Stewart-Treves syndrome

Changed by Daniel J Bell, 11 Jul 2019

Updates to Article Attributes

Body was changed:

Stewart-Treves syndrome refers to an angiosarcoma seen in the setting of lymphoedema 1.

It was classically attributed to lymphoedemas induced by radical mastectomy to treat breast cancer. Nowadays, we know that it can arise in chronically lymphoedematous regions of any cause 2

The incidence is unknown, but studies have shown that it occurred in a rate between 0.03% and 0.45% in patients who survive at least 5 years after radical mastectomy 5,6.

Pathology

Etiology

It can arise from any cause of chronic lymphoedema 3,4:

PhysiopathologyPathophysiology

Chronic lymphoedema seems to induce a degree of local immunodeficiency that leads to oncogenesis 7.

Prognosis

Treatment and prognosis

The prognosis is very poor, because angiosarcomas are very aggressive tumors that frequently recur locally and often metastasize early.

  • -<p><strong>Stewart-Treves syndrome</strong> refers to an <a href="/articles/angiosarcoma">angiosarcoma</a> seen in the setting of <a href="/articles/lymphoedema">lymphoedema</a> <sup>1</sup>.</p><p>It was classically attributed to lymphoedemas induced by radical mastectomy to treat breast cancer. Nowadays, we know that it can arise in chronically lymphoedematous regions of any cause <sup>2</sup>. </p><p>The incidence is unknown, but studies have shown that it occurred in a rate between 0.03% and 0.45% in patients who survive at least 5 years after radical mastectomy <sup>5,6</sup>.</p><h5>Etiology</h5><p>It can arise from any cause of chronic lymphoedema <sup>3,4</sup>:</p><ul>
  • +<p><strong>Stewart-Treves syndrome</strong> refers to an <a href="/articles/angiosarcoma">angiosarcoma</a> seen in the setting of <a href="/articles/lymphoedema">lymphoedema</a> <sup>1</sup>.</p><p>It was classically attributed to lymphoedemas induced by <a title="Radical mastectomy" href="/articles/radical-mastectomy">radical mastectomy</a> to treat <a title="Breast cancer" href="/articles/breast-neoplasms">breast cancer</a>. Nowadays, we know that it can arise in chronically lymphoedematous regions of any cause <sup>2</sup>. </p><p>The incidence is unknown, but studies have shown that it occurred in a rate between 0.03% and 0.45% in patients who survive at least 5 years after radical mastectomy <sup>5,6</sup>.</p><h4>Pathology</h4><h5>Etiology</h5><p>It can arise from any cause of chronic lymphoedema <sup>3,4</sup>:</p><ul>
  • -<li>Milroy disease</li>
  • +<li><a title="Milroy disease" href="/articles/chronic-hereditary-lymphedema">Milroy disease</a></li>
  • -<li>filarial lymphoedema</li>
  • -<li>elephantiasis nostras verrucosa</li>
  • +<li><a title="Filarial infection" href="/articles/filariasis">filarial lymphoedema</a></li>
  • +<li><a title="Elephantiasis nostras verrucosa" href="/articles/elephantiasis-nostras-verrucosa">elephantiasis nostras verrucosa</a></li>
  • -</ul><h5>Physiopathology</h5><p>Chronic lymphoedema seems to induce a degree of local immunodeficiency that leads to oncogenesis <sup>7</sup>.</p><h5>Prognosis</h5><p>The prognosis is very poor, because angiosarcomas are very aggressive tumors that frequently recur locally and often metastasize early.</p><p> </p>
  • +</ul><h5>Pathophysiology</h5><p>Chronic lymphoedema seems to induce a degree of local immunodeficiency that leads to oncogenesis <sup>7</sup>.</p><h4>Treatment and prognosis</h4><p>The prognosis is very poor, because angiosarcomas are very aggressive tumors that frequently recur locally and often metastasize early.</p>

ADVERTISEMENT: Supporters see fewer/no ads

Updating… Please wait.

 Unable to process the form. Check for errors and try again.

 Thank you for updating your details.