Klippel-trenaunay syndrome
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2009; 19 (11): 729-731
em Inglês
| 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 (Mediterrâneo Oriental)
Assunto principal:
Fluxo Sanguíneo Regional
/
Tíbia
/
Deformidades Congênitas dos Membros
/
Síndrome de Klippel-Trenaunay-Weber
Tipo de estudo:
Relato de Casos
Limite:
Feminino
/
Humanos
Idioma:
Inglês
Revista:
J. Coll. Physicians Surg. Pak.
Ano de publicação:
2009
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