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Neuro-Oncologic Complications of Breast Cancer

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Cancer Neurology in Clinical Practice
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Abstract

Breast cancer arises from the epithelial cells that line the ducts and lobules of the mammary gland. Its incidence has increased gradually (1–2%/yr for the last three decades), but recently the incidence has leveled off and mortality has even decreased slightly. At present, about 1 out of every 10 females in the United States and Western Europe will develop breast cancer. The risk of breast cancer rises steadily from about the age of 25, with some slowing of increase after menopause. Obviously, hormones are important promoters of the disease. Length of menstrual life and the fraction until first pregnancy are established risk factors of breast cancer. Other factors include exposure to radiotherapy (RT) before the age of 30, and to some extent long-term postmenopausal estrogen replacement. A family history of breast cancer is the most important risk factor (1). About 5-10% of all breast cancers occur in high-risk families, including families with the Li-Fraumeni syndrome (mutation in p53) and families with mutation in the tumor suppressor gene BRCA 1 or BRCA 2 (lifetime risk of breast cancer up to 85%). In sporadic breast cancer p53 mutation is found in 40% of the patients and overexpression of the oncogene erb B2 (HER-2/neu) in a quarter of the patients (2).

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Boogerd, W. (2003). Neuro-Oncologic Complications of Breast Cancer. In: Schiff, D., Wen, P.Y. (eds) Cancer Neurology in Clinical Practice. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-317-0_21

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  • DOI: https://doi.org/10.1007/978-1-59259-317-0_21

  • Publisher Name: Humana Press, Totowa, NJ

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