منابع مشابه
Klippel-Trenaunay Syndrome
Figure 1. Asymmetric hypertrophy of the left arm and in particular the left first and second digit macrodactyly.
متن کاملThe Klippel-Trenaunay syndrome.
The Klippel-Trenaunay Syndrome is a triad of congenital anomalies characterized by a vascular naevus, varicose veins and hypertrophy of soft tissue and bone. A number of patients affected with this rare syndrome need amputation. In this paper the systemic problems, stump complications and prosthetic difficulties of four amputees with Klippel-Trenaunay syndrome are outlined. The period of follow...
متن کاملKlippel-Trenaunay Syndrome
A 30-month-old boy was brought in with the complaint of gradually increased size of his right lower extremity from birth. Soft tissue hypertrophy was detected in his right thigh, right dorsal region and scrotum. On the right leg, the skin had bluish discoloration. The leg was swollen and edeomatous. On plain radiography, we detected soft tissue hypertrophy, and there was length discrepancy betw...
متن کاملCME Klippel-Trenaunay Syndrome
Learning Objectives: After studying this article, the participant should be able to: 1. Define the triad of signs and symptoms that describe Klippel-Trenaunay syndrome. 2. Speculate on the various theories regarding its pathogenesis. 3. Discuss the necessary radiologic workup required to pursue appropriate management. 4. Restate the most common reasons for surgically treating this syndrome. 5. ...
متن کاملUltrasound-guided foam sclerotherapy in patients with Klippel-Trenaunay syndrome.
BACKGROUND Klippel-Trenaunay syndrome, a congenital disorder, is characterized by capillary malformation, varicosities and bony or soft tissue hypertrophy. Since there is no cure for this disorder, treatment is directed towards secondary prevention of venous hypertension and preservation of functional integrity of the legs. Elastic stockings are the mainstay of treatment and are indicated in al...
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ژورنال
عنوان ژورنال: Biomedical Journal of Scientific & Technical Research
سال: 2018
ISSN: 2574-1241
DOI: 10.26717/bjstr.2018.04.0001105