Chordoma is a rare type of cancer that develops in the bones of the skull and spine. It originates from remnants of the notochord, a structure that plays a key role in the development of the spinal column. Chordomas are slow-growing tumors that can cause symptoms such as headaches, back pain, and difficulty walking.
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This article is for information only and not for treatment.
If you have any medical problem, consult a good doctor.
If you follow these medical advices, do so at your own risk.
Currently, there is no known way to prevent chordoma, as the exact cause of the condition is not fully understood. However, some factors that may increase the risk of developing chordoma include:
Genetics: There may be a genetic component to chordoma, as the condition can sometimes run in families.
Age: Chordoma is more commonly diagnosed in adults over the age of 40.
Gender: Chordoma is slightly more common in men than in women.
Exposure to radiation: Previous exposure to radiation may increase the risk of developing chordoma.
While it may not be possible to prevent chordoma, early detection and treatment can improve outcomes for individuals with the condition. Treatment options may include surgery, radiation therapy, and chemotherapy, depending on the size and location of the tumor and other factors. It's important for individuals with symptoms such as headaches, back pain, and difficulty walking to speak with a healthcare professional, who can perform tests to determine the cause of the symptoms and develop an appropriate treatment plan.
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