Klippel-trenaunay syndrome
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2009; 19 (11): 729-731
en Inglés
| IMEMR
| ID: emr-102165
ABSTRACT
Klippel-Trenaunay Syndrome [KTS] is a rare, congenital, vascular disorder affecting one or more limbs. Originally, it was defined as a triad including port wine stain, varicose veins and bony and soft tissue hypertrophy. We present a case of a 20-year-old female who walked with a limp. Because of swelling of right leg she was sent for Doppler study which picked up dilated arteries and increased blood flow velocity. The impression of KTS was further strengthened by unique nuclear medicine and radiological findings:
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Flujo Sanguíneo Regional
/
Tibia
/
Deformidades Congénitas de las Extremidades
/
Síndrome de Klippel-Trenaunay-Weber
Tipo de estudio:
Informe de Casos
Límite:
Femenino
/
Humanos
Idioma:
Inglés
Revista:
J. Coll. Physicians Surg. Pak.
Año:
2009
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