एंजियोसारकोमा इसके अंग्रेजी अर्थ का उदाहरण

Lists of government ministers of Ghana Lymphangiosarcoma is a rare cancer which occurs in long-standing cases of primary or secondary lymphedema.

Although its name implies lymphatic origin, it is believed to arise from endothelial cells and may be more accurately referred to as angiosarcoma.

Lymphangiosarcoma may present as a purple discoloration or a tender skin nodule in the extremity, typically on the anterior surface.

Because of this change in clinical practice lymphedema is now a rarity following breast cancer treatment—and post-mastectomy lymphangiosarcoma is now vanishingly rare.

The pathogenesis of lymphangiosarcoma has not been resolved, however several vague mechanisms have been proposed.

The most successful treatment for lymphangiosarcoma is amputation of the affected limb if possible.

Malignant endothelial cells also commonly retain the antigen, so that CD31 immunohistochemistry can also be used to demonstrate both angiomas and angiosarcomas.

In computing, the computer configuration or preferences of the software Stewart–Treves syndrome, refers to a lymphangiosarcoma, a rare complication that forms as a result of chronic, long-standing lymphedema.

Although it most commonly refers to malignancies associated with chronic lymphedema resulting from mastectomy and/or radiotherapy for breast cancer, it may also describe lymphangiosarcomas that result from congenital and other causes of chronic secondary lymphedema.

Lymphangiosarcoma arising from cancer-related lymphedema has become much less common with better surgical techniques, radiation therapy, and conservative treatment.