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Rhabdomyosarcoma (RMS) is the most common form of soft tissue sarcoma accounting for 4.5% of all cases of childhood cancer. It is the third most common extracranial solid tumor of childhood after Wilms tumor and neuroblastoma. RMS is a malignant tumor of mesenchymal origin and is included in the group of small blue, round cell tumors of childhood along with neuroblastoma, lymphoma and primitive neuroectodermal tumors (PNET).
see also Rhabdomyosarcoma of the Chest Wall and Paratesticular Rhabdomyosarcoma
Content in this topic is referenced in SCORE Rhabdomyosarcoma overview
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Last updated: October 24, 2018
Waldhausen, John, et al., editors. "Rhabdomyosarcoma." Pediatric Surgery NaT, American Pediatric Surgical Association, 2018. APSA Webapp, www.pedsurglibrary.com/apsa/view/Pediatric-Surgery-NaT/829140/all/Rhabdomyosarcoma.
Rhabdomyosarcoma. In: Waldhausen J, Powell D, Hirschl R, eds. Pediatric Surgery NaT. American Pediatric Surgical Association; 2018. https://www.pedsurglibrary.com/apsa/view/Pediatric-Surgery-NaT/829140/all/Rhabdomyosarcoma. Accessed May 26, 2019.
Rhabdomyosarcoma. (2018). In Waldhausen, J., Powell, D., & Hirschl, R. (Eds.), Pediatric Surgery NaT. Available from https://www.pedsurglibrary.com/apsa/view/Pediatric-Surgery-NaT/829140/all/Rhabdomyosarcoma
Rhabdomyosarcoma [Internet]. In: Waldhausen J, Powell D, Hirschl R, editors. Pediatric Surgery NaT. American Pediatric Surgical Association; 2018. [cited 2019 May 26]. Available from: https://www.pedsurglibrary.com/apsa/view/Pediatric-Surgery-NaT/829140/all/Rhabdomyosarcoma.
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T1 - Rhabdomyosarcoma
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Y1 - 2018/10/24/
BT - Pediatric Surgery NaT
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