With modern mammography equipment, the amount of radiation exposure is very small. Although there is no level of radiation without some risk in theory, there is no evidence of elevated risks of breast cancer from mammography is performed in a manner that is recommended. Furthermore, the benefits of early detection of far more than concern-concern in this theory.
Controversy at Area Breast Cancer Screening
There is debate about the issues screening mammography in younger women, as discussed previously. There are also issues of emotional trauma reception reports false positive mammograms (mammograms that show abnormal changes in the breast that later proved not to be cancerous). However, after evaluating women who have undergone these processes, he does not seem to be an eternal problem.
There is debate about the issues screening mammography in younger women, as discussed previously. There are also issues of emotional trauma reception reports false positive mammograms (mammograms that show abnormal changes in the breast that later proved not to be cancerous). However, after evaluating women who have undergone these processes, he does not seem to be an eternal problem.
Nor is there any suggestions that standards for screening women with high risks such as women with a family history of breast cancer in a positive or those who have inherited the genes BRCA1 or BRCA2 genes are damaged. After consulting with caution, some patients with BRCA mutations may eventually choose to run the prevention mastectomy (preventive mastectomy) to reduce the risks of breast cancer. For patients who chose surveillance (monitoring), is generally accepted that clinical breast examinations more often and perhaps, in the period, more involving imaging (ultrasound and MRI) are the minimum actions.
Benefits of Genetic Tests in the BRCA1 and BRCA2 Identify Women at Risk
In special circumstances, genetic tests can be very beneficial to both in identifying patients at high risk and reduce the level of concern for others. We also know that the presence of one of these genetic defects do not cause cancer in every patient. Cancers that occur may also behave a bit differently than tumors that are not associated with BRCA. There is some evidence that they have a better outcome.
Before genetic tests conducted, the individuals being tested should have a thorough consultation. A clear understanding of the limitations of these tests and the problems they might face should precede this testing. Patients should know the meanings of the possible outcomes, which by the way anything will come out, before testing. They also must have completed a plan for every possible outcome of the test results. Often, the best way to evaluate a potential genetic risk is to examine a brother who has been diagnosed with breast cancer. If genetic tests his brother (which should include a large number of mutations that may be) proved negative, then there is no need to carry out genetic tests on the individual concerned. However, the individual must keep a watchful eye run with breast examinations and mammograms. If the test is positive on the brothers, then the specific mutation that is the only one that needs to be examined on the individual concerned and on other family members.
In special circumstances, genetic tests can be very beneficial to both in identifying patients at high risk and reduce the level of concern for others. We also know that the presence of one of these genetic defects do not cause cancer in every patient. Cancers that occur may also behave a bit differently than tumors that are not associated with BRCA. There is some evidence that they have a better outcome.
Before genetic tests conducted, the individuals being tested should have a thorough consultation. A clear understanding of the limitations of these tests and the problems they might face should precede this testing. Patients should know the meanings of the possible outcomes, which by the way anything will come out, before testing. They also must have completed a plan for every possible outcome of the test results. Often, the best way to evaluate a potential genetic risk is to examine a brother who has been diagnosed with breast cancer. If genetic tests his brother (which should include a large number of mutations that may be) proved negative, then there is no need to carry out genetic tests on the individual concerned. However, the individual must keep a watchful eye run with breast examinations and mammograms. If the test is positive on the brothers, then the specific mutation that is the only one that needs to be examined on the individual concerned and on other family members.
