Paget–Schroetter disease

Paget–Schrotter disease
Other names	Paget–von Schrötter disease
Anterior view of right upper limb and thorax
Specialty	Vascular surgery
Named after	James Paget Leopold von Schrötter

Paget–Schroetter disease (which evolved from a venous thoracic outlet syndrome) is a form of upper extremity

The condition is relatively rare.[2] It usually presents in young and otherwise healthy patients, and also occurs more often in males than females. The syndrome also became known as "effort-induced thrombosis" in the 1960s,^[3] as it has been reported to occur after vigorous activity,^[4] though it can also occur due to anatomic abnormality such as clavicle impingement^[5] or spontaneously. It may develop as a sequela of thoracic outlet syndrome. It is differentiated from secondary causes of upper extremity thrombosis caused by intravascular catheters.^[4] Paget–Schroetter syndrome was described once for a viola player who suddenly increased practice time 10-fold, creating enough repetitive pressure against the brachiocephalic and external jugular veins to cause thrombosis.^[6]

Symptoms may include sudden onset of pain, warmth, redness, blueness and swelling in the arm. Diagnosis is usually confirmed with an ultrasound.^[7] These DVTs have the potential to cause a pulmonary embolism.^[8]

Diagnosis

Duplex ultrasonography MR Venography^{[citation needed]}

Prevention

Prevention of Paget–Schroetter disease can be accomplished by gradual increases in activity and by avoiding strenuous upper extremity activity.^[9]

Treatment

The traditional treatment for thrombosis is the same as for a lower extremity DVT, and involves systemic

The condition is named after two men. James Paget^[13] first proposed the idea of venous thrombosis causing upper extremity pain and swelling,^[14] and Leopold von Schrötter later linked the clinical syndrome to thrombosis of the axillary and subclavian veins.^[15]

References