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      Breast cancer arising within fibroadenoma: collective analysis of case reports in the literature and hints on treatment policy

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          Abstract

          Background

          Breast cancer arising within a fibroadenoma (BcaFad) is rare; the rate varies from 0.002% to 0.125% in fibroadenoma specimens. Owing to its rarity, the clinicopathologic feature and treatment principle of BcaFad is still not clear. Therefore, the aim of this study was to perform a collective analysis of case reports in the literature to identify the characteristics and optimal treatment for BcaFad.

          Methods

          We analyzed an aggregated sample of 30 patients with BcaFad from case reports in the literature ( n =24 cases) and our present study ( n =6 cases). We collected and analyzed the clinicopathologic features and prognoses of patients with BcaFad, as well as treatments they received.

          Results

          The patients’ mean age at diagnosis was 46.9 years. Twenty BcaFad patients (66.7%) received breast-conserving surgery (BCS), and nine other patients (30.0%) were treated with mastectomy. The rate of lymph node metastasis in BcaFad patients was 23.8%. The breakdown of the histological types of BcaFad was invasive ductal carcinoma (53.3%), followed by ductal carcinoma in situ (23.3%), lobular carcinoma in situ (16.7%) and invasive lobular carcinoma (13.3%). More than half of patients with positive hormone receptor status received hormone therapy. Most BcaFad patients with lymph node metastases received chemotherapy, and 20.0% of BcaFad patients treated with BCS received further radiotherapy. Only one patient had recurrence after surgery, and another had lung metastasis when diagnosed with BcaFad.

          Conclusions

          Most BcaFad patients could be managed by BCS. Adjuvant radiotherapy could be performed, but was not mandatory. Chemotherapy should be considered as a treatment option in the presence of lymph node metastasis.

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          Most cited references50

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          Twenty-Year Follow-up of a Randomized Trial Comparing Total Mastectomy, Lumpectomy, and Lumpectomy plus Irradiation for the Treatment of Invasive Breast Cancer

          New England Journal of Medicine, 347(16), 1233-1241
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            Infiltrating lobular carcinoma of the breast. Clinicopathologic analysis of 975 cases with reference to data on conservative therapy and metastatic patterns.

            The clinicopathologic features of infiltrating lobular carcinoma (ILC), which represents 5% to 15% of all breast cancers, are still controversial. In particular, the high frequency of multicentric lesions has led to questioning of the effectiveness of conservative treatment for this type of cancer. By studying a large number of cases, we aimed to compare the clinicopathological features of ILC with those of nonlobular infiltrating carcinoma (NLIC) and to assess the advisability of conservative therapy in the management of ILC. The population analyzed included 726 cases of ILC, 249 cases of mixed ILC/invasive ductal carcinoma (ILC/IDC), and 10,061 cases of NLIC. The age of patients, TNM status, estrogen- and progesterone-receptor status (ER, PR), and histologic grades of the 3 groups were compared. The follow-up was carried out on a subgroup of 5846 cases. At diagnosis, ILC tumors were found to be larger on average and were detected in patients older than those with NLIC, but the degree of lymph node involvement was lower in patients with ILC than in NLIC. In ILC, tumors are more frequently grade I and ER-positive than in NLIC. Multicentric lesions were not significantly more frequent in ILC than in NLIC. The overall survival, locoregional control, disease free interval, and metastatic spread rates were not different among the three groups neither by univariate nor multivariate analysis, but the pattern of metastatic dissemination was different. In 480 cases of ILC considered for conservation therapy, the local recurrence and overall survival rates were similar to those observed for IDC. Our analysis specifies the clinicopathological features of ILC and confirms that conservation therapy may be an appropriate treatment for this type of cancer.
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              Long-term risk of breast cancer in women with fibroadenoma.

              Fibroadenomas are benign breast tumors that are commonly diagnosed in young women and are associated with a slight increase in the risk of breast cancer. These lesions vary considerably in their histologic characteristics. We assessed the correlation between the histologic features of fibroadenomas and the risk of subsequent breast cancer. We conducted a retrospective cohort study of a consecutive series of patients with fibroadenoma diagnosed between 1950 and 1968. Follow-up data were obtained for 1835 patients (90 percent of those eligible). Fibroadenomas with cysts, sclerosing adenosis, epithelial calcifications, or papillary apocrine changes were classified as complex. The rate of subsequent breast cancer among the patients was compared with the rates in two control groups, women listed in the Connecticut Tumor Registry and women chosen from among the patients' sisters-in-law. The risk of invasive breast cancer was 2.17 times higher among the patients with fibroadenoma than among the controls (95 percent confidence interval, 1.5 to 3.2). The relative risk increased to 3.10 among patients with complex fibroadenomas (95 percent confidence interval, 1.9 to 5.1) and remained elevated for decades after diagnosis. Patients with benign proliferative disease in the parenchyma adjacent to the fibroadenoma had a relative risk of 3.88 (95 percent confidence interval, 2.1 to 7.3). Patients with a family history of breast cancer in whom complex fibroadenoma was diagnosed had a relative risk of 3.72, as compared with controls with a family history (95 percent confidence interval, 1.4 to 10). Two thirds of the patients had noncomplex fibroadenomas and no family history of breast cancer and did not have an increased risk. Fibroadenoma is a long-term risk factor for breast cancer. The risk is increased in women with complex fibroadenomas, proliferative disease, or a family history of breast cancer.
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                Author and article information

                Contributors
                taichung1031@hotmail.com
                1886@cch.org.tw
                132540@cch.org.tw
                ylkuo@mail.ncku.edu.tw
                lmtseng@vghtpe.gov.tw
                115045@cch.org.tw
                40225@cch.org.tw
                143809@cch.org.tw
                Journal
                World J Surg Oncol
                World J Surg Oncol
                World Journal of Surgical Oncology
                BioMed Central (London )
                1477-7819
                10 November 2014
                2014
                : 12
                : 1
                : 335
                Affiliations
                [ ]Endoscopic and Oncoplastic Breast Surgery Center, Comprehensive Breast Cancer Center, Changhua Christian Hospital, 135 Nanhsiao Street, Changhua City, Changhua County 500 Taiwan
                [ ]Division of General Surgery, Changhua Christian Hospital, 135 Nanhsiao Street, Changhua City, Changhua County 500 Taiwan
                [ ]Department of Surgery, Comprehensive Breast Cancer Center, Changhua Christian Hospital, 135 Nanhsiao Street, Changhua City, Changhua County 500 Taiwan
                [ ]Department of Surgery, Sinying Hospital, Ministry of Health and Welfare, 73 Xinyi Street, Xinying Dist, Tainan City, 730 Taiwan
                [ ]Department of Surgical Pathology, Changhua Christian Hospital, 135 Nanhsiao Street, Changhua City, Changhua County 500 Taiwan
                [ ]School of Medicine, Chung Shan Medical University, Taichung, No. 110, Sec. 1, Jianguo N. Rd, Taichung City, 40201 Taiwan
                [ ]Department of Medical Technology, Jen-Teh Junior College of Medicine, Nursing and Management, No 79-9, Sha-Luen Hu, Xi-Zhou Li, Hou-Loung Town, Miaoli County, Taiwan
                [ ]Division of General Surgery, Department of Surgery, National Cheng-Kung University Hospital, Tainan and Dou-Liou branches, No.138, Sheng Li Road, Tainan 704, Taiwan and No.345, Zhuangjing Rd, Douliu City, Yunlin County 64043 Taiwan
                [ ]Division of Plastic and Reconstructive Surgery, Department of Surgery, National Cheng-Kung University Hospital, Tainan and Dou-Liou branches, No.138, Sheng Li Road, Tainan 704, Taiwan and No.345, Zhuangjing Rd, Douliu City, Yunlin County 64043 Taiwan
                [ ]Division of General Surgery, Department of Surgery, Taipei Veterans General Hospital, No.201, Sec. 2, Shipai Rd., Beitou District, Taipei City, 11217 Taiwan
                [ ]School of Medicine, National Yang Ming University, Taipei, No.155, Sec.2, Linong Street, Taipei, 112 Taiwan
                Article
                1863
                10.1186/1477-7819-12-335
                4289362
                25382741
                70b2d09f-4239-4a92-87f4-10895102b40b
                © Wu et al.; licensee BioMed Central Ltd. 2014

                This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 3 April 2014
                : 25 September 2014
                Categories
                Research
                Custom metadata
                © The Author(s) 2014

                Surgery
                breast cancer,fibroadenoma,hormone therapy,radiotherapy
                Surgery
                breast cancer, fibroadenoma, hormone therapy, radiotherapy

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