History and exam
Key diagnostic factors
common
presence of risk factors
Key factors include family history of breast cancer, benign breast disease on prior biopsy, or hereditary syndromes (e.g., hereditary breast and ovarian cancer syndrome [HBOC], Li-Fraumeni syndrome, Cowden syndrome).
family history of breast cancer
Increases risk for ductal carcinoma in situ (DCIS).[32][33][34]
In a large population-based prospective cohort (UK Biobank), a positive family history of breast cancer was associated with an increased risk for DCIS among premenopausal women (hazard ratio [HR] 1.41) and postmenopausal women (HR 1.51).[32]
Increased risk of lobular carcinoma in situ (LCIS) among women with a family history of breast cancer has not been consistently demonstrated.[29][33]
Certain inherited genetic syndromes (e.g., hereditary breast and ovarian cancer syndrome [HBOC], Li-Fraumeni syndrome) increase risk for breast cancer.[35][102][37]
Other diagnostic factors
common
nipple discharge
Unilateral discharge, whether bloody or not, may indicate a benign tumour such as a papilloma, or less commonly ductal carcinoma in situ (DCIS) or invasive breast cancer.
The first symptom in males diagnosed with DCIS is generally bloody nipple discharge.[72]
uncommon
breast lump
Can be smooth or nodular.
eczema-like rash on nipple
Bleeding from, or excoriation of, the nipple are typical presenting signs of Paget's disease of the breast.
ulceration
Breast cancer that is ignored can present as an ulcerating skin lesion.
Risk factors
strong
family history of breast cancer
Increases risk for ductal carcinoma in situ (DCIS).[32][33][34]
In a large population-based prospective cohort (UK Biobank), a positive family history of breast cancer was associated with an increased risk for DCIS among premenopausal women (hazard ratio [HR] 1.41) and postmenopausal women (HR 1.51).[32]
Increased risk of LCIS among women with a family history of breast cancer has not been consistently demonstrated.[33][29]
Certain inherited genetic syndromes (e.g., hereditary breast and ovarian cancer syndrome [HBOC], Li-Fraumeni syndrome) increase risk for breast cancer.[35][36][37]
benign breast disease on prior biopsy
Increases risk for ductal carcinoma in situ up to 3.5-fold and for lobular carcinoma in situ up to 4.2-fold.[33]
hereditary breast and ovarian cancer syndrome (HBOC)
Li-Fraumeni syndrome
Li-Fraumeni syndrome is caused by mutations in the TP53 gene; it is characterised by early-onset (<40 years old) breast cancer, osteosarcoma, soft-tissue sarcomas, leukaemia, primary brain tumours, and adrenocortical carcinomas.[37] Among patients with Li-Fraumeni syndrome, up to one third of the cancers are of breast origin.[40]
Cowden syndrome
Cowden syndrome is caused by mutations in the PTEN gene.
Approximately 75% of women with Cowden syndrome have benign breast disease and 25% to 50% will develop breast cancer.[41]
hereditary diffuse gastric cancer (HDGC)
Peutz-Jeghers syndrome
Klinefelter syndrome
There is an increased risk of breast cancer in males with Klinefelter syndrome.[46]
weak
older age at menopause
Increases the risk of both ductal carcinoma in situ and lobular carcinoma in situ[33]
older age at first full-term pregnancy
Age at first birth influences risk of ductal carcinoma in situ but not so clearly lobular carcinoma in situ.[33]
nulliparity
May be associated with an increased risk of ductal carcinoma in situ but not clearly lobular carcinoma in situ.[33]
low physical activity
Lifetime physical activity is associated with an approximately 35% lower risk of in situ carcinoma of the breast compared to women with an inactive lifestyle.[47]
high vitamin A intake
High vitamin A intake may be associated with increased risk of ductal carcinoma in situ but not lobular carcinoma in situ.[48]
ataxia telangiectasia
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