Lymphangiosarcoma of the arm presenting with lymphedema in a woman 16 years after mastectomy: A case report

Yasir J. Sepah; Masood Umer; Asim Qureshi; Shaista Khan

doi:10.4076/1757-1626-2-6887

Lymphangiosarcoma of the arm presenting with lymphedema in a woman 16 years after mastectomy: A case report

Yasir J. Sepah, Masood Umer, Asim Qureshi, Shaista Khan

Department of Surgery, Medical College, Pakistan

Research output: Contribution to journal › Article › peer-review

4 Citations (Scopus)

Abstract

Lymphangiosarcoma following breast cancer is a relatively rare entity, with around 300 cases so far reported worldwide. Affecting the long term survivors of breast cancer, lymphangiosarcoma (Stewart-Traves Syndrome) has a high mortality rate. Since lympedema following radical mastectomy or axillary clearance and radiotherapy seems to be the main predisposing factor, further research regarding modifications in the surgical technique of axillary nodes dissection as well as the development of new chemotherapeutic agents effective in lymphangiosarcoma are required.

Original language	English
Article number	6887
Journal	Cases Journal
Volume	2
Issue number	9
DOIs	https://doi.org/10.4076/1757-1626-2-6887
Publication status	Published - Sept 2009

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abstract = "Lymphangiosarcoma following breast cancer is a relatively rare entity, with around 300 cases so far reported worldwide. Affecting the long term survivors of breast cancer, lymphangiosarcoma (Stewart-Traves Syndrome) has a high mortality rate. Since lympedema following radical mastectomy or axillary clearance and radiotherapy seems to be the main predisposing factor, further research regarding modifications in the surgical technique of axillary nodes dissection as well as the development of new chemotherapeutic agents effective in lymphangiosarcoma are required.",

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AU - Khan, Shaista

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N2 - Lymphangiosarcoma following breast cancer is a relatively rare entity, with around 300 cases so far reported worldwide. Affecting the long term survivors of breast cancer, lymphangiosarcoma (Stewart-Traves Syndrome) has a high mortality rate. Since lympedema following radical mastectomy or axillary clearance and radiotherapy seems to be the main predisposing factor, further research regarding modifications in the surgical technique of axillary nodes dissection as well as the development of new chemotherapeutic agents effective in lymphangiosarcoma are required.

AB - Lymphangiosarcoma following breast cancer is a relatively rare entity, with around 300 cases so far reported worldwide. Affecting the long term survivors of breast cancer, lymphangiosarcoma (Stewart-Traves Syndrome) has a high mortality rate. Since lympedema following radical mastectomy or axillary clearance and radiotherapy seems to be the main predisposing factor, further research regarding modifications in the surgical technique of axillary nodes dissection as well as the development of new chemotherapeutic agents effective in lymphangiosarcoma are required.

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Lymphangiosarcoma of the arm presenting with lymphedema in a woman 16 years after mastectomy: A case report

Abstract

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