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Radiological and clinical findings in sclerosing adenosis of the breast

To study the imaging and clinical features of breast sclerosing adenosis (SA), and to enhance the recognition of this disease, as well as to help the clinic to give a correct diagnosis. Imaging findings were retrospectively reviewed in 47 women with SA lesions confirmed by pathology (including 39 ca...

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Autores principales: Tan, Hongna, Zhang, Huiyu, Lei, Zhidan, Fu, Fangfang, Wang, Meiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775334/
https://www.ncbi.nlm.nih.gov/pubmed/31574804
http://dx.doi.org/10.1097/MD.0000000000017061
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author Tan, Hongna
Zhang, Huiyu
Lei, Zhidan
Fu, Fangfang
Wang, Meiyun
author_facet Tan, Hongna
Zhang, Huiyu
Lei, Zhidan
Fu, Fangfang
Wang, Meiyun
author_sort Tan, Hongna
collection PubMed
description To study the imaging and clinical features of breast sclerosing adenosis (SA), and to enhance the recognition of this disease, as well as to help the clinic to give a correct diagnosis. Imaging findings were retrospectively reviewed in 47 women with SA lesions confirmed by pathology (including 39 cases of mammography, 40 cases of ultrasound [US], and 34 cases magnetic resonance imaging [MRI]). Of 47 patients confirmed with SA, 18 cases were pure SA, and 29 cases coexist with other proliferative lesions and malignancies; the maximum diameter of SA lesions was 0.5 to 3.5 cm with an average of 1.6 cm. On the mammogram of 39 SA cases, the percentage of architectural distortion, calcifications, mass/nodular, asymmetric density, and mass combining with calcifications were 30.8%, 23.1%, 17.9%, 12.8%, and 7.7%, respectively; and 3 cases had no abnormal findings. On the sonogram (excluding 5 normal finding cases), the majority of lesions showed regular shaped (57.1%), well defined margined (60.0%), heterogenous low echoed (71.4%) nodulus. 85.3% lesions showed high signal on T2-weighted images, and all lesions were enhanced markedly, including 82.4% lesions appearing mass-like enhancement (17 star-shaped enhanced masses included); and the percentage of the time-signal intensity curve in type 1, type 2, and type 3 were 52.9%, 41.2%, and 5.9%, respectively. If the category breast imaging-reporting and data system ≥4b was considered to be a suspicious malignant lesion, the misdiagnostic rates of mammography, US, and MRI would be 17.9%, 17.5%, and 35.3%, respectively. The SA lesions are small and can occur with other diseases histologically. The majority of SA lesions showed distortion or calcifications on mammograms, low echo-level nodules with heterogenous echo on US and mass-like lesion with or without star shape on enhanced MRI.
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spelling pubmed-67753342019-10-07 Radiological and clinical findings in sclerosing adenosis of the breast Tan, Hongna Zhang, Huiyu Lei, Zhidan Fu, Fangfang Wang, Meiyun Medicine (Baltimore) 5750 To study the imaging and clinical features of breast sclerosing adenosis (SA), and to enhance the recognition of this disease, as well as to help the clinic to give a correct diagnosis. Imaging findings were retrospectively reviewed in 47 women with SA lesions confirmed by pathology (including 39 cases of mammography, 40 cases of ultrasound [US], and 34 cases magnetic resonance imaging [MRI]). Of 47 patients confirmed with SA, 18 cases were pure SA, and 29 cases coexist with other proliferative lesions and malignancies; the maximum diameter of SA lesions was 0.5 to 3.5 cm with an average of 1.6 cm. On the mammogram of 39 SA cases, the percentage of architectural distortion, calcifications, mass/nodular, asymmetric density, and mass combining with calcifications were 30.8%, 23.1%, 17.9%, 12.8%, and 7.7%, respectively; and 3 cases had no abnormal findings. On the sonogram (excluding 5 normal finding cases), the majority of lesions showed regular shaped (57.1%), well defined margined (60.0%), heterogenous low echoed (71.4%) nodulus. 85.3% lesions showed high signal on T2-weighted images, and all lesions were enhanced markedly, including 82.4% lesions appearing mass-like enhancement (17 star-shaped enhanced masses included); and the percentage of the time-signal intensity curve in type 1, type 2, and type 3 were 52.9%, 41.2%, and 5.9%, respectively. If the category breast imaging-reporting and data system ≥4b was considered to be a suspicious malignant lesion, the misdiagnostic rates of mammography, US, and MRI would be 17.9%, 17.5%, and 35.3%, respectively. The SA lesions are small and can occur with other diseases histologically. The majority of SA lesions showed distortion or calcifications on mammograms, low echo-level nodules with heterogenous echo on US and mass-like lesion with or without star shape on enhanced MRI. Wolters Kluwer Health 2019-09-27 /pmc/articles/PMC6775334/ /pubmed/31574804 http://dx.doi.org/10.1097/MD.0000000000017061 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 5750
Tan, Hongna
Zhang, Huiyu
Lei, Zhidan
Fu, Fangfang
Wang, Meiyun
Radiological and clinical findings in sclerosing adenosis of the breast
title Radiological and clinical findings in sclerosing adenosis of the breast
title_full Radiological and clinical findings in sclerosing adenosis of the breast
title_fullStr Radiological and clinical findings in sclerosing adenosis of the breast
title_full_unstemmed Radiological and clinical findings in sclerosing adenosis of the breast
title_short Radiological and clinical findings in sclerosing adenosis of the breast
title_sort radiological and clinical findings in sclerosing adenosis of the breast
topic 5750
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775334/
https://www.ncbi.nlm.nih.gov/pubmed/31574804
http://dx.doi.org/10.1097/MD.0000000000017061
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