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Idiopathic granulomatous mastitis: imaging update and review

OBJECTIVES: The purpose of this study was to review the imaging features of idiopathic granulomatous mastitis (IGM) with clinical and pathology correlation. METHODS: With institutional review board (IRB) approval, a retrospective search of the surgical pathology database from January 2000 to July 20...

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Autores principales: Fazzio, Robert T., Shah, Sejal S., Sandhu, Nicole P., Glazebrook, Katrina N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956627/
https://www.ncbi.nlm.nih.gov/pubmed/27221974
http://dx.doi.org/10.1007/s13244-016-0499-0
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author Fazzio, Robert T.
Shah, Sejal S.
Sandhu, Nicole P.
Glazebrook, Katrina N.
author_facet Fazzio, Robert T.
Shah, Sejal S.
Sandhu, Nicole P.
Glazebrook, Katrina N.
author_sort Fazzio, Robert T.
collection PubMed
description OBJECTIVES: The purpose of this study was to review the imaging features of idiopathic granulomatous mastitis (IGM) with clinical and pathology correlation. METHODS: With institutional review board (IRB) approval, a retrospective search of the surgical pathology database from January 2000 to July 2015 was performed. Clinical, imaging and histology findings were reviewed. Cases of granulomatous mastitis without a known source, diagnosed with percutaneous or surgical biopsy, were included in our analysis. RESULTS: Seventeen cases of IGM were identified with imaging available for review. The majority of patients presented with a palpable abnormality, whereas a minority were asymptomatic with an abnormal screening mammogram. At imaging, IGM most often demonstrated a focal asymmetry at mammography, a hypoechoic mass with irregular or angular margins at ultrasound, and robust enhancement with mixed progressive and plateau kinetics at magnetic resonance imaging (MRI). Axillary lymph nodes were reactive in appearance at ultrasound. Molecular breast imaging performed in one case showed mild focal asymmetric radiotracer uptake. CONCLUSION: IGM is a rapidly progressive rare inflammatory condition of the breast resulting in non-necrotizing granuloma formation. Imaging features mimic breast carcinoma and diagnosis can be difficult. Radiologists’ awareness of this condition is essential to prevent delayed or unnecessary treatment. TEACHING POINTS: • Idiopathic granulomatous mastitis is rapidly progressive inflammatory condition. • Imaging features may mimic breast carcinoma or infection. • Ultrasound shows irregular hypoechoic masses with increased vascularity and sinus tracts. • MRI shows irregular, enhancing masses or non-mass enhancement with microabscesses. • MRI is useful for assessment of breast involvement and response to treatment.
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spelling pubmed-49566272016-08-01 Idiopathic granulomatous mastitis: imaging update and review Fazzio, Robert T. Shah, Sejal S. Sandhu, Nicole P. Glazebrook, Katrina N. Insights Imaging Pictorial Review OBJECTIVES: The purpose of this study was to review the imaging features of idiopathic granulomatous mastitis (IGM) with clinical and pathology correlation. METHODS: With institutional review board (IRB) approval, a retrospective search of the surgical pathology database from January 2000 to July 2015 was performed. Clinical, imaging and histology findings were reviewed. Cases of granulomatous mastitis without a known source, diagnosed with percutaneous or surgical biopsy, were included in our analysis. RESULTS: Seventeen cases of IGM were identified with imaging available for review. The majority of patients presented with a palpable abnormality, whereas a minority were asymptomatic with an abnormal screening mammogram. At imaging, IGM most often demonstrated a focal asymmetry at mammography, a hypoechoic mass with irregular or angular margins at ultrasound, and robust enhancement with mixed progressive and plateau kinetics at magnetic resonance imaging (MRI). Axillary lymph nodes were reactive in appearance at ultrasound. Molecular breast imaging performed in one case showed mild focal asymmetric radiotracer uptake. CONCLUSION: IGM is a rapidly progressive rare inflammatory condition of the breast resulting in non-necrotizing granuloma formation. Imaging features mimic breast carcinoma and diagnosis can be difficult. Radiologists’ awareness of this condition is essential to prevent delayed or unnecessary treatment. TEACHING POINTS: • Idiopathic granulomatous mastitis is rapidly progressive inflammatory condition. • Imaging features may mimic breast carcinoma or infection. • Ultrasound shows irregular hypoechoic masses with increased vascularity and sinus tracts. • MRI shows irregular, enhancing masses or non-mass enhancement with microabscesses. • MRI is useful for assessment of breast involvement and response to treatment. Springer Berlin Heidelberg 2016-05-24 /pmc/articles/PMC4956627/ /pubmed/27221974 http://dx.doi.org/10.1007/s13244-016-0499-0 Text en © The Author(s) 2016 Open Access This 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.
spellingShingle Pictorial Review
Fazzio, Robert T.
Shah, Sejal S.
Sandhu, Nicole P.
Glazebrook, Katrina N.
Idiopathic granulomatous mastitis: imaging update and review
title Idiopathic granulomatous mastitis: imaging update and review
title_full Idiopathic granulomatous mastitis: imaging update and review
title_fullStr Idiopathic granulomatous mastitis: imaging update and review
title_full_unstemmed Idiopathic granulomatous mastitis: imaging update and review
title_short Idiopathic granulomatous mastitis: imaging update and review
title_sort idiopathic granulomatous mastitis: imaging update and review
topic Pictorial Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956627/
https://www.ncbi.nlm.nih.gov/pubmed/27221974
http://dx.doi.org/10.1007/s13244-016-0499-0
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