Majority of flat epithelial atypia diagnosed on biopsy do not require surgical excision

The Breast ◽  
2018 ◽  
Vol 37 ◽  
pp. 13-17 ◽  
Author(s):  
Patrick Mun Yew Chan ◽  
Niketa Chotai ◽  
Eileen Shujuan Lai ◽  
Pei Yi Sin ◽  
Juliana Chen ◽  
...  
2014 ◽  
Vol 20 (6) ◽  
pp. 606-614 ◽  
Author(s):  
Vandana Dialani ◽  
Shambhavi Venkataraman ◽  
Gretchen Frieling ◽  
Stuart J. Schnitt ◽  
Tejas S. Mehta

2018 ◽  
Vol 31 (7) ◽  
pp. 1097-1106 ◽  
Author(s):  
Zulfia McCroskey ◽  
Nour Sneige ◽  
Carolyn R Herman ◽  
Ross A Miller ◽  
Luz A Venta ◽  
...  

The Breast ◽  
2014 ◽  
Vol 23 (4) ◽  
pp. 352-356 ◽  
Author(s):  
Vanessa L. Prowler ◽  
Jennifer E. Joh ◽  
Geza Acs ◽  
John V. Kiluk ◽  
Christine Laronga ◽  
...  

2020 ◽  
Vol 2 (4) ◽  
pp. 336-342
Author(s):  
Paula B Gordon ◽  
Emma Branch

Abstract Objective Whether the optimal management of pure flat epithelial atypia (FEA) found on core needle biopsy (CNB) specimens is surgical excision or imaging follow-up remains controversial. This study aimed to determine the upgrade rate to ductal carcinoma in situ (DCIS), invasive carcinoma or a high-risk lesion (atypical ductal hyperplasia, atypical lobular hyperplasia, or lobular carcinoma in situ), and it explored the relationship between a family history of breast cancer and the risk of upgrade. Methods Cases with pure FEA found on stereotactic CNB of microcalcifications between March 2011 to December 2017 were followed by excisional biopsy or periodic imaging. The proportion of cases upgraded to a high-risk lesion and the odds of upgrade as related to a family history of breast cancer were determined with 95% confidence intervals (CIs). Results We identified 622 cases of pure FEA; 101 (16.2%) underwent surgical excision and 269 (43.2%) had imaging follow-up of ≥ 24 months. There were no upgrades to DCIS or invasive cancer in any of these 370 individuals (0%), and 4.6% (17/370; 95% CI: 2.9%–7.2%) were upgraded to a high-risk lesion. There was a nonstatistically significant trend between family history and upgrade to high-risk lesion (odds ratio 1.72 [95% CI: 0.65%–4.57%]). Conclusion In our study, the upgrade rate of pure FEA to malignancy was 0%. We suggest that regular imaging follow-up is an appropriate alternative to surgery. Because of potential differences in biopsy techniques and pathologist interpretation of the primary biopsy, individual institutions should audit their own results prior to altering their management of FEA.


2010 ◽  
Vol 125 (1) ◽  
pp. 121-126 ◽  
Author(s):  
Vincent Lavoué ◽  
Claire Marie Roger ◽  
Mathieu Poilblanc ◽  
Nicolas Proust ◽  
Camille Monghal-Verge ◽  
...  

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