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['Nceda usithumelele i-imeyile ngayo nayiphi na imibuzo / iingcebiso.']
How is breast cancer diagnosed?
Breast cancer is diagnosed through a combination of tests and procedures, which may include:
1. Clinical breast exam: A healthcare professional will examine the breasts for any lumps, changes in size or shape, or other abnormalities.
2. Mammogram: An x-ray of the breast that can detect abnormalities even before they can be felt.
3. Ultrasound: A test that uses sound waves to create an image of the breast tissue, which can help determine if a lump is solid or filled with fluid.
4. MRI: A magnetic resonance imaging (MRI) scan uses a magnetic field and radio waves to create detailed images of the breast tissue.
5. Biopsy: A small sample of breast tissue is removed and examined under a microscope to determine if cancer cells are present.
6. Blood tests: Certain blood tests, such as a complete blood count or tumor markers, may be done to help determine the stage of the cancer or to monitor treatment.
7. Genetic testing: If there is a family history of breast cancer, genetic testing may be done to determine if there is an inherited gene mutation that increases the risk of developing breast cancer.
8. Bone scan, CT scan, or PET scan: These imaging tests may be done to determine if the cancer has spread to other parts of the body.
Once a diagnosis of breast cancer is made, further tests may be done to determine the stage and grade of the cancer, which helps guide treatment decisions.
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Please note the neural net that generates answers to the questions, is specially inaccurate when it comes to numeric content. For example, the number of people diagnosed with a specific disease.
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