pathologic correlation
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Author(s):  
Cameron J. Overfield ◽  
Mark A. Edgar ◽  
Daniel E. Wessell ◽  
Benjamin K. Wilke ◽  
Hillary W. Garner

Radiographics ◽  
2022 ◽  
Author(s):  
Leonardo P. Marcal ◽  
Venkateswar R. Surabhi ◽  
Nisha S. Ramani ◽  
Venkata S. Katabathina ◽  
Raj M. Paspulati ◽  
...  

Author(s):  
Kum Ju Chae ◽  
Myoung Ja Chung ◽  
Gong Yong Jin ◽  
Young Ju Song ◽  
Ae Ri An ◽  
...  

Author(s):  
Hoiwan Cheung ◽  
Elizabeth U Parker ◽  
Miao Yu ◽  
Mark R Kilgore ◽  
Diana L Lam

Author(s):  
Jorge Luis Huayanay Espinoza ◽  
Fiorela Noeli Mego Ramírez ◽  
Henry Guerra Miller ◽  
Mark Guelfguat

Radiographics ◽  
2021 ◽  
Author(s):  
Gabrielle Figueiredo ◽  
Aileen O'Shea ◽  
Grace Mary Neville ◽  
Susanna I. Lee

Author(s):  
Angela I Choe ◽  
Claudia Kasales ◽  
Julie Mack ◽  
Mayyadah Al-Nuaimi ◽  
Dipti M Karamchandani

Abstract Breast MRI provides high sensitivity but modest positive predictive value for identifying breast cancers, with approximately 75% of MRI-guided biopsies returning benign pathologies. Fibrocystic change (FCC) is a descriptive term used colloquially by many radiologists (and falling out of favor with many pathologists) to refer to several benign entities encountered in the breast. Many of the benign entities believed to comprise FCC can show enhancement on MRI. Recognizing the pathologic correlates of these enhancing lesions should help guide management after such a result on MRI-guided biopsy. Premenopausal women may present with clinical symptoms attributed to FCC, including pain, nipple discharge, breast lumps, or discrete masses. Benign entities associated with FCC include proliferative lesions such as usual ductal hyperplasia and sclerosing adenosis, and nonproliferative lesions including cysts, apocrine metaplasia, and stromal fibrosis. Fibrocystic change can be diffuse or focal. Diffuse FCC usually presents as non-mass enhancement (NME), often with persistent kinetics. Focal FCC can present as an irregular mass or focus with variable enhancement patterns including washout kinetics. Following a benign concordant MRI-guided biopsy result of one or more of the above entities, follow-up with MRI in 12 months is reasonable. Accurate radiologic–pathologic correlation can be achieved when careful review of histologic findings is carried out in the context of MRI features.


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