Published online Apr 26, 2021. doi: 10.12998/wjcc.v9.i12.2923
Peer-review started: December 18, 2020
First decision: January 17, 2021
Revised: January 26, 2021
Accepted: February 22, 2021
Article in press: February 22, 2021
Published online: April 26, 2021
Processing time: 117 Days and 13.6 Hours
The incidence of breast cancer among women of reproductive age is increasing, as well as the desire for children at late childbearing age. Identifying factors that may be associated with fetal malformation and maternal and fetal prognosis has gained importance. We describe a 32-year-old woman with breast cancer who gave birth to a son with congenital bilateral cryptorchidism after treatment, with a literature review performed.
A 32-year-old woman with breast cancer who had been treated by surgery and radiotherapy experienced recurrence and underwent a second surgery, adjuvant chemotherapy, and targeted therapy. Her tumor cells were negative for estrogen receptor (ER) α, progesterone receptor (PR), and p53; positive for ERβ, human epidermal growth factor receptor-2 (HER2), epidermal growth factor receptor (EGFR), and Ki67. She had pathogenic BRCA gene mutations. She became pregnant within 2 years and delivered a boy with congenital bilateral cryptorchidism. The boy underwent bilateral orchidopexy. As of this writing, the woman and her son are both healthy.
HER2 overexpression, positivity for EGFR, Ki67, and ER, and PR negativity are associated with a poor prognosis in breast cancer. While no link has been established statistically between treatment for breast cancer and cryptorchidism in a subsequent pregnancy, this case suggests the possibility that ERβ and gene mutations may be contributing factors.
Core Tip: The number of young premenopausal women with breast cancer is increasing and they usually have a worse prognosis. Most studies focus on therapy for breast cancer. Only a few reports are published regarding fetal malformations that occur after cancer therapy. In this article, a patient got pregnant after breast cancer treatment and her son was diagnosed with congenital bilateral cryptorchidism. We conclude that there has no established link between treatments for breast cancer and cryptorchidism. Estrogen receptor β and gene mutations may be related to bilateral cryptorchidism.