Embryonal rhabdomyosarcoma
Embryonal rhabdomyosarcoma (ERMS) is a rare cancer that forms in muscle tissue. It is a type of soft tissue sarcoma that usually occurs in children.
Overview[edit | edit source]
ERMS is a disease in which malignant (cancer) cells form in muscle tissue. ERMS is a type of rhabdomyosarcoma, a cancer of the soft tissue. Rhabdomyosarcoma is the most common type of soft tissue sarcoma in children. It can begin in many places in the body.
Symptoms[edit | edit source]
There are no specific symptoms for ERMS. However, an unusual lump or swelling, pain, fever, or illness that doesn’t go away can be signs of ERMS. Other conditions can cause the same symptoms, so it is important to consult a doctor if any of these occur.
Diagnosis[edit | edit source]
Tests that examine the body and the area where the tumor is found are used to detect and diagnose ERMS. These tests may include imaging tests, laboratory tests, and biopsies.
Treatment[edit | edit source]
Treatment for ERMS may include surgery, radiation therapy, chemotherapy, or a combination of these treatments. The choice of treatment depends on the size, location, and stage of the cancer, as well as the patient's overall health.
Prognosis[edit | edit source]
The prognosis for ERMS depends on the stage of the disease, the size and location of the tumor, and the patient's overall health. With treatment, most children with ERMS can achieve a good quality of life.
See also[edit | edit source]
References[edit | edit source]
External links[edit | edit source]
| Embryonal rhabdomyosarcoma Resources | |
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Contributors: Prab R. Tumpati, MD
