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Abstract

One of the most significant risk factors for developing early onset breast cancer is the presence of a BRCA1/2 mutation. The presence of a BRCA1/2 mutation confers a 40–90 % lifetime risk of developing breast cancer and up to a 60 % lifetime risk of developing ovarian cancer. BRCA1/2 plays an important role on the causal pathway for developing breast cancer and has a significant impact on the biological and clinical characteristics of BRCA1/2-associated breast cancer. The presence of a BRCA1/2 mutation has far-reaching impact on the full spectrum of reproductive issues, including the impact of risk-reducing salpingo-oophorectomy both on fertility and premature menopause. The presence of a BRCA1/2 mutation compounds the already complex and multifactorial challenges that exist when managing a young woman with breast cancer – the challenges range from medical (oncological, gynecological, surgical) to psychosocial and ethical; thus, a multidisciplinary approach is mandatory.

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Correspondence to Shani Paluch-Shimon .

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Paluch-Shimon, S., Meirow, D., Hyman, J. (2015). Reproductive Issues in BRCA Mutation Carriers. In: Biglia, N., Peccatori, F. (eds) Breast Cancer, Fertility Preservation and Reproduction. Springer, Cham. https://doi.org/10.1007/978-3-319-17278-1_7

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