Isolated radial scar diagnosis by core-needle biopsy: Is surgical excision necessary?
© Kim et al. 2016
Received: 8 March 2016
Accepted: 10 March 2016
Published: 31 March 2016
Radial scar and radial sclerosis (RS) are considered benign breast lesions with proliferative features. There is sparse literature on frequency of cancer upgrade in these patients without atypical features found on image-guided needle biopsy. This study retrospectively reviews cases of isolated RS diagnosed on needle biopsy and evaluates the cancer upgrade after subsequent surgical excision.
We conducted a retrospective cross-sectional study of cases with an isolated RS diagnosis based on needle biopsy and subsequent surgical pathology among all patients between January 1, 2009 and December 31, 2013. Patients with concomitant atypia, lobular carcinoma in situ on core biopsy, complete excision of very small RS with needle biopsy, and radiology-pathology discordance were excluded. An upgrade from the needle biopsy of RS was defined as surgical excision pathology that revealed ductal carcinoma in situ (DCIS), invasive ductal carcinoma (IDC), and/or invasive lobular carcinoma (ILC).
10,921 image-guided needle biopsy pathology reports were collected and 88 patients (0.81 %) were identified as having isolated RS. Of these 88 patients, 63 (72 %) underwent excision. The upgrade rate to cancer on subsequent surgical excision was 1.59 % (1/63) for DCIS; 0 % (0/63) for IDC; and 0 % (0/63) ILC. Twenty-five patients who did not undergo surgical excision had stable imaging studies with mean (±SD) 26 (±20) months follow up.
Isolated radial scar on needle biopsy may not warrant routine surgical excision given relatively low cancer upgrade rates. Advancement in breast imaging, pathology and multidisciplinary approaches to care may effectively guide non-surgical management of RS.
Breast cancer is the most common cancer diagnosed and the second leading cause of cancer-related deaths in women in the United States (Howlader et al. 2011). Women with a history of benign breast disease (BBD) are at an increased risk for developing breast cancer. A well-established BBD classification system was developed by Dupont and Page, which consists of (1) non-proliferative disease, (2) proliferative disease without atypia, and (3) proliferative disease with atypia (Dupont and Page 1985). Dupont and Page, and others reviewed more than 10,000 benign breast biopsies and they found that women with BBD with atypia had a breast cancer relative risk 4.4 times higher than that of the general population (Dupont and Page 1985; Degnim et al. 2007; Morgan et al. 2012).
Quantifying the risk of breast cancer of proliferative disease without atypia has been an ongoing challenge (Degnim et al. 2007; Morgan et al. 2012; Krishnamurthy et al. 2012). The lack of consensus on management of these patients with benign and high risk breast disease can be demonstrated by a survey taken by the American Society of Breast Surgeons in 2011 (Krishnamurthy et al. 2012). Approximately 1020 practicing breast surgeons were asked about their preferred management of these breast lesions, including atypical lobular hyperplasia, atypical ductal hyperplasia, lobular carcinoma in situ (LCIS), flat epithelial atypia, radial scar and papilloma without atypia (Krishnamurthy et al. 2012). Surgical excision biopsy was recommended for most patients when needle core biopsy showed these high risk lesions were present. Surgical excisional biopsy was recommended in approximately 63 % of cases for papilloma without atypia, 75 % for atypical lobular hyperplasia, 70 % for LCIS, 72 % for flat epithelial atypia, and 76 % for radial scar (Krishnamurthy et al. 2012). These variations of practice pattern are due to lack of robust research outcome studies.
The purpose of this study is to retrospectively review isolated RS diagnosis found on image-guided percutaneous core needle biopsies, and determine cancer upgrade after subsequent surgical excision.
This study was reviewed and approved by the Sutter Health Central Area Institutional Review Committee (IRC). We also obtained administrative and institutional approval from the approved study site(s), including Roseville, Sacramento, Davis, Auburn, Amador, Solano, and Yuba City. Data was obtained through a query of the Sutter electronic medical record system (EPIC), and Diagnostic Pathology Medical Group (DPMG) electronic medical database (Claris) to establish the cases meeting the study inclusion criteria. Patient paper charts were retrieved to extract information not available in electronic medical records.
The study design was retrospective and observational. Our study utilized available aggregate database analysis from EPIC, DPMG and patient charts to obtain patient demographic and medical history. Adult females who underwent needle biopsy at Sutter Imaging Center from Jan 1, 2009 through Dec 31, 2013 were included. Core needle biopsy and surgical pathology results with diagnosis of isolated RS were analyzed. Exclusion criteria included male gender, previous ipsilateral cancer diagnosis 6 months prior to breast biopsy, patients with concomitant atypia or LCIS on core biopsy, complete excision of very small RS with core needle biopsy and radiology-pathology discordance. An upgrade from the core biopsy of isolated RS was defined as surgical excision pathology that revealed ductal carcinoma in situ (DCIS), invasive ductal carcinoma (IDC), and/or invasive lobular carcinoma (ILC).
To evaluate the impact of needle size and upgrade in cancer, the size (gauge) of the core needle and the type of image technology were noted. Breast lesions biopsied stereotactically were obtained with the use of the 14, 11 and 8 gauge vacuum assisted device (Hologic, Marlborough, MA). Stereotatic biopsies were performed while the patient lay prone on a dedicated stereotactic table (Hologic, Marlborough, MA). Ultrasound guided biopsy (Bard, Murray Hill, NJ) and Breast MRI guided biopsy (Hologic, Marlborough, MA) were used. After core samples were obtained, a small biopsy marker (Hologic, Marlborough, MA) was placed at the site of the biopsy.
A combined database containing demographic data, family history of breast cancer, alcohol/tobacco use, body mass index (BMI), pathology, and breast density was obtained by linking the EPIC/Clarity and DPMG/Claris databases by patient name and date of birth. Missing values were obtained by EPIC chart review. Cases of radial scar were filtered from the pathology report and validated by chart review.
Descriptive statistics were used to examine and explore the data. Chi square Test of Independence (categorical variables) and analysis of variance (continuous variables) were used to compare differences between the excision and non-excision groups. P values less than 0.05 were considered statistically significant.
We identified 10,921 image-guided core needle biopsy breast pathology reports from the years 2009 through 2013, of which 88 patients (0.81 %) were identified as having isolated RS diagnosis with radiology-pathology concordance. All 88 patients were recommended for surgical excision by the pathologist and radiologist. Of the 88 patients, 63 (72 %) underwent surgical excision, and 25 (28 %) did not undergo surgical excision after core biopsy.
Subject characteristics and risk factors
Those who underwent surgical excision (n = 63)
Those who did not undergo surgical excision (n = 25)
Family history—n (%)
American Indian/Alaska Native
Active alcohol use—n (%)
Density, mammographic—n (%)
Imaging and core biopsy characteristics of patients who did not undergo surgery
Initial detection imaging type
Type of abnormality
Size of abnormality (mm)
Screening (n = 21)
Cluster of calcifications (n = 9)
Mass (n = 7)
Architectural distortion (n = 2)
Unknown (n = 3)
High risk patient screening (n = 4)
Enhancing nodule (n = 1)
Non-mass like enhancement (n = 1)
Unknown (n = 2)
Needle size (n = 16)
Type of core biopsy needle
Number of core biopsy samples
14 gauge needle
11 gauge needle
9 gauge needle
6 (4-Vac and 2-nonVac)
Unknown size (n = 9)
Cancer upgrade case after surgical excision
Caliber of needle
Architectural distortion (17 mm)
MRI guided Vacuum Assisted
In the modern era of medicine, replacing surgical biopsy with image-guided core needle biopsy for non-palpable lesions initially discovered on screening is no longer controversial. The American College of Surgeons Commission on Cancer strongly supports this change in clinical practice. However, controversy still exists regarding when to surgically excise the residual lesion once core needle biopsy reveals proliferative benign breast disease, especially isolated RS. Spiculated radiologic characteristics of RS resemble malignancy, and it can be challenging to differentiate between this and tubular histotype carcinoma (López-Medina et al. 2006). Current literature on cancer upgrade rate after surgical excision widely varies from 0 to 40 % due to heterogeneous study patient populations, including mixture of isolated RS and RS with atypia lesions, study patient populations combining RS diagnosis from both core and upfront surgical excision biopsy, small study sample sizes, and lack of comparison between patients who did and did not undergo surgery (Resetkova et al. 2011; Linda et al. 2010; Sohn et al. 2010; Doyle et al. 2007; Douglas-Jones et al. 2007; Berg et al. 2008; Becker et al. 2006; Cawson et al. 2003; Brenner et al. 2002). Our study contributes to the literature by (1) evaluating a patient population consisting of only isolated RS without atypia and (2) comparing patients who did and did not undergo surgery after core needle biopsy. Sutter Medical Centers of Sacramento Sierra region serves over a million residents in both urban and suburban areas. The Sacramento Metropolitan Area is the largest in the Central Valley and the fourth largest in the state, and these service regions combined represents a study population that is generalizable to residents of northern California.
The cancer upgrade rates after surgery in our patient population with isolated RS found on core needle biopsy was 1.59 % (1/63) for DCIS. The histologic feature of DCIS was clearly different from tubular histotype histologically. There was no invasive carcinoma cancer upgrade.
The relatively low malignancy upgrade rate in this study supports the clinical judgment in favor of using large bore vacuum assisted core needle biopsy size, sampling at least 6 cores in the setting of lesion size less than 2 cm, and performing post biopsy re-imaging to evaluate residual disease after the core needle biopsy has been performed. If there is notable residual disease present or discordance, then surgical excision should be performed. Post biopsy residual disease on post biopsy imaging would be concerning for sampling error risk as studies suggest that the proportion of radial scar volume involved by carcinoma ranges from 3.7 to 16.2 % and carcinoma involved the periphery of the lesion (López-Medina et al. 2006).
Our radiologists perform approximately 4–6 core samples per lesion. On the other hand, Brenner et al. (2002) and Becker et al. (2006) recommends at least 12 core specimens using vacuum assisted large core needles (11 or 14 gauge) to achieve reliable samples. This difference is due to difference in patient population. Our patient population consists of radiological lesions with size less than 2 cm. Between 4 and 6 core samples for lesions less than 2 cm in size may be reliable based on our study findings, and is clinically outweighed by higher risk of bleeding, larger hematoma, and pain associated with greater number of core sampling case by case basis. This question requires further study in larger samples.
Finally, it is important to consider the 63 patients who underwent surgery who did not have cancer. While knowledge that the residual area has been completely excised and therefore ruled out for cancer is highly beneficial, it is also very important to question in what ways we are over-treating our patient population. There are potential complications associated with surgery such as wound dehiscence, infection, hematoma and pain. Also there are potential complications from anesthesia. There are personal costs, such as anxiety with associated surgery. Additional research studies to quantify these impacts is needed as well as additional study in other populations, such as different socio-demographic patient populations, different approaches to handling RS lesions, and different RS lesions radiologic presentations.
Isolated RS management recommendations
Surgical excisional biopsy recommendation
Imaging follow-up recommendation
Associated atypia or LCIS
Isolated RS <2 cm size
Concordance of radiology/pathology
Limited sampling (large lesion, bleeding during biopsy, notable residual disease)
No atypia or LCIS
Associated mass on US or breast MRI
EMHK—study design, collection, analysis and interpretation of data, and writing the manuscript. AH—study collection analysis and interpretation of data and writing the manuscript. DM and BW—study analysis and interpretation of data. JC—study collection, analysis and interpretation of data. RR—study collection. SD—study analysis. CS—study analysis and interpretation of data, and writing the manuscript. All authors read and approved the final manuscript.
We are indebted to Carol Parise Ph.D., statistician at Sutter Research Institute of Medical Research, for her statistical expertise. We are also grateful to David Earle for his administration support.
All authors declare that they have no competing interests, except for Dr. Claire Synder. She has received research funding from Genetech and Anthem through Johns Hopkins University, Stock ownership from Immunomedics, and served as consultant to Pfizer.
This study was funded by Grant 947110-1107563 from the Sutter Medical Center Foundation.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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