| Port-wine stain | |
|---|---|
| Classification and external resources | |
Mikhail Gorbachev has a prominent port-wine stain on his forehead. |
|
| ICD-10 | Q82.5 (ILDS Q82.510) |
| ICD-9 | 757.32 |
| OMIM | 163000 |
| DiseasesDB | 10384 |
| MedlinePlus | 001475 |
| eMedicine | derm/295 |
| MeSH | D019339 |
A port-wine stain or naevus flammeus is a vascular anomaly consisting of superficial and deep dilated capillaries in the skin which produce a reddish to purplish discoloration of the skin. They are so called for their colour, resembling that of port wine. It is part of the family of disorders known as vascular malformations, specifically an arteriovenous malformation.
The two terms are not always equated. Sometimes the term "naevus flammeus" is divided into two categories: port-wine stain and salmon patch.[1][2]
Port-wine stains are present at birth and 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. Early stains are usually flat and pink in appearance. As the child matures, the color may deepen to a dark red or purplish colour. In adulthood, thickening of the lesion or the development of small lumps may occur.[3]
PWS may be one of a group of symptoms and signs, in which case it is considered to be part of a syndrome such as Sturge-Weber syndrome or Klippel-Trenaunay-Weber syndrome.
Contents |
Nevus flammeus may be divided as follows:[4]
An association with RASA1 has been described.[5]
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.
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 have made the biggest impact on treatment, because they are the sole method of destroying the cutaneous capillaries without significant damage to the overlying skin.
The flashlamp pumped dye laser, a yellow light laser, has been the most successful at destroying stains in infants and young children.[6] The neodymium YAG laser is used to treat the nodules that may develop in some adult port-wine stains.
Treatment of infants with the flashlamp pumped dye laser generally produces marked improvement in appearance.[5]
However, complete disappearance is rare. In approximately 20%[7] of cases there may be no improvement at all. Stains on the face respond better than those on the trunk or limbs. Older stains may be more difficult to treat.
In the absence of successful treatment, hypertrophy (increased tissue mass) of the stains may produce deformity, loss of function (especially near the eye or mouth), bleeding, and increasing disfigurement. These complications are usually seen later in life. If the PWS is on the face or other highly visible part of the body, the presence of PWS can also cause emotional and social problems for the affected person because of their cosmetic appearance.
The incidence is 3–5 out of 1000 persons.[8][9]