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Consensus Statement

Clinical practice guideline for breast fibroadenoma: Chinese Society of Breast Surgery (CSBrS) practice guideline 2021

Peng, Yuan1; Xie, Fei1; Zhao, Yi2; Wang, Shu1

Editor(s): Ji, Yuan-Yuan

; Chinese Society of Breast Surgery

Author Information
doi: 10.1097/CM9.0000000000001462
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Breast fibroadenoma is the most common benign tumor of the breast in women, and can occur at all ages. However, these tumors are more commonly seen in women aged 15 to 35 years.[1] Most fibroadenomas often undergo self-limited growth and usually stabilize after several years. The clinical diagnosis is mainly based on clinical palpation and ultrasonographic examination, while the golden standard diagnosis is pathological examination. To standardize the clinical diagnosis and treatment of breast fibroadenoma, the Chinese Society of Breast Surgery (CSBrS) conducted a literature review of experts’ opinions, and determined the key clinical questions for the clinical practice guideline of breast fibroadenoma. The group evaluated the relevant evidences using the grading of recommendations assessment, development, and evaluation system, and developed the clinical practice guideline for breast fibroadenoma: CSBrS practice guideline 2021, with the aim of providing clinical practice guidance to breast surgeons in China.

Level of Evidence and Recommendation Strength

Level of evidence standard[2]

Recommendation strength standard[2]

Recommendation strength review committee

There were 79 voting committee members for these guidelines: 67 from breast surgery departments (84.8%), three from medical oncology departments (3.8%), four from medical imaging departments (5.1%), two from a pathology department (2.5%), one from radiology department (1.3%), and two epidemiologists (2.5%).

Target Audience

Clinicians specializing in breast diseases in China.

Recommendations

Recommendation 1: Diagnosis of fibroadenoma 

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Diagnosis of fibroadenoma Level of evidence Recommendation strength
1.1 Clinical palpation[3] II A
1.2 Ultrasonography[4–9] I A
1.3 Pathology[3,10–12] I A

Recommendation 2: Surgical treatment 

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Surgical treatment Level of evidence Recommendation strength
2.1 Indications
 2.1.1 Rapid growth[13] II A
 2.1.2 Large size (>3 cm)[13] II A
 2.1.3 BI-RADS category increased[3,13] I A
 2.1.3 Core needle biopsy suggested with atypical hyperplasia or suspected phyllodes tumor[13] I A
2.2 Surgical options
 2.2.1 Open excision[3] I A
 2.2.2 Ultrasound-guided VABB[3,14–16] II A
For fibroadenomas where VABB is planned, please refer to the Clinical Practice Guidelines for Ultrasound-guided Vacuum-assisted Breast Biopsy for details. BI-RADS: Breast Imaging Reporting and Data System; VABB: Vacuum-assisted breast biopsy.

Recommendation 3: Non-surgical treatment 

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Non-surgical treatment Level of evidence Recommendation strength
3.1 Indications
 3.1.1 BI-RADS category 3[3,17] I A
 3.1.2 Sonographically-typical fibroadenomas in a young patient[8,9,18] II A
3.2 Follow-up interval
 3.2.1 Every 6 months[17] I A
3.3 Follow-up method
 3.3.1 Clinical palpation combined with ultrasonography[3,17] I A
 3.3.2 Annual mammography starting at age 40 years[17] I A
BI-RADS: Breast Imaging Reporting and Data System.

Discussion

Fibroadenoma is the most common benign breast tumor in women. Most fibroadenomas form as a single tumor, and in approximately 15% of patients, multiple tumors are present.[19] Clinical palpation reveals mostly oval, rubber-like masses with clear boundaries and good mobility. However approximately 25% to 35% of affected patients have negative palpation findings.[20–22]

The clinical diagnosis of fibroadenoma is mainly based on palpation and imaging examinations, namely ultrasonography, mammography, and magnetic resonance imaging (MRI). The reported that the accuracy of breast ultrasonography in the diagnosis of fibroadenoma is 78.8% to 99.5%.[4–9] The specificity of mammography for diagnosing of fibroadenoma is 83.9%, which is lower than that for ultrasonography (88.2%),[23] but mammography has outstanding advantages for differentiating malignant from benign calcification. Breast enhanced MRI can further improve the diagnostic accuracy rates for fibroadenomas.[24] According to the characteristics of the Chinese female mammary gland, the guidelines panel recommends ultrasonography examination first. In patients aged ≥40 years with a mass with suspected microcalcification or not excluded as malignant, mammography is recommended. Considering the economic cost, enhanced MRI is not recommended as a conventional imaging method for diagnosing fibroadenoma. For multiple lesions and an unclear diagnosis after ultrasonography and mammography, MRI can be selected as appropriate.

Pathological examination is the golden standard for diagnosing fibroadenoma. Fine needle aspiration, core needle biopsy, vacuum-assisted breast biopsy, and excision biopsy are all available methods. The reported accuracy of fine needle aspiration cytology for diagnosing fibroadenoma ranges from 36.3% to 91.7%,[25–28] and the diagnostic accuracy of core needle biopsy can be as high as 93.4% to 98.3%,[10,11] with minimal tissue damage. Therefore, the guidelines panel recommends core needle biopsy as the first choice for the pathological diagnosis of fibroadenoma.

The incidence of malignancy in fibroadenoma is very low, therefore, regular follow-up after core needle biopsy diagnosed as fibroadenoma is safe. For Breast Imaging Reporting and Data System (BI-RADS) category 3 fibroadenoma, the guidelines panel recommends clinical palpation combined with ultrasonography examination every 6 months. For patients with stable lesions followed up regularly for 2 years, the follow-up interval may be extended to once every 12 months. For patients ≥40 years old, mammography is recommended according to the breast cancer screening guidelines and the standards of the American College of Radiology.[17] It is safe not to biopsy of typical fibroadenomas in young women when the clinical and sonographic presentations meet strict criteria. This is because, in these patients, ultrasonography and pathology have good concordance rates, and a missed diagnosis of malignant disease is rare.[8,9,18]

Open excision is the most effective surgical intervention for fibroadenoma, especially for large tumors. Ultrasound-guided vacuum-assisted breast biopsy is also safe for fibroadenomas of appropriate size and location, especially for patients with high aesthetic requirements.[3,14–16] However, with lager tumors, the possibility of residual lesions is greater; therefore, ultrasound-guided vacuum-assisted breast biopsy is generally not recommended for tumors larger than 3 cm. Phyllodes tumors are indistinguishable from fibroadenoma with ultrasonography and mammography. Considering that pre-operative biopsy is also insufficient to distinguish phyllodes tumor from fibroadenoma, and there is the possibility of underestimation,[29–31] referring to the NCCN clinical practice guidelines in oncology for breast cancer, about phyllodes tumor, the CSBrS guidelines panel recommends that tumors larger than 3 cm are an indication for surgical treatment.[13] Rapid growth is also an indication for surgical treatment. The criteria for rapid growth are: (1) volume growth rate ≥16% per month for patients younger than 50 years, (2) volume growth ≥13% per month for patients ≥50 years, and (3) mean change in dimension over a 6-month interval of >20%.[32] In addition, an increased BI-RADS classification grade during the follow-up and core needle biopsy suggesting with atypical hyperplasia or suspected phyllodes tumor are also indications for surgical treatment.

List of Compiling Committee Members (in alphabetical order by surname)

Zhong-Wei Cao, De-Dian Chen, Yuan-Jia Cheng, Xue-Ning Duan, Zhi-Min Fan, Pei-Fen Fu, Bao-Liangguo, Jian Huang, Jun Jiang, Hong-Chuan Jiang, Feng Jin, Hua Kang, Rui Ling, Jin-Ping Liu, Ke Liu, Li-Yuan Liu, Miao Liu, Qian Liu, Yin-Hua Liu, Yun-Jiang Liu, Zhen-Zhen Liu, Da-Hua Mao, Jiang-Hua Ou, Yuan Peng, Xiang Qu, Guo-Sheng Ren, Ai-Lin Song, Er-Wei Song, Li-Li Tang, Xing-Song Tian, Chao-Bin Wang, Chuan Wang, Fei Wang, Jiang-Dong Wang, Shu Wang, Shui Wang, Xiang Wang, Jiong Wu, Fei Xie, Ling Xin, Zhi-Gang Yu, Jiang-Guo Zhang, Jin Zhang, Jing-Hua Zhang, Wei Zhu, Ang Zheng, Qiang Zou

Conflicts of interest

The expert committee for these guidelines declares no conflict of interest. These guidelines are a reference for breast disease specialists in clinical practice. However, the guidelines are not to be used as the basis for medical evaluation, and do not play an arbitrating role in the handling of any medical disputes. The guidelines are not a reference for patients or non-breast specialists. The CSBrS assumes no responsibility for results involving the inappropriate application of these guidelines, and reserves the right to interpret and revise the guidelines.

References

1. EI-Wakeel H, Umpleby HC. Systematic review of fibroadenoma as a risk factor for breast cancer. Breast 2003; 12:302–307. doi: 10.1016/s0960-9776(03)00123-1.
2. Ye JM, Guo BL, Liu Q, Ma F, Liu HJ, Wu Q, et al. Clinical Practice Guidelines for sentinel lymph node biopsy in patients with early-stage breast cancer: Chinese Society of Breast Surgery (CSBrS) practice guidelines 2021. Chin Med J 2021; 134:886–894. doi: 10.1097/CM9.0000000000001410.
3. National Center for Women's Health, Chinese Preventive Medicine Association. Consensus on diagnosis and treatment of breast fibroadenoma (in Chinese). Chin J Prac Surg 2016; 36:752–754. doi: 10.7504/CJPS.ISSN1005-2008.2016.07.11.
4. Stavros AT, Thickman D, Rapp CL, Dennis MA, Parker SH, Sisney GA. Solid breast nodules: use of sonography to distinguish between benign and malignant lesions. Radiology 1995; 196:123–134. doi: 10.1148/radiology.196.1.7784555.
5. Skaane P, Engedal K. Analysis of sonographic features in the differentiation of fibroadenoma and invasive ductal carcinoma. AJR Am J Roentgenol 1998; 170:109–114. doi: 10.2214/ajr.170.1.9423610.
6. Cole-Beuglet C, Soriano RZ, Kurtz AB, Goldberg BB. Fibroadenoma of the breast sonomammography correlated with pathology in 122 patients. AJR Am J Roentgenol 1983; 140:369–375. doi: 10.2214/ajr.140.2.369.
7. Ban K, Tsunoda H, Suzuki S, Takaki R, Sasaki K, Nakagawa M. Verification of recall criteria for masses detected on ultrasound breast cancer screening. J Med Ultrason (2001) 2018; 45:65–73. doi: 10.1007/s10396-017-0778-5.
8. Taylor K, Lowes S, Stanley E, Hamilton P, Redman A, Leaver A, et al. Evidence for avoiding the biopsy of typical fibroadenomas in women aged 25-29 years. Clin Radiol 2019; 74:676–681. doi: 10.1016/j.crad.2019.02.019.
9. Cant PJ, Madden MV, Close PM, Learmonth GM, Hacking EA, Dent DM. Case for conservative management of selected fibro-adenomas of the breast. Br J Surg 1987; 74:857–859. doi: 10.1002/bjs.1800740936.
10. Lee S, Mercado CL, Cangiarella JF, Chhor CM. Frequency and outcomes of biopsy-proven fibroadenomas recommended for surgical excision. Clin Imaging 2018; 50:31–36. doi: 10.1016/j.clinimag.2017.12.008.
11. Hubbard JL, Cagle K, Davis JW, Kaups KL, Kodama M. Criteria for excision of suspected fibroadenomas of the breast. Am J Surg 2015; 209:297–301. doi: 10.1016/j.amjsurg.2013.12.037.
12. Neville G, Neill CO, Murphy R, Corrigan M, Redmond PH, Feeley L, et al. Is excision biopsy of fibroadenomas based solely on size criteria warranted? Breast J 2018; 24:981–985. doi: 10.1111/tbj.13069.
    13. National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology version 6, 2020: Breast. NCCN Clinical Practice Guidelines in Oncology. Available from: https://www.nccn.org. Accessed October 12, 2020.
    14. Fine RE, Whitworth PW, Kim JA, Harness JK, Boyd BA, Burak WE Jr. Low-risk palpable breast masses removed using a vacuum-assisted hand-held device. Am J Surg 2003; 186:362–367. doi: 10.1016/s0002-9610 (03)00263-0.
    15. Grady I, Gorsuch H, Wilburn-Bailey S. Long-term outcome of benign fibroadenomas treated by ultrasound-guided percutaneous excision. Breast J 2008; 14:275–278. doi: 10.1111/j.1524-4741.2008.00574.x.
    16. Park HL, Kim KY, Park JS, Shin JE, Kim HR, Yang B, et al. Clinicopathological analysis of ultrasound-guided vacuum-assisted breast biopsy for the diagnosis and treatment of breast disease. Anticancer Res 2018; 38:2455–2462. doi: 10.21873/anticanres.12499.
    17. Harvey JA, Mahoney MC, Newell MS, Bailey L, Barke LD, D’Orsi C, et al. ACR appropriateness criteria palpable breast masses. J Am Coll Radiol 2016; 13:e31–e42. doi: 10.1016/j.jacr.2016.09.022.
    18. Smith GE, Burrows P. Ultrasound diagnosis of fibroadenoma - is biopsy always necessary? Clin Radiol 2008; 63:511–515. doi: 10.1016/j.crad.2007.10.015.
    19. Ferrara A. Benign breast disease. Radiol Technol 2011; 82:447M–462M.
    20. Wilkinson S, Anderson TJ, Rifkind E, Chetty U, Forrest AP. Fibroadenoma of the breast: a follow-up of conservative management. Br J Surg 1989; 76:390–391. doi: 10.1002/bjs.1800760424.
    21. Pruthi S. Detection and evaluation of a palpable breast mass. Mayo Clinic proceedings. Mayo Clin Proc 2001; 76:641–647. doi: 10.4065/76.6.641.
    22. Mühlberger G, Lauth G. Value of palpation findings in breast examination (in German). Geburtshilfe Frauenheilkd 1993; 53:772–775. doi: 10.1055/s-2007-1023724.
    23. Zimmermann N, Ohlinger R. Diagnostic value of palpation, mammography, and ultrasonography in the diagnosis of fibroadenoma: impact of breast density, patient age, ultrasonographic size, and palpability. Ultraschall Med 2012; 33:e151–e157. doi: 10.1055/s-0031-1273410.
    24. Xiang W, Huang Z, Tang C, Shen B, Yu Q, Niu X, et al. Use of ultrasound combined with magnetic resonance imaging for diagnosis of breast masses and fibroids. J Int Med Res 2019; 47:3070–3078. doi: 10.1177/0300060519848611.
    25. Pillay S, Cheddie S, Moodley Y. Fibroadenoma of the breast in a South African population – a pilot study of the diagnostic accuracy of fine needle aspirate cytology and breast ultrasonography. Afr Health Sci 2018; 18:273–280. doi: 10.4314/ahs.v18i2.11.
    26. Walters TK, Zuckerman J, Nisbet-Smith A, Hudson E, Chia Y, Burke M. Fine needle aspiration biopsy in the diagnosis and management of fibroadenoma of the breast. Br J Surg 1990; 77:1215–1217. doi: 10.1002/bjs.1800771107.
    27. Malberger E, Yerushalmi R, Tamir A, Keren R. Diagnosis of fibroadenoma in breast fine needle aspirates devoid of typical stroma. Acta Cytol 1997; 41:1483–1488. doi: 10.1159/000332863.
    28. Kollur SM, El Hag IA. FNA of breast fibroadenoma: observer variability and review of cytomorphology with cytohistological correlation. Cytopathology 2006; 17:239–244. doi: 10.1111/j.1365-2303.2006.00360.x.
    29. Salvadori B, Cusumano F, Del Bo R, Delledonne V, Grassi M, Rovini D, et al. Surgical treatment of phyllodes tumors of the breast. Cancer 1989; 63:2532–2536. doi: 10.1002/1097-0142(19890615)63:12<2532::aid-cncr2820631229>3.0.co;2-q.
    30. Tan PH, Thike AA, Tan WJ, Thu MM, Busmanis I, Li H, et al. Predicting clinical behaviour of breast phyllodes tumours: a nomogram based on histological criteria and surgical margins. J Clin Pathol 2012; 65:69–76. doi: 10.1136/jclinpath-2011-200368.
    31. Slodkowska E, Nofech-Mozes S, Xu B, Parra-Herran C, Lu FI, Raphael S, et al. Fibroepithelial lesions of the breast: a comprehensive morphological and outcome analysis of a large series. Mod Pathol 2018; 31:1073–1084. doi: 10.1038/s41379-018-0032-8.
    32. Gordon PB, Gagnon FA, Lanzkowsky L. Solid breast masses diagnosed as fibroadenoma at fine-needle aspiration biopsy: acceptable rates of growth at long-term follow-up. Radiology 2003; 229:233–238. doi: 10.1148/radiol.2291010282.
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