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- www.mayoclinic.org
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Dec 20, 2023 · Rarely, rhabdomyosarcoma has been linked to genetic syndromes that are passed from parents to children. These include neurofibromatosis 1, Noonan syndrome, Li-Fraumeni syndrome, Beckwith-Wiedemann syndrome and Costello syndrome.
Rhabdomyosarcoma is a rare soft tissue cancer that typically affects children and teenagers but can also affect adults. You can develop rhabdomyosarcoma anywhere in your body, but it usually affects muscles in your arms, legs, head and neck, and abdomen (belly).
Rhabdomyosarcoma is a type of cancer. It starts in cells that grow into skeletal muscle cells. The cells are called rhabdomyoblasts. Skeletal muscles control all of a person’s voluntary muscle movements. The cancer is most common in children under age 10, but it is rare.
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Apr 8, 2022 · Treatment of children with rhabdomyosarcoma often includes chemotherapy, radiation therapy, and surgery. Learn about the signs, tests to diagnose, survival, treatment, and clinical trials for children with rhabdomyosarcoma in this expert-reviewed summary.
Rhabdomyosarcoma in children is a rare cancer but is the most common type of soft tissue sarcoma (a tumor that is malignant, or that spreads). Rhabdomyosarcomas are comprised of primitive muscle cells.
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Childhood rhabdomyosarcoma is a soft tissue malignant tumor of mesenchymal origin. It accounts for approximately 2.7% of cancer cases among children aged 0 to 14 years and 1.4% of the cases among adolescents and young adults aged 15 to 19 years. [ 2]
Rhabdomyosarcoma is the most common type of soft tissue sarcoma in children. About 350 new cases are diagnosed each year in the United States. More than 70% of children with rhabdomyosarcoma that has not spread survive long-term.
This rare cancer is most common in children under age 10. It can start anywhere in the body. The most common places are: Head and neck, such as near an eye, in the throat or in the sinuses. Urinary and reproductive organs, such as the bladder, prostate gland or any female organs. Arms and legs. Chest and belly (abdomen)
Feb 12, 2024 · RMS is the most common soft tissue sarcoma diagnosed in children; only 1% to 2% of these cancers are found in adults. The etiology and risk factors remain largely unknown. Most cases of rhabdomyosarcoma are sporadic; however, the disease can be associated with familial syndromes.
Rhabdomyosarcoma (rhab· do· myo· sar· co· ma) is a rare childhood cancer that typically begins in a muscle. It can be cured, but requires complex treatment that may include radiation, surgery and chemotherapy.
