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Case of isolated cardiac sarcoidosis diagnosed by newly developed abnormal uptake during serial follow‐up fluorine‐18 fluorodeoxyglucose positron emission tomography
Cardiac sarcoidosis (CS) causes lethal arrhythmia and heart failure and has a poor prognosis; therefore, early detection and early stage treatment are important. However, diagnosis of isolated CS may be difficult in some cases owing to the low sensitivity of myocardial biopsy. Herein, we describe th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676290/ https://www.ncbi.nlm.nih.gov/pubmed/31264810 http://dx.doi.org/10.1002/ehf2.12472 |
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author | Maeda, Daichi Kanzaki, Yumiko Fujita, Shuichi Inuyama, Maaya Takashima, Shogo Miyamura, Masatoshi Terasaki, Fumio Hoshiga, Masaaki |
author_facet | Maeda, Daichi Kanzaki, Yumiko Fujita, Shuichi Inuyama, Maaya Takashima, Shogo Miyamura, Masatoshi Terasaki, Fumio Hoshiga, Masaaki |
author_sort | Maeda, Daichi |
collection | PubMed |
description | Cardiac sarcoidosis (CS) causes lethal arrhythmia and heart failure and has a poor prognosis; therefore, early detection and early stage treatment are important. However, diagnosis of isolated CS may be difficult in some cases owing to the low sensitivity of myocardial biopsy. Herein, we describe the case of a patient with isolated CS, showing change from negative to positive fluorine‐18 fluorodeoxyglucose ((18)F‐FDG) positron emission tomography (PET) uptake results within 9 months. The patient showed rapid reduction in left ventricular systolic function with sustained ventricular tachycardia. The diagnosis of isolated CS is often under‐recognized in clinical practice because it commonly requires the diagnosis of extracardiac disease in the absence of a positive endomyocardial biopsy. The Japanese Circulation Society recently published guidelines for CS diagnosis stating that isolated CS can be clinically diagnosed with positive (18)F‐FDG PET or (67)Gallium result. In this case, serial follow‐up (18)F‐FDG PET was useful for diagnosing isolated CS. |
format | Online Article Text |
id | pubmed-6676290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66762902019-08-06 Case of isolated cardiac sarcoidosis diagnosed by newly developed abnormal uptake during serial follow‐up fluorine‐18 fluorodeoxyglucose positron emission tomography Maeda, Daichi Kanzaki, Yumiko Fujita, Shuichi Inuyama, Maaya Takashima, Shogo Miyamura, Masatoshi Terasaki, Fumio Hoshiga, Masaaki ESC Heart Fail Case Reports Cardiac sarcoidosis (CS) causes lethal arrhythmia and heart failure and has a poor prognosis; therefore, early detection and early stage treatment are important. However, diagnosis of isolated CS may be difficult in some cases owing to the low sensitivity of myocardial biopsy. Herein, we describe the case of a patient with isolated CS, showing change from negative to positive fluorine‐18 fluorodeoxyglucose ((18)F‐FDG) positron emission tomography (PET) uptake results within 9 months. The patient showed rapid reduction in left ventricular systolic function with sustained ventricular tachycardia. The diagnosis of isolated CS is often under‐recognized in clinical practice because it commonly requires the diagnosis of extracardiac disease in the absence of a positive endomyocardial biopsy. The Japanese Circulation Society recently published guidelines for CS diagnosis stating that isolated CS can be clinically diagnosed with positive (18)F‐FDG PET or (67)Gallium result. In this case, serial follow‐up (18)F‐FDG PET was useful for diagnosing isolated CS. John Wiley and Sons Inc. 2019-07-02 /pmc/articles/PMC6676290/ /pubmed/31264810 http://dx.doi.org/10.1002/ehf2.12472 Text en © 2019 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Reports Maeda, Daichi Kanzaki, Yumiko Fujita, Shuichi Inuyama, Maaya Takashima, Shogo Miyamura, Masatoshi Terasaki, Fumio Hoshiga, Masaaki Case of isolated cardiac sarcoidosis diagnosed by newly developed abnormal uptake during serial follow‐up fluorine‐18 fluorodeoxyglucose positron emission tomography |
title | Case of isolated cardiac sarcoidosis diagnosed by newly developed abnormal uptake during serial follow‐up fluorine‐18 fluorodeoxyglucose positron emission tomography |
title_full | Case of isolated cardiac sarcoidosis diagnosed by newly developed abnormal uptake during serial follow‐up fluorine‐18 fluorodeoxyglucose positron emission tomography |
title_fullStr | Case of isolated cardiac sarcoidosis diagnosed by newly developed abnormal uptake during serial follow‐up fluorine‐18 fluorodeoxyglucose positron emission tomography |
title_full_unstemmed | Case of isolated cardiac sarcoidosis diagnosed by newly developed abnormal uptake during serial follow‐up fluorine‐18 fluorodeoxyglucose positron emission tomography |
title_short | Case of isolated cardiac sarcoidosis diagnosed by newly developed abnormal uptake during serial follow‐up fluorine‐18 fluorodeoxyglucose positron emission tomography |
title_sort | case of isolated cardiac sarcoidosis diagnosed by newly developed abnormal uptake during serial follow‐up fluorine‐18 fluorodeoxyglucose positron emission tomography |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676290/ https://www.ncbi.nlm.nih.gov/pubmed/31264810 http://dx.doi.org/10.1002/ehf2.12472 |
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