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The role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography in the differential diagnosis of pericardial disease

This study aimed to assess the role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography ((18)FDG-PET/CT) in the differential diagnosis of pericardial disease. The diagnosis is often troublesome because pericardial fluid analysis or biopsy does not always provide answers. (18...

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Autores principales: Hyeon, Cheol Won, Yi, Hyun Kyung, Kim, Eun Kyoung, Park, Sung-Ji, Lee, Sang-Chol, Park, Seung Woo, Oh, Jae K., Choi, Joon Young, Chang, Sung-A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726568/
https://www.ncbi.nlm.nih.gov/pubmed/33299053
http://dx.doi.org/10.1038/s41598-020-78581-y
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author Hyeon, Cheol Won
Yi, Hyun Kyung
Kim, Eun Kyoung
Park, Sung-Ji
Lee, Sang-Chol
Park, Seung Woo
Oh, Jae K.
Choi, Joon Young
Chang, Sung-A
author_facet Hyeon, Cheol Won
Yi, Hyun Kyung
Kim, Eun Kyoung
Park, Sung-Ji
Lee, Sang-Chol
Park, Seung Woo
Oh, Jae K.
Choi, Joon Young
Chang, Sung-A
author_sort Hyeon, Cheol Won
collection PubMed
description This study aimed to assess the role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography ((18)FDG-PET/CT) in the differential diagnosis of pericardial disease. The diagnosis is often troublesome because pericardial fluid analysis or biopsy does not always provide answers. (18)FDG-PET/CT can visualize both inflammation and malignancy and offers a whole-body assessment. Patients who visited the Pericardial Disease Clinic of Samsung Medical Center with an (18)FDG-PET/CT order code were extracted. Exclusion criteria were as follows: (1) the purpose of the differential diagnosis was not pericardial disease; (2) the patient had a known advanced-stage malignancy; (3) the patient already have confirmative diagnosis using a serology, pericardial effusion analysis or biopsy. The analysis included 107 patients. The most common final diagnosis was idiopathic (n = 46, 43.0%), followed by tuberculosis (n = 30, 28.0%) and neoplastic (n = 11, 10.3%). A maximum standardized uptake value (SUVmax) ≥ 5 typically indicates tuberculosis or neoplastic pericarditis except in just one case of autoimmune pericarditis); especially all of the SUVmax scores ≥ 10 had tuberculosis. The diagnostic yield of pericardial biopsy was very low (10.2%). Interestingly, all of the pericardium with an SUVmax < 4.4 had nondiagnostic results. In contrast, targeted biopsies based on (18)FDG uptake demonstrated a higher diagnostic yield (38.7%) than pericardium. The sensitivity of (18)FDG-PET/CT was 63.6%. The specificity was 71.9%. The positive predictive value was 20.6%. The negative predictive value 94.5%, and the accuracy was 71.0% for excluding malignancy based upon the FDG uptake patterns. It is possible to explore the differential diagnosis in some patients with difficult pericardiocentesis or pericardial biopsy in a noninvasive manner using on the SUVmax or uptake patterns. In addition, the biopsy strategy depending on (18)FDG uptake is helpful to achieve biopsy more safely and with a higher yield. (18)FDG-PET may enhance the diagnostic efficacy in patients with pericardial disease.
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spelling pubmed-77265682020-12-14 The role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography in the differential diagnosis of pericardial disease Hyeon, Cheol Won Yi, Hyun Kyung Kim, Eun Kyoung Park, Sung-Ji Lee, Sang-Chol Park, Seung Woo Oh, Jae K. Choi, Joon Young Chang, Sung-A Sci Rep Article This study aimed to assess the role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography ((18)FDG-PET/CT) in the differential diagnosis of pericardial disease. The diagnosis is often troublesome because pericardial fluid analysis or biopsy does not always provide answers. (18)FDG-PET/CT can visualize both inflammation and malignancy and offers a whole-body assessment. Patients who visited the Pericardial Disease Clinic of Samsung Medical Center with an (18)FDG-PET/CT order code were extracted. Exclusion criteria were as follows: (1) the purpose of the differential diagnosis was not pericardial disease; (2) the patient had a known advanced-stage malignancy; (3) the patient already have confirmative diagnosis using a serology, pericardial effusion analysis or biopsy. The analysis included 107 patients. The most common final diagnosis was idiopathic (n = 46, 43.0%), followed by tuberculosis (n = 30, 28.0%) and neoplastic (n = 11, 10.3%). A maximum standardized uptake value (SUVmax) ≥ 5 typically indicates tuberculosis or neoplastic pericarditis except in just one case of autoimmune pericarditis); especially all of the SUVmax scores ≥ 10 had tuberculosis. The diagnostic yield of pericardial biopsy was very low (10.2%). Interestingly, all of the pericardium with an SUVmax < 4.4 had nondiagnostic results. In contrast, targeted biopsies based on (18)FDG uptake demonstrated a higher diagnostic yield (38.7%) than pericardium. The sensitivity of (18)FDG-PET/CT was 63.6%. The specificity was 71.9%. The positive predictive value was 20.6%. The negative predictive value 94.5%, and the accuracy was 71.0% for excluding malignancy based upon the FDG uptake patterns. It is possible to explore the differential diagnosis in some patients with difficult pericardiocentesis or pericardial biopsy in a noninvasive manner using on the SUVmax or uptake patterns. In addition, the biopsy strategy depending on (18)FDG uptake is helpful to achieve biopsy more safely and with a higher yield. (18)FDG-PET may enhance the diagnostic efficacy in patients with pericardial disease. Nature Publishing Group UK 2020-12-09 /pmc/articles/PMC7726568/ /pubmed/33299053 http://dx.doi.org/10.1038/s41598-020-78581-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hyeon, Cheol Won
Yi, Hyun Kyung
Kim, Eun Kyoung
Park, Sung-Ji
Lee, Sang-Chol
Park, Seung Woo
Oh, Jae K.
Choi, Joon Young
Chang, Sung-A
The role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography in the differential diagnosis of pericardial disease
title The role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography in the differential diagnosis of pericardial disease
title_full The role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography in the differential diagnosis of pericardial disease
title_fullStr The role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography in the differential diagnosis of pericardial disease
title_full_unstemmed The role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography in the differential diagnosis of pericardial disease
title_short The role of (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography in the differential diagnosis of pericardial disease
title_sort role of (18)f-fluorodeoxyglucose-positron emission tomography/computed tomography in the differential diagnosis of pericardial disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726568/
https://www.ncbi.nlm.nih.gov/pubmed/33299053
http://dx.doi.org/10.1038/s41598-020-78581-y
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