This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Go to /pro/cpd-dashboard page

This page is worth 0.05 CPD credits. CPD dashboard

Go to /account/subscription-details page

This page is worth 0.05 CPD credits. Upgrade to Pro

Complications

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Lymphangiosarcoma is a rare malignant tumour which occurs in long standing cases of primary or acquired lymphoedema. It involves either the upper or lower lymphoedematous extremities but is most common in the upper extremity.

Lymphangiosarcoma is classically seen in upper extremity lymphedema occurring after mastectomy (Stewart-Treves syndrome) (1).

This sarcoma first appears as a bruise mark, a purplish discolouration or a tender skin nodule in the extremity, typically on the the anterior surface. It progresses to an ulcer with crusting, and finally to an extensive necrosis involving the skin and subcutaneous tissue.

It metastasises widely.

No effective therapy is reported.

Reference:


Related pages

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.