Advanced Search

Home > Journals > International Angiology > Past Issues > International Angiology 2006 September;25(3) > International Angiology 2006 September;25(3):322-6



A Journal on Angiology

Official Journal of the International Union of Angiology, the International Union of Phlebology and the Central European Vascular Forum
Indexed/Abstracted in: BIOSIS Previews, Current Contents/Clinical Medicine, EMBASE, PubMed/MEDLINE, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 0,899

Frequency: Bi-Monthly

ISSN 0392-9590

Online ISSN 1827-1839


International Angiology 2006 September;25(3):322-6

    Case reports

Klippel-Trenaunay syndrome: an unusual cause of pulmonary embolism

Skourtis G. 1, Lazoura O. 2, Panoussis P. 1, Livieratos L. 2

1 Department of Vascular Surgery, KAT General Hospital, Athens, Greece
2 Department of Radiology, KAT General Hospital, Athens, Greece

A 36-year-old female patient was admitted to the emergency department of our hospital with symptoms and signs of pulmonary embolism. Further evaluation established the diagnosis and anticoagulant therapy was immediately started. Physical examination revealed left lower extremity edema, prominent varicose veins, greater length of the involved limb and a capillary malformation extending from the lower abdomen down to the left knee. The diagnosis of Klippel-Trenaunay syndrome (KTS) was suspected and a color duplex scan was next performed revealing derangements in the lower extremity venous system including deep venous thrombosis. KTS is a congenital anomaly characterized by capillary malformation, extensive varicosities and limb hypertrophy. Anomalies of the deep and perforator venous system coexist and predispose to thromboembolic events. Pulmonary embolism is infrequently encountered in the setting of this syndrome.

language: English


top of page