
TYPES OF RHABDOMYOSARCOMA
Types of Rhabdomyosarcoma. A rare soft tissue cancer that usually affects children and teenagers but can also strike adults is called rhabdomyosarcoma. Although it can occur anywhere in the body, rhabdomyosarcoma typically affects the muscles in the arms, legs, head, neck, and abdomen (belly). Rhabdomyosarcoma can be treated and occasionally cured by oncologists, although it might recur.
TYPES OF RHABDOMYOSARCOMA
A uncommon kind of cancer called soft tissue sarcoma is called rhabdomyosarcoma. Your skeletal muscles are where it grows. Although it can affect adults as well, rhabdomyosarcoma primarily affects children and teenagers. In the United States, 400 to 500 persons are diagnosed with rhabdomyosarcoma annually. Rhabdomyosarcomas come in a variety of forms, some of which are aggressive and more challenging to cure. In certain instances, treatment frequently results in remission of the illness.
Types

Rhabdomyosarcoma embryonal
The most prevalent kind of rhabdomyosarcoma is this one. Children are more affected than adults. The membrane that surrounds your child’s brain, eye socket, and other head and neck regions is usually where it develops.
Rhabdomyosarcoma of the alveoli
Teenagers, young adults, and older children between the ages of 20 and 35 are affected by this condition. Usually, it appears in your arms, legs, or torso. Because alveolar rhabdomyosarcoma is aggressive, it spreads swiftly after it first appears.
Rhabdomyosarcoma with pleomorphism
Adults 50 years of age and older are usually affected by this type. Although it can appear anywhere on the body, it primarily affects the legs. Additionally, it can be found in your limbs, chest, abdomen, and some areas of your head and neck.
Signs

The tumor’s location affects the symptoms. For instance, your child may experience ear pain or discharge from their ear due to a tumor in their ear. Your eye may expand or bulge out of its socket due to a tumor behind it. By tumor site, other symptoms include:
Muscle mass, lump, or swelling in the arm or leg that could be painful.
Abdomen: vomiting, constipation, or stomach pain.
Urinary tract and bladder: trouble urinating or blood in the urine (hematuria).
Nasal cavity: Symptoms of sinus infection or nosebleed (epistaxis).
Vagina: A lump or mass emerging from the vagina of your child.
Testicles: A rapidly expanding lump or mass surrounding your child’s testicles.
Causes
When immature muscle cells undergo a mutation, they develop into malignant cells that proliferate and form tumors, which is how rhabdomyosarcoma occurs. A particular kind of rhabdomyosarcoma may result from specific genetic mutations, such as one that produces the fusion gene PAX/FOX01. Li Fraumeni syndrome is more likely to develop in people with specific hereditary diseases.
Wiedemann-Beckwith syndrome.
Neurofibromatosis.
The Costello syndrome.
syndrome of the heart muscle and skin.
Treatment

The type of disease determines the treatment. Ask the cancer care team about taking part in a clinical trial if you or your kid has rhabdomyosarcoma, which is a rare condition. Oncologists typically employ the following therapies:
Surgery.
radiation treatment.
Chemotherapy.
Summary
Rhabdomyosarcoma is a very rare cancer. Experts don’t know all the reasons why it happens. If you or your child have rhabdomyosarcoma, you may feel frustrated because experts don’t know the exact cause. Your healthcare team understands those feelings. While they may not be able to explain why you or your child have rhabdomyosarcoma, they can explain the diagnosis and potential treatments, including participating in clinical trials.