PET/MRI in large-vessel vasculitis: clinical value for diagnosis and assessment of disease activity.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
27 08 2019
Historique:
received: 20 02 2019
accepted: 23 07 2019
entrez: 29 8 2019
pubmed: 29 8 2019
medline: 30 10 2020
Statut: epublish

Résumé

Diagnosis of large vessel vasculitis (LVV) and evaluation of its inflammatory activity can be challenging. Our aim was to investigate the value of hybrid positron-emission tomography/magnetic resonance imaging (PET/MRI) in LVV. All consecutive patients with LVV from the Department of Internal Medicine who underwent PET/MRI were included. Three PET/MRI patterns were defined: (i) "inflammatory," with positive PET (>liver uptake) and abnormal MRI (stenosis and/or wall thickening); (ii) "fibrous", negative PET (≤liver uptake) and abnormal MRI; and (iii) "normal". Thirteen patients (10 female; median age: 67-years [range: 23-87]) underwent 18 PET/MRI scans. PET/MRI was performed at diagnosis (n = 4), at relapse (n = 7), or during remission (n = 7). Among the 18 scans, eight (44%) showed an inflammatory pattern and three (17%) a fibrous pattern; the other seven were normal. The distribution of the three patterns did not differ between patients with Takayasu arteritis (TA, n = 10 scans) and those with giant cell arteritis (GCA, n = 8 scans). PET/MRI findings were normal in 2/10 (20%) TA scans vs. 5/8 (62%) GCA scans (p = 0.3). Median SUV

Identifiants

pubmed: 31455785
doi: 10.1038/s41598-019-48709-w
pii: 10.1038/s41598-019-48709-w
pmc: PMC6711961
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

12388

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Auteurs

Charlotte Laurent (C)

AP-HP, Sorbonne Université, Hôpital Saint-Antoine, Service de Médecine Interne and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), F-75012, Paris, France.

Laure Ricard (L)

AP-HP, Sorbonne Université, Hôpital Saint-Antoine, Service de Médecine Interne and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), F-75012, Paris, France.

Olivier Fain (O)

AP-HP, Sorbonne Université, Hôpital Saint-Antoine, Service de Médecine Interne and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), F-75012, Paris, France.

Irene Buvat (I)

IMIV, CEA, INSERM, Université Paris Sud, CNRS, Université Paris Saclay, Orsay, France.

Amir Adedjouma (A)

AP-HP, Sorbonne Université, Hôpital Saint-Antoine, Service de Médecine Interne and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), F-75012, Paris, France.

Michael Soussan (M)

IMIV, CEA, INSERM, Université Paris Sud, CNRS, Université Paris Saclay, Orsay, France.
APHP, Hôpital Avicenne, Service de Médecine Nucléaire, Paris 13 University, Bobigny, France.

Arsène Mekinian (A)

AP-HP, Sorbonne Université, Hôpital Saint-Antoine, Service de Médecine Interne and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), F-75012, Paris, France. arsene.mekinian@aphp.fr.

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Classifications MeSH