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Soft Tissue Sarcoma Symptoms - Oren Zarif - Soft Tissue Sarcoma


There are several types of Soft Tissue Sarcomas, but some are more common than others. Rhabdomyosarcoma, for example, is a very common form of the disease. It develops in striated muscle tissue that attaches to the skeleton through tendons. Voluntary muscles are those that can be controlled by conscious thought. Involuntary muscles are those that are not controlled by conscious thought, such as the heart and intestines.

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The symptoms of soft tissue sarcomas vary, depending on where it has spread. The tumor may be painless or have no apparent symptoms until it grows large enough to cause symptoms. The lump may press on an organ, nerve, or muscle. Although most soft tissue sarcomas are painless, they can cause swelling, which may be painful or innocuous. If you notice any of these symptoms, you should seek medical attention.

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Some people may notice a growing mass in a leg or arm. A mass can also cause a fullness sensation in that limb. The mass itself is painless, but pressing on a nearby nerve may cause numbness or tingling sensations. Further evaluation of soft tissue sarcoma symptoms is important. However, this can also be caused by other, less serious ailments. If you suspect you have a lump, see a doctor right away.

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A biopsy is an important part of diagnosing soft tissue sarcoma in adults. A biopsy can be performed to remove part of the lump or examine it microscopically. Alternatively, the tumor may be removed in its entirety. Most doctors recommend an incisional biopsy before performing surgery, but this is not always necessary. The biopsy also helps determine whether the disease has spread elsewhere in the body. There are many treatments for the disease, but the only surefire way to know is to consult with a physician.

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Early stages of the disease do not typically produce any soft tissue sarcoma symptoms. However, the signs and symptoms of soft tissue sarcoma will appear as the tumour presses on certain body parts. It is important to note that many people experience similar symptoms, and it is possible that soft tissue sarcoma could be mistaken for something else. If you develop any lump in an area other than the one you're concerned about, it is a good idea to see a doctor.

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As with any type of cancer, early diagnosis is essential for successful treatment. Early diagnosis can significantly improve your chances of survival. If you suspect that you have a tumor, it's best to consult with a specialist immediately. The sooner you detect it, the better chance it has of being detected and treated. It's important to know that half of all patients survive for five years or more. This is the reason why diagnosis is so critical.

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Certain diseases can increase your risk of developing a soft tissue sarcoma. These include radiation therapy, chemicals and lymphedema. Although these factors are rare, some people have a genetic predisposition to this condition. You should consult a doctor as soon as you suspect a diagnosis of soft tissue sarcoma. And remember that cancer is not always fatal. Just because it's rare doesn't mean you can't have it.

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Often, soft tissue sarcoma symptoms are not readily apparent. Most cancer patients don't exhibit symptoms during its early stages. Fortunately, half of soft-tissue sarcomas are diagnosed at an early stage before it spreads. Some tumors may cause discomfort or blockage in the abdomen, and in rare cases they can even grow large enough to be felt. While there are no definitive signs that you have soft tissue sarcoma, the symptoms can help you decide whether to undergo a diagnosis.

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Most soft tissue sarcomas are painless and appear in the body as a lump. They can be in any part of the body but are most common in the thigh, arm, or pelvis. If detected early, the cancer may be curable and treatment is generally surgical. In certain cases, chemotherapy may also be prescribed. It may be difficult to detect, but if you notice any signs, it is time to seek medical attention.

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Treatment for soft tissue sarcomas is aggressive and can affect nearly any part of the body. The most common site for angiosarcoma is the skin of the head and neck, but it can also be found in the lower extremities, the area behind the abdominal cavity, and the chest. Rarely, cutaneous angiosarcoma can be a late effect of radiation treatment for breast cancer.

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