Port Wine Stains - Indentification & Treatment of the "Vascular" Birthmark
A Guide to Identification, Disease and Treatment of Port Wine Stains
By Christine Cadena, published Apr 11, 2006
Published Content: 3,262 Total Views: 1,922,593 Favorited By: 79 CPs
The cause and origin of a port wine stain is unknown. What is known is the condition is congenital but not hereditary and does not appear to be related to any condition of pregnancy nor trauma to the mother. What is also known is that the stains appear as irregular patches of light or pale pink discoloration which gradually deepen in color with progression of time. Unlike standard birthmarks, port wine stains will enlarge and grow as the skin grows. Found usually on the face, neck, shoulders or chest, the patches, as they grow, will not only darken in color but may also transist from a smooth marking to a marking demonstrating a more thick and pebbled appearance. The malformation is the result of an over abundance of tiny blood vessels in the upper levels of the skin; blood vessels connecting veins and arteries. Because the growth and location of the stains is relatively consistent, medical science has identified conditions and diseases which may impact the patient’s health status.
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Takeaways
- Port Wine Stains are considered one of three types of "vascular" birthmarks.
- Sturge-Weber Syndrome can lead to blindness if not treated.
- Port Wine Stains affect three out of every 1000 births. The origin is unknown.
Did You Know?
Port Wine Stains can be fatal, in rare cases, if syndromes associated with the condition are left undiagnosed or untreated.
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