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Characteristics and Clinical Value of 18F-FDG PET/CT in the Management of Adult-Onset Still’s Disease: 35 Cases

While the diagnosis of adult-onset Still’s disease (AOSD) involves the exclusion of differential diagnoses, the characteristics and value of 18F-Fluorodeoxyglucose (18F-FDG) Positron Emission Tomography coupled with CT (PET/CT) in the management of AOSD remain poorly known. Our retrospective study i...

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Autores principales: Brisset, Josselin, Jamilloux, Yvan, Dumonteil, Stephanie, Lades, Guillaume, Killian, Martin, Gerfaud-Valentin, Mathieu, Lemaire, Anne, Chroboczek, Tomasz, Liozon, Eric, Gondran, Guillaume, Sève, Pascal, Monteil, Jacques, Fauchais, Anne-Laure, Ly, Kim Heang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200084/
https://www.ncbi.nlm.nih.gov/pubmed/34199846
http://dx.doi.org/10.3390/jcm10112489
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author Brisset, Josselin
Jamilloux, Yvan
Dumonteil, Stephanie
Lades, Guillaume
Killian, Martin
Gerfaud-Valentin, Mathieu
Lemaire, Anne
Chroboczek, Tomasz
Liozon, Eric
Gondran, Guillaume
Sève, Pascal
Monteil, Jacques
Fauchais, Anne-Laure
Ly, Kim Heang
author_facet Brisset, Josselin
Jamilloux, Yvan
Dumonteil, Stephanie
Lades, Guillaume
Killian, Martin
Gerfaud-Valentin, Mathieu
Lemaire, Anne
Chroboczek, Tomasz
Liozon, Eric
Gondran, Guillaume
Sève, Pascal
Monteil, Jacques
Fauchais, Anne-Laure
Ly, Kim Heang
author_sort Brisset, Josselin
collection PubMed
description While the diagnosis of adult-onset Still’s disease (AOSD) involves the exclusion of differential diagnoses, the characteristics and value of 18F-Fluorodeoxyglucose (18F-FDG) Positron Emission Tomography coupled with CT (PET/CT) in the management of AOSD remain poorly known. Our retrospective study included patients from four centers, fulfilling Yamaguchi or Fautrel criteria, who underwent a PET/CT during an active AOSD. Thirty-five patients were included. At the time of PET/CT, the Yamaguchi criteria were met in 23 of 29 evaluable cases. PET/CT showed bone marrow (74.3%), lymph node (74.3%), and splenic (48.6%) FDG uptake. Despite arthralgia or arthritis in most patients, joints were rarely the sites of 18F-FDG accumulation. The spatial distribution of 18F-FDG uptake was nonspecific, and its intensity could be similar to malignant disease. Lymph node or bone marrow biopsy was performed after PET/CT in 20 patients (57.1%). The intensity of bone marrow; splenic and lymph node hypermetabolism appeared to be correlated with disease activity. Abnormal PET/CT in the cervical lymph nodes and age ≥ 60 years seemed to be predictive factors for monocyclic evolution. The clinical value of PET/CT is not in direct diagnosis; but as an aid in excluding differential diagnoses by searching for their scintigraphic features and guiding biopsy.
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spelling pubmed-82000842021-06-14 Characteristics and Clinical Value of 18F-FDG PET/CT in the Management of Adult-Onset Still’s Disease: 35 Cases Brisset, Josselin Jamilloux, Yvan Dumonteil, Stephanie Lades, Guillaume Killian, Martin Gerfaud-Valentin, Mathieu Lemaire, Anne Chroboczek, Tomasz Liozon, Eric Gondran, Guillaume Sève, Pascal Monteil, Jacques Fauchais, Anne-Laure Ly, Kim Heang J Clin Med Article While the diagnosis of adult-onset Still’s disease (AOSD) involves the exclusion of differential diagnoses, the characteristics and value of 18F-Fluorodeoxyglucose (18F-FDG) Positron Emission Tomography coupled with CT (PET/CT) in the management of AOSD remain poorly known. Our retrospective study included patients from four centers, fulfilling Yamaguchi or Fautrel criteria, who underwent a PET/CT during an active AOSD. Thirty-five patients were included. At the time of PET/CT, the Yamaguchi criteria were met in 23 of 29 evaluable cases. PET/CT showed bone marrow (74.3%), lymph node (74.3%), and splenic (48.6%) FDG uptake. Despite arthralgia or arthritis in most patients, joints were rarely the sites of 18F-FDG accumulation. The spatial distribution of 18F-FDG uptake was nonspecific, and its intensity could be similar to malignant disease. Lymph node or bone marrow biopsy was performed after PET/CT in 20 patients (57.1%). The intensity of bone marrow; splenic and lymph node hypermetabolism appeared to be correlated with disease activity. Abnormal PET/CT in the cervical lymph nodes and age ≥ 60 years seemed to be predictive factors for monocyclic evolution. The clinical value of PET/CT is not in direct diagnosis; but as an aid in excluding differential diagnoses by searching for their scintigraphic features and guiding biopsy. MDPI 2021-06-04 /pmc/articles/PMC8200084/ /pubmed/34199846 http://dx.doi.org/10.3390/jcm10112489 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Brisset, Josselin
Jamilloux, Yvan
Dumonteil, Stephanie
Lades, Guillaume
Killian, Martin
Gerfaud-Valentin, Mathieu
Lemaire, Anne
Chroboczek, Tomasz
Liozon, Eric
Gondran, Guillaume
Sève, Pascal
Monteil, Jacques
Fauchais, Anne-Laure
Ly, Kim Heang
Characteristics and Clinical Value of 18F-FDG PET/CT in the Management of Adult-Onset Still’s Disease: 35 Cases
title Characteristics and Clinical Value of 18F-FDG PET/CT in the Management of Adult-Onset Still’s Disease: 35 Cases
title_full Characteristics and Clinical Value of 18F-FDG PET/CT in the Management of Adult-Onset Still’s Disease: 35 Cases
title_fullStr Characteristics and Clinical Value of 18F-FDG PET/CT in the Management of Adult-Onset Still’s Disease: 35 Cases
title_full_unstemmed Characteristics and Clinical Value of 18F-FDG PET/CT in the Management of Adult-Onset Still’s Disease: 35 Cases
title_short Characteristics and Clinical Value of 18F-FDG PET/CT in the Management of Adult-Onset Still’s Disease: 35 Cases
title_sort characteristics and clinical value of 18f-fdg pet/ct in the management of adult-onset still’s disease: 35 cases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200084/
https://www.ncbi.nlm.nih.gov/pubmed/34199846
http://dx.doi.org/10.3390/jcm10112489
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