Biology of high risk benign breast lesions

Author(s):  
Fred Raymond Miller
2007 ◽  
Vol 14 (4) ◽  
pp. 321-329 ◽  
Author(s):  
John V. Kiluk ◽  
Geza Acs ◽  
Susan J. Hoover

Background High-risk benign breast lesions can create confusion for both the patient and the clinician. This paper reviews the characteristics of these lesions to help direct appropriate management. Methods The authors reviewed the literature regarding high-risk breast lesions and include management guidelines that we employ at our institute. Results High-risk breast lesions offer varying degrees of increased risk for the future development of breast cancer. Chemoprevention may be used to help decrease the risks from some lesions. Conclusions The management of high-risk benign breast lesions can be confusing. Clinicians should assess the risk of future breast cancer and develop a proper screening and prevention strategy for each individual patient.


2014 ◽  
Author(s):  
Rachel L. Atkinson ◽  
Fraser Symmans ◽  
Therese B. Bevers ◽  
Wendy A. Woodward ◽  
Abenaa M. Brewster

Author(s):  
R. Santen

This chapter discusses both benign breast lesions and those that associated with an increased risk of breast cancer development, as well as the aetiology, clinical and pathologic prognosis, and hormonal treatment of breast cancers. Clinical observations in women suggest that hormones play a role in the aetiology of benign lesions. In postmenopausal women receiving oestrogens (with or without progestins) for more than 8 years, the prevalence of benign breast lesions is increased 1.7-fold; whilst the anti-oestrogen, tamoxifen, is associated with a 28 % reduction in prevalence of benign breast lesions. Cyclic and non-cyclic breast pain, nipple discharge and breast lumps are all clinical features of benign breast lesions. A practical classification, based primarily on degree of proliferation, distinguishes benign breast lesions with no associated increase in breast cancer risk from those with a small or moderate (i.e. 1.1–2.0- fold), or high risk (higher than 2.0-fold). Women considered at high risk of developing breast cancer can be treated with selective oestrogen receptor modulators (SERMS) including tamoxifen and raloxifene, which have been shown to decrease breast cancer risk by approximately 50 % when compared to placebo. The aetiology of breast cancer includes the accumulation of mutations of key genes involved in cell proliferation, DNA repair, vasculogenesis, invasion, metastasis, and apoptosis; dietary, environmental, and lifestyle factors also play a key role. The majority of risk factors for breast cancer relate to the duration or intensity of a woman’s exposure to endogenous or exogenous oestrogens; mitogenic and mutagenic effects of oestradiol probably act in concert to initiate and promote the breast cancer development. In this chapter, a variety of established and newer methods for classifying established breast cancers and predicting their prognosis and response to hormonal treatment strategies are discussed. The mechanisms (blockade of oestrogen synthesis or function) of hormonal treatments are described, as is the development of resistance to these treatments. An overview of the clinical efficacy of different hormonal treatments for breast cancer is given, as are recommended approaches to hormonal treatment of breast cancer in pre- and post-menopausal women, and in advanced disease states.


1997 ◽  
Vol 36 (08) ◽  
pp. 282-288 ◽  
Author(s):  
T. Atasever ◽  
A. Özdemir ◽  
I. Öznur ◽  
N. I. Karabacak ◽  
N. Gökçora ◽  
...  

Summary Aim: Our goal was to determine the clinical usefulness of TI-201 to identify breast cancer in patients with suspicious breast lesions on clinical examination, and/or abnormal radiologic (mammography and/or ultrasonography) findings. Methods: TI-201 scintigraphy were performed in sixty-eight patients with 70 breast abnormalities (51 palpable, 19 nonpalpable) and compared with mammography and ultrasonography (US). Early (15 min) and late (3 h) images of the breasts were obtained following the injection of 111 MBq (3 mCi) of TI-201. Visual and semiquantitative interpretation was performed. Results: Final diagnosis confirmed 52 malignant breast lesions and 18 benign conditions. TI-201 visualized 47 of 52 (90%) overall malignant lesions. Thirty-eight of 40 (95%) palpable and 9 of 12 (75%) nonpalpable breast cancers were detected by TI-201 scintigraphy. The smallest mass lesion detected by TI-201 measured 1.5x1.0 cm. Eleven breast lesions were interpreted as indeterminate by mammography and/or sonography. TI-201 scintigraphy excluded malignancy in 7 of 8 (88%) patients with benign breast lesions interpreted as indeterminate. Five of the 18 (28%) benign breast lesions showed TI-201 uptake. None of the fibroadenoma and fibrocystic changes accumulated TI-201. TI-201 scintigraphy, mammography and ultrasonography showed 90%, 92%, 85% overall sensitivity and 72%, 56%, 61% overall specificity respectively. Twenty-one of the 28 (75%) axillary nodal metastatic sites were also detected by TI-201. In malignant and benign lesions, early and late lesion/contralateral normal side (L/N) ratios were 1.58 ± 0.38 (mean ± SD) and 1.48 ± 0.32 (p >0.05), 1.87 ± 0.65 and 1.34 ± 0.20 (p<0.05) respectively. The mean early and late L/N ratios of malignant and benign groups did not show statistical difference (p>0.05). Conclusion: Overall, TI-201 scintigraphy was the most specific of the three methods and yielded favourable results in palpable breast cancers, while it showed lower sensitivity in nonpalpable cancers and axillary metastases. Combined use of TI-201 scintigraphy with mammography and US seems to be useful in difficult cases, such as dense breasts and indeterminate breast lesions.


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