Rhabdomyosarcoma Support Group

It can be a cardiac manifestation of tuberous sclerosis.

The two most common forms of rhabdomyosarcoma (which is a relatively rare form of cancer) are embryonal rhabdomyosarcoma, and alveolar rhabdomyosarcoma. In the former, the cancer cells resemble those of a typical 6-to-8-week embryo. In the latter, they resemble those of a typical 10-to-12-week embryo. The former is more common in younger children, and the latter in older children and teenagers.

When rhabdomyosarcoma is suspected, tests will be run for blood, muscle, and marrow.

Diagnosis of rhabdomyosarcoma depends on recognition of differentiation toward skeletal muscle cells. The protein myo D1 is a protein normally found in developing skeletal muscle cells which disappears after the muscle matures and becomes innervated by a nerve. Thus, myo D1 is not found in normal skeletal muscle and serves as a useful histochemical marker of rhabdomyosarcoma.

Treatment for rhabdomyosarcoma consists of chemotherapy, radiation therapy and sometimes surgery. Surgery to remove the tumor is often difficult or impossible because the tumor is usually embedded deep within the tissue, leaving it difficult to reach. If a tumor presents itself in the extremities, amputation is often necessary to improve survival.

If there is no evidence of metastasis, surgery combined with chemotherapy and radiation offer the best prognosis. Patients whose tumors have metastisized have a poor chance for long-term survival. In patients who began treatment before metastasis, the prognosis is better, although the disease is generally incurable because the tumors that cannot be surgically removed tend to spread.