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PET/CT analysis of 21 patients with breast cancer: physiological distribution of (18)F-choline and diagnostic pitfalls
OBJECTIVES: (18)F-choline is a useful tracer for detecting tumours with high lipogenesis. Knowledge of its biodistribution pattern is essential to recognise physiological variants. The aim of this study was to describe the physiologic distribution of (18)F-choline and pitfalls in patients with breas...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134679/ https://www.ncbi.nlm.nih.gov/pubmed/29781364 http://dx.doi.org/10.1177/0300060518773019 |
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author | Ahmad Saad, Fathinul Fikri Zakaria, Mohd Hazeman Appanna, Bahunu |
author_facet | Ahmad Saad, Fathinul Fikri Zakaria, Mohd Hazeman Appanna, Bahunu |
author_sort | Ahmad Saad, Fathinul Fikri |
collection | PubMed |
description | OBJECTIVES: (18)F-choline is a useful tracer for detecting tumours with high lipogenesis. Knowledge of its biodistribution pattern is essential to recognise physiological variants. The aim of this study was to describe the physiologic distribution of (18)F-choline and pitfalls in patients with breast cancer. METHODS: Twenty-one consecutive patients with breast cancer (10 premenopausal and 11 postmenopausal women; mean age, 52.82 ± 10.71 years) underwent (18)F-choline positron emission tomography (PET)/computed tomography (CT) for staging. Whole-body PET/CT was acquired after 40 minutes of (18)F-choline uptake. Acquired PET images were measured semiquantitatively. RESULTS: All patients showed pitfalls unrelated to breast cancer. These findings were predominantly caused by physiological glandular uptake in the liver, spleen, pancreas, bowels, axial skeleton (85%-100%), inflammation and benign changes (4.76%), appendicular skeleton (4.76%–19.049%), and site contamination (61.9%). In <1%, a concomitant metastatic neoplasm was found. The breast showed higher physiological uptake in premenopausal compared with postmenopausal woman ((18)F-choline maximum standardised uptake values [g/dL] of the right breast = 2.04 ± 0.404 vs 1.59 ± 0.97 and left breast = 2.00 ± 0.56 vs 1.93 ± 1.28, respectively). CONCLUSION: (18)F-choline uptake was higher in premenopausal women. Physiological (18)F-choline uptake was observed in many sites, representing possible pathologies. |
format | Online Article Text |
id | pubmed-6134679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-61346792018-09-13 PET/CT analysis of 21 patients with breast cancer: physiological distribution of (18)F-choline and diagnostic pitfalls Ahmad Saad, Fathinul Fikri Zakaria, Mohd Hazeman Appanna, Bahunu J Int Med Res Clinical Research Reports OBJECTIVES: (18)F-choline is a useful tracer for detecting tumours with high lipogenesis. Knowledge of its biodistribution pattern is essential to recognise physiological variants. The aim of this study was to describe the physiologic distribution of (18)F-choline and pitfalls in patients with breast cancer. METHODS: Twenty-one consecutive patients with breast cancer (10 premenopausal and 11 postmenopausal women; mean age, 52.82 ± 10.71 years) underwent (18)F-choline positron emission tomography (PET)/computed tomography (CT) for staging. Whole-body PET/CT was acquired after 40 minutes of (18)F-choline uptake. Acquired PET images were measured semiquantitatively. RESULTS: All patients showed pitfalls unrelated to breast cancer. These findings were predominantly caused by physiological glandular uptake in the liver, spleen, pancreas, bowels, axial skeleton (85%-100%), inflammation and benign changes (4.76%), appendicular skeleton (4.76%–19.049%), and site contamination (61.9%). In <1%, a concomitant metastatic neoplasm was found. The breast showed higher physiological uptake in premenopausal compared with postmenopausal woman ((18)F-choline maximum standardised uptake values [g/dL] of the right breast = 2.04 ± 0.404 vs 1.59 ± 0.97 and left breast = 2.00 ± 0.56 vs 1.93 ± 1.28, respectively). CONCLUSION: (18)F-choline uptake was higher in premenopausal women. Physiological (18)F-choline uptake was observed in many sites, representing possible pathologies. SAGE Publications 2018-05-20 2018-08 /pmc/articles/PMC6134679/ /pubmed/29781364 http://dx.doi.org/10.1177/0300060518773019 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Clinical Research Reports Ahmad Saad, Fathinul Fikri Zakaria, Mohd Hazeman Appanna, Bahunu PET/CT analysis of 21 patients with breast cancer: physiological distribution of (18)F-choline and diagnostic pitfalls |
title | PET/CT analysis of 21 patients with breast cancer: physiological distribution of (18)F-choline and diagnostic pitfalls |
title_full | PET/CT analysis of 21 patients with breast cancer: physiological distribution of (18)F-choline and diagnostic pitfalls |
title_fullStr | PET/CT analysis of 21 patients with breast cancer: physiological distribution of (18)F-choline and diagnostic pitfalls |
title_full_unstemmed | PET/CT analysis of 21 patients with breast cancer: physiological distribution of (18)F-choline and diagnostic pitfalls |
title_short | PET/CT analysis of 21 patients with breast cancer: physiological distribution of (18)F-choline and diagnostic pitfalls |
title_sort | pet/ct analysis of 21 patients with breast cancer: physiological distribution of (18)f-choline and diagnostic pitfalls |
topic | Clinical Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134679/ https://www.ncbi.nlm.nih.gov/pubmed/29781364 http://dx.doi.org/10.1177/0300060518773019 |
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