthesia (15 minutes) on small children, it is not always possible to get frequent treatments. For example in Finland a child gets treated 2-3 times per year, resulting in a target of "being ready before school age" (7 years).
After the laser treatment the skin is filled with black marks, the size of a pen. This is due to the laser instrument's size. The black marks will disappear within 1-3 weeks. The treated area can be sore and swollen for a couple of days.
In the absence of successful treatment, hypertrophy (increased tissue mass) of the stains may cause problems later in life, such as loss of function (especially if the stain near the eye or mouth), bleeding, and increasing disfigurement. Lesions on or near the eyelid can be associated with glaucoma. If the port-wine stain is on the face or other highly visible part of the body, its presence can also cause emotional and social problems for the affected person.
- Primary Care Dermatology Society, UK. "Port-wine stain". Clinical Guidance. Primary Care Dermatology Society, UK. Retrieved 8 July 2013.
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- James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. Page 582–3. ISBN 0-7216-2921-0.
- Shirley, Matthew D.; Tang, Hao; Gallione, Carol J.; Baugher, Joseph D.; Frelin, Laurence P.; Cohen, Bernard; North, Paula E.; Marchuk, Douglas A.; Comi, Anne M.; Pevsner, Jonathan (8 May 2013). "Sturge–Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in". New England Journal of Medicine. doi:10.1056/NEJMoa1213507.
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- Alper, JC; Holmes, LB (1983). "The incidence and significance of birthmarks in a cohort of 4,641 newborns". Pediatric dermatology 1 (1): 58–68. doi:10.1111/j.1525-1470.1983.tb01093.x. PMID 6679890.
- Information about Port Wine Stains from Children's Hospital, Seattle.
- Sturge–Weber Syndrome Community