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The three main features are nevus flammeus port-wine stainvenous and lymphatic malformations, and soft-tissue hypertrophy of the affected limb. The classical triad of Klippel-Trenaunay syndrome consists of: In some cases, port-wine stains capillary port wine type may be absent. Such cases are very rare and may be classified as "atypical Klippel—Trenaunay syndrome".

KTS can either affect blood vessels, lymph vessels, or both. The condition most commonly presents with a mixture of the two. Those with venous involvement experience increased pain and complications, such as venous ulceration in the lower extremities.

Those with large AVMs are at risk of formation of blood clots in the vascular lesion, which may migrate to the lungs pulmonary embolism. If there Clover von Thrombophlebitis large-volume blood flow through the lesion, "high-output Clover von Thrombophlebitis failure " may develop due to the inability of the heart to generate sufficient cardiac output. The birth defect affects men and women equally, and is not limited to any racial group.

It is not certain if it is genetic in nature, although testing is ongoing. Clover von Thrombophlebitis is disagreement as to how cases of KTS should be classified if there is an arteriovenous fistula present.

Clover von Thrombophlebitis is a complex syndrome, and no single treatment is applicable for everyone. At present, many of the symptoms may be treated, but there is no cure for Klippel—Trenaunay syndrome. Clover von Thrombophlebitis has been the most common treatment for KTS for several decades and while improvements have been made, the procedure is still considered invasive and has several risks associated with it.

More effective and less invasive treatment choices now exist for KTS patients and therefore debulking is generally only recommended as a last resort. Debulking operations can result in major deformities and also leave patients with permanent nerve damage.

Mayo Clinic has reported the largest experience in managing KTS with major surgery. In 39 years at Mayo clinic the surgery team evaluated consecutive cases of KTS, of which only All the procedures demonstrated high recurrence rate in the follow-up.

Mayo clinic studies demonstrate that primary surgical management of KTS has limitations and non-surgical approaches need to be developed in order to offer a better quality of life for these patients. Major surgery including amputation and debulking surgery does not seem to offer any benefit on a long-term basis. Sclerotherapy is a treatment for specific veins and vascular malformations in the affected area. It involves the injection of a chemical into the abnormal veins to cause thickening and obstruction of the targeted click here. Such treatment may allow normal blood flow to resume.

It is a non-surgical medical procedure and is not nearly as invasive as debulking. Ultrasound guided foam sclerotherapy is the state of the art new treatment which could potentially close many large vascular malformations. Compression therapies are finding more use as of the last ten years. This can cause pain, swelling, inflammations, and in some cases, even ulceration and infection.

Among older children and adults, compression garments can be used to alleviate almost all of these, and Clover von Thrombophlebitis combined with elevation of the affected area and proper management, can result in a comfortable lifestyle for the patient without any surgery.

Compression garments are also used lately after a debulking procedure Clover von Thrombophlebitis maintain the results Clover von Thrombophlebitis the procedure.

For early treatment of infants and toddlers with KTS, custom compression garments are impractical because of the rate of growth. When children may benefit from compression therapies, wraps and lymphatic massage may be used. While compression garments or therapy are not appropriate for everyone, they are relatively cheap compared to surgeryand have few side-effects.

Possible side-effects include a slight risk that the fluids may simply be displaced to an undesirable location e. From Wikipedia, the free encyclopedia. This Varizen Teer is empty. You can help by adding to it. Archived from the original check this out Clover von Thrombophlebitis 4, Retrieved May Clover von Thrombophlebitis, Clinical Dermatology 10th ed.

Indian Dermatology Online Journal. Indian journal of dermatology, venereology and leprology. Archived from the original PDF on Clover von Thrombophlebitis 9, Cytogenetic and Genome Research.

Journal of Medical Genetics. American Journal of Medical Genetics. Brooklyn writer Carla Sosenko shares facts about condition". New York Daily News. British Journal of Dermatology. Congenital abnormality syndromes Q87 Bardet—Biedl syndrome Laurence—Moon syndrome. Retrieved from " https: Clover von Thrombophlebitis diseases Syndromes affecting the vascular Infobox medical condition Articles to be expanded from July All articles Clover von Thrombophlebitis be expanded Articles with empty sections from July All articles with empty sections Articles using small message boxes All articles with unsourced statements Articles with unsourced statements from October Views Read Edit View history.

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