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The value of adjacent vessel sign in malignant breast tumors

PURPOSE The aim of this study was to evaluate the prognostic quality of adjacent vessel sign (AVS) in malignant breast tumors by comparing it with classical prognostic pathological biomarkers and magnetic resonance imaging (MRI) findings. METHODS A total of 124 patients with 133 malignant lesions we...

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Autores principales: Çetinkaya, Ezra, Yıldız, Şeyma, Otçu, Hafize, Sharifov, Rasul, Yabul, Fatma Çelik, Alkan, Alpay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish Society of Radiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682586/
https://www.ncbi.nlm.nih.gov/pubmed/35997479
http://dx.doi.org/10.5152/dir.2022.211228
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author Çetinkaya, Ezra
Yıldız, Şeyma
Otçu, Hafize
Sharifov, Rasul
Yabul, Fatma Çelik
Alkan, Alpay
author_facet Çetinkaya, Ezra
Yıldız, Şeyma
Otçu, Hafize
Sharifov, Rasul
Yabul, Fatma Çelik
Alkan, Alpay
author_sort Çetinkaya, Ezra
collection PubMed
description PURPOSE The aim of this study was to evaluate the prognostic quality of adjacent vessel sign (AVS) in malignant breast tumors by comparing it with classical prognostic pathological biomarkers and magnetic resonance imaging (MRI) findings. METHODS A total of 124 patients with 133 malignant lesions were included. All the imaging was performed on a 1.5T Avanto scanner and the images were interpreted according to BI-RADS-MR® (fifth ed.) atlas. Maximum intensity projection (MIP) images were constructed from subtracted post-contrast images and were used to investigate AVS. Histopathological results and MRI findings were compared with AVS. RESULTS Interobserver agreement about AVS status was substantial (κ = 0.64). AVS positive lesions were significantly bigger in size (P < .001, AVS negative: median 12 mm, AVS positive: median 31 mm). AVS was significantly associated with increased Ki-67 index and axillary lymph node metastasis (P = .009 and P = .019, respectively). Between AVS and lymphovascular invasion (LVI), there was a trend toward positive relationship (P = .076). MRI findings of T2 hypointensity, peritumoral edema, irregular shape, non-homogeneous contrast enhancement, rapid early contrast enhancement, and skin infiltration showed significant positive relation with AVS (P < .001, P < .001, P < .001, P = .02, P = .021, and P = .021, respectively). AVS is found to be associated with increased Ki-67 index, axillary lymph node metastasis, and some MRI findings that point to malignancy or poor prognosis. CONCLUSION AVS indicates poor prognosis since it is related to axillary lymph node metastasis, increased Ki-67 index, LVI, peritumoral edema, rapid early contrast enhancement, increased background enhancement, skin extension, T2 hypointensity, non-homogeneous contrast enhancement, irregular lesion shape, and larger tumor size. AVS is an easy to use sign that shows substantial interobserver agreement.
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spelling pubmed-96825862022-12-02 The value of adjacent vessel sign in malignant breast tumors Çetinkaya, Ezra Yıldız, Şeyma Otçu, Hafize Sharifov, Rasul Yabul, Fatma Çelik Alkan, Alpay Diagn Interv Radiol Original Article PURPOSE The aim of this study was to evaluate the prognostic quality of adjacent vessel sign (AVS) in malignant breast tumors by comparing it with classical prognostic pathological biomarkers and magnetic resonance imaging (MRI) findings. METHODS A total of 124 patients with 133 malignant lesions were included. All the imaging was performed on a 1.5T Avanto scanner and the images were interpreted according to BI-RADS-MR® (fifth ed.) atlas. Maximum intensity projection (MIP) images were constructed from subtracted post-contrast images and were used to investigate AVS. Histopathological results and MRI findings were compared with AVS. RESULTS Interobserver agreement about AVS status was substantial (κ = 0.64). AVS positive lesions were significantly bigger in size (P < .001, AVS negative: median 12 mm, AVS positive: median 31 mm). AVS was significantly associated with increased Ki-67 index and axillary lymph node metastasis (P = .009 and P = .019, respectively). Between AVS and lymphovascular invasion (LVI), there was a trend toward positive relationship (P = .076). MRI findings of T2 hypointensity, peritumoral edema, irregular shape, non-homogeneous contrast enhancement, rapid early contrast enhancement, and skin infiltration showed significant positive relation with AVS (P < .001, P < .001, P < .001, P = .02, P = .021, and P = .021, respectively). AVS is found to be associated with increased Ki-67 index, axillary lymph node metastasis, and some MRI findings that point to malignancy or poor prognosis. CONCLUSION AVS indicates poor prognosis since it is related to axillary lymph node metastasis, increased Ki-67 index, LVI, peritumoral edema, rapid early contrast enhancement, increased background enhancement, skin extension, T2 hypointensity, non-homogeneous contrast enhancement, irregular lesion shape, and larger tumor size. AVS is an easy to use sign that shows substantial interobserver agreement. Turkish Society of Radiology 2022-09-01 /pmc/articles/PMC9682586/ /pubmed/35997479 http://dx.doi.org/10.5152/dir.2022.211228 Text en © Copyright 2022 authors https://creativecommons.org/licenses/by-nc/4.0/ Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Original Article
Çetinkaya, Ezra
Yıldız, Şeyma
Otçu, Hafize
Sharifov, Rasul
Yabul, Fatma Çelik
Alkan, Alpay
The value of adjacent vessel sign in malignant breast tumors
title The value of adjacent vessel sign in malignant breast tumors
title_full The value of adjacent vessel sign in malignant breast tumors
title_fullStr The value of adjacent vessel sign in malignant breast tumors
title_full_unstemmed The value of adjacent vessel sign in malignant breast tumors
title_short The value of adjacent vessel sign in malignant breast tumors
title_sort value of adjacent vessel sign in malignant breast tumors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682586/
https://www.ncbi.nlm.nih.gov/pubmed/35997479
http://dx.doi.org/10.5152/dir.2022.211228
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