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Klippel-Trenaunay syndrome.
Rasheed, Rashid; Rahim, Muhammad Kashif; Uddin, Najam.
Afiliação
  • Rasheed R; Department of Nuclear Medicine, Multan Institute of Nuclear Medicine and Radiotherapy, Nishtar Hospital, Multan.
J Coll Physicians Surg Pak ; 19(11): 729-31, 2009 Nov.
Article em En | MEDLINE | ID: mdl-19889273
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Klippel-Trenaunay-Weber Limite: Adult / Female / Humans Idioma: En Revista: J Coll Physicians Surg Pak Assunto da revista: MEDICINA Ano de publicação: 2009 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Klippel-Trenaunay-Weber Limite: Adult / Female / Humans Idioma: En Revista: J Coll Physicians Surg Pak Assunto da revista: MEDICINA Ano de publicação: 2009 Tipo de documento: Article