Paget-Schroetter syndrome associated with FV : Q(506) and prothrombin 20210A - A case report


Sayinalp N. , Ozcebe O., Kirazli S., Dogan R., Dundar S., Gurgey A.

ANGIOLOGY, cilt.50, sa.8, ss.689-692, 1999 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 50 Konu: 8
  • Basım Tarihi: 1999
  • Doi Numarası: 10.1177/000331979905000811
  • Dergi Adı: ANGIOLOGY
  • Sayfa Sayıları: ss.689-692

Özet

Effort thrombosis of the axillary-subclavian vein (Paget-Schroetter syndrome) develops usually secondary to heavy arm exertion. An underlying chronic venous compressive anomaly at the thoracic outlet or intimal damage of the axillary vein following forceful hyperabduction, external rotation of the shoulder joint has been proposed to explain the pathophysiology of this thrombosis. This condition is usually not attributed to an underlying hypercoagulability such as deficiency of natural coagulation inhibitors. Here, the authors present a case with thrombosis of the axillary-subclavian vein following an effort, with factor V Leiden and prothrombin 20210A mutations. Both factor V Leiden and the genetic variant in the prothrombin gene have been shown to confer an increased risk for venous thrombosis. Although rare, effort thrombosis may develop in a patient with hereditary thrombophilia, so laboratory evaluation should include the common causes of thrombosis.