Rhabdomyosarcoma natural history, complications and prognosis: Difference between revisions
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==Overview== | ==Overview== |
Revision as of 16:05, 10 September 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Suveenkrishna Pothuru, M.B,B.S. [2]
Overview
Common complication of rhabdomyosarcoma include metastasis to lung, bone marrow, and bone. Rhabdomyosarcoma is associated with a 5 year survival rate of 72%. The presence of metastasis is associated with a particularly poor prognosis. The embryonal type rhabdomyosarcoma is associated with the most favorable prognosis. Orbital and genitourinary tract rhabdomyosarcomas have the most favorable prognosis.
Complications
- Rhabdomyosarcoma may cause metastasis to other organs.
- Lung is the most common location for metastatic disease.[1]
- Other common sites of metastasis are bone marrow and bones.
Prognosis
- Rhabdomyosarcoma is associated with a 5 year survival rate of 72%.
- The presence of metastasis is associated with a particularly poor prognosis among patients with rhabdomyosarcoma. The 5 year event free survival rate is less than 30%.
- Embryonal type rhabdomyosarcoma is associated with the most favorable prognosis.
- Prognosis varies with location of tumor- orbital and genitourinary tract rhabdomyosarcomas have the most favorable prognosis.