Breast Cancer : The Most Common Cancer Essay

There are no symptoms at the early stages of breast cancer which makes early detection even more difficult. When tumors become large there is an obvious breast mass which is mostly not painful. Symptoms of breast cancer include breast thickening, skin irritation, tenderness, swelling, breast scales, distortion, redness tenderness, nipple retraction and ulceration, There may also be abnormal discharge.

We have all seen the pink ribbons. They have become a national, if not international symbol for breast cancer support and awareness. Breast cancer knows neither racial boundaries nor age restrictions. Females of all ages and ethnicities can develop breast cancer and it is the leading most common cancer among women. Calling attention to this often fatal disease is important by supporting its victims, families and friends of victims, as well as raising funds for breast cancer research. Though males are not immune from developing a breast cancer, for the purposes of this paper, this paper will be limited to information relating breast cancer in females.

According to the United States Breast Cancer Statistics (2016), in 2016 there will be an estimated 246,660 newly diagnosed cases of invasive breast cancer and 61,000 of non-invasive breast cancer among women. For this reason, when studying breast cancer based on a large-scale impact, it not only affects the patient themselves but, as well as their families and communities nationwide. Furthermore, many contributing factors lead to this being such a public health issue. Conclusively, there are specific programs, services, and policies that help to assist the contributing factors of such a public health threat. Nevertheless, breast cancer is still an increasing concern in society, and much-needed research is required to be able to detect and treat this disease.

Women who are at the greatest risk are over the age over the age of fifty years of age. Patients with a family history of cancer, especially in their first degree relatives, may have inherited mutations of BRCA1 and/or BRCA2. BRCA1 and BRCA2 are genetic mutations that put patients are risk for cancer. Patients that have a history of breast cancer are five times more likely of developing cancer in the opposite breast. Patients with dense breast are at risk for developing breast cancer due to the fact dense breast contains more glandular and connective tissue. Patients who are exposed to high doses of ionizing radiation to the thorax, early menarche, tobacco use, nulliparity, late menopause, and first child birth after thirty years of age put the patient at risk for breast cancer (Ignatavicius, 2013, p.

Despite significant advances in research, Breast Cancer is still the most common cancer, affecting both men and especially women. In the US, 232, 670 new cases of invasive breast cancer were expected to be diagnosed along 62,570 new cases of non-invasive breast cancer in women and about 2,360 new cases of invasive breast cancer were expected to be diagnosed in men in just 2014 .

Hereditary breast and ovarian cancer is mostly due to a mutation in the Breast cancer susceptibility gene 1(BRCA1) and breast cancer susceptibility gene 2 (BRCA 2) genes and is the most common cause of both forms of breast and ovarian cancers due to hereditary (Weitzel, Blazer, MacDonald, Culver, & Offit, 2011). Although the overall prevalence of the BRCA 1/2 genes is estimated 1 in 400 to 1 in 800 with a higher occurrence in the Ashkenazi Jewish population which is 1 in 40 that have the BRCA genes. According to Weitzel, Blazer, MacDonald, Culver, & Offit (2011), the likelihood of having the BRCA1 or BRCA2 mutation is dependent on one’s personal and/or family history of cancer and can be assessed by using several mutation probability models. After a BRCA1 or BRCA2 gene has been identified in the family, testing of all of at-risk relatives can identify those family members who may also have the BRCA gene and therefore will need to have an increased in following and early intervention when a cancer is diagnosed. There are several options that a person who has been diagnosed with having

High-risk families include those whose members carry a mutation in the BRCA2 gene. The mutated BRCA2 gene is inherited in an autosomal dominant pattern. A child needs to inherit just one copy of the mutated gene to have an increased cancer risk. Children who have a parent with a BRCA2

Breast cancer is the most common cancer that affects women in the United States. There are at least two majors genes (BRCA1 and BRCA2) that when they mutate can cause breast cancer. These genes can be passed from parent to child, increasing the risk of developing cancer in those child that have parent carrying these genes. BRCA1 and BRCA2 genes are located on chromosome 17 and chromosome 13 respectively. There is a 90% chance of developing breast cancer for a woman that has these mutated genes. In contrast, men carrying BRCA1 have no risk to develop breast cancer, but those carrying BRCA2 genes have high risk. It is important to note that mutations in these genes can be passed on to children by either parent. A man with a mutation is just

     Breast cancer, a very painful disease emotionally and physically for women, can also be detected with genetic testing. The majority of cases of breast cancer are not the result of known inherited mutations, but rather from two breast cancer susceptibility genes: BRCA1 and BRCA2. Although the two genes are similar, BRCA1 mutations lead to estrogen receptor negative

My mother, Bonita, was diagnosed with breast cancer at age 45. She first discovered the lump herself and proceeded to take it to a professional to get it checked out. There is no evidence in her immediate family to say that this is hereditary, but a combination of a few factors increased her risk of getting breast cancer. My mother was overweight, has had an early menstruation (before age 12), lived a sedentary lifestyle, and at the time she didn’t have a well-balanced diet. Along with those factors, her doctors pointed out that her risk could have been increased by her use of an oral contraceptive.

List the factors in the patient’s history that increase the risk of developing breast cancer.

Breast Cancer affects one in eight of American women, and is the second most common cause of cancer death in America. I chose to write my term paper on breast cancer because it is a disease that has effected some members of my family. Due to this possibly inherited condition, I felt that researching the topic would help me learn ways to prevent the disease and educate myself to perform self-exams that may result in early detection.

Breast cancer is the most common type of cancer in women, it accounts for one of every three diagnoses in the United States. Breast cancers are malignancies, life threatening tumors that develops in one or both breasts.

Meanwhile, in addition to the male's occupation, radiation exposure and age can lead to breast cancer developments ( National Cancer Institute, 2007). When these risk factors are revealed in a diagnoses of breast cancer, men have more advanced cancerous growths than women (Giordano, 2004). So men may think, how do I get breast cancer? Is it inherited?

Breast cancer is the second leading cancer killer among women, after lung cancer (Breast Cancer , 2014). Cancer is a word that puts fear in many people, especially if they have family members who have either died or survived the disease. No one wants to hear that he or she has been diagnosed with any disease, especially cancer. Many women do not take breast cancer serious until they are diagnosed. Sadly, once diagnosed with this epidemic, a person’s life is altered forever. Breast cancer does not discriminate and can happen to anyone at any age. To prevent this disease, one must take the necessary precautions to lower the risk factors. In fact, there are several local and national events to remind people of breast cancer’s existence. Many