INVERSE KLIPPEL-TRENAUNAY SYNDROME
نویسندگان
چکیده
منابع مشابه
Mild form of inverse Klippel-Trenaunay syndrome?
To cite: Queirós G, Diamantino F, Lopes MJ. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2013-009188 DESCRIPTION Klippel-Trenaunay syndrome (KTS) is defined by a coexistence of nevus flammeus and overgrowth of one or more limbs. Remarkably, however, deficient growth of an affected limb may likewise be noted. It has been speculated that either a ‘plus’ or ‘minu...
متن کاملKlippel-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. ...
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ژورنال
عنوان ژورنال: Revista Paulista de Pediatria
سال: 2020
ISSN: 1984-0462,0103-0582
DOI: 10.1590/1984-0462/2020/38/2020091