Comparison between KTS and Parkes-Weber Syndrome3
KTS | Parkes-Weber Syndrome | |
---|---|---|
Cutaneous vascular malformation | Almost invariably tends to be dark; may be verrucous | Frequent; usually a pink capillary malformation |
Arteriovenous fistulas | Not significant | Invariablea |
Deep vein | Commona | Absent |
Lateral venous anomaly | Commona | Absent |
Gigantism | Usually disproportionate with soft-tissue thickening predominating; often giant toes present | Usually proportionate |
Lengthening of limb | Usually minor | Often minor |
Associated lesions | Common | Rare |
Lymphatics | Often hypoplastic | Usually hyperplastic |
Prognosis | Good; stable after childhood | May be progressive deterioration |
a Indicates signs present in our case.