The utility of fluorine-18-fluorodeoxyglucose positron emission tomography in the diagnosis and monitoring of large vessel vasculitis: A South Australian retrospective audit.


Journal

International journal of rheumatic diseases
ISSN: 1756-185X
Titre abrégé: Int J Rheum Dis
Pays: England
ID NLM: 101474930

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 14 02 2018
revised: 12 03 2019
accepted: 09 05 2019
pubmed: 19 6 2019
medline: 30 1 2020
entrez: 19 6 2019
Statut: ppublish

Résumé

To investigate the utility of fluorine-18-labelled deoxyglucose positron emission tomography (FDG-PET) in routine clinical practice to diagnose and monitor disease activity and treatment response in large vessel vasculitis in a South Australian cohort. We performed a retrospective clinical audit of adult patients who received a FDG-PET at a tertiary referral center between August 2010 and August 2015, where the term "vasculitis" appeared in either the request or report. A total of 45 patients met the inclusion criteria. Nine patients (20%) had a positive FDG-PET for large vessel vasculitis. FDG-PET was positive in 3/6 (50%) patients who met the American College of Rheumatology (ACR) criteria for giant cell arteritis or Takayasu's arteritis (TA) on retrospective review. A positive FDG-PET for large vessel inflammation assisted the primary clinician in making the diagnosis of unclassified large vessel vasculitis in six patients. Four of the seven patients who had more than one scan for large vessel vasculitis demonstrated normalized FDG uptake on subsequent scans after a period on glucocorticoid treatment. The remaining three patients persisted in having increased FDG uptake on FDG-PET imaging while on active treatment. Fluorine-18-labelled deoxyglucose positron emission tomography has a role in the diagnosis of large vessel vasculitis, particularly in patients with a high suspicion of active large vessel vasculitis who do not meet the ACR criteria. FDG-PET may have a role in monitoring disease activity in selected patients with large vessel vasculitis especially in identifying occult sites of large vessel inflammation or to titrate prednisolone therapy.

Identifiants

pubmed: 31211510
doi: 10.1111/1756-185X.13617
doi:

Substances chimiques

Glucocorticoids 0
Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1378-1382

Informations de copyright

© 2019 Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd.

Auteurs

Ai Duyen Nguyen (AD)

Department of Medicine, Royal Adelaide Hospital, Adelaide, South Australia, Australia.

Thomas Crowhurst (T)

Department of Thoracic Medicine, Royal Adelaide Hospital, Adelaide, South Australia, Australia.

Susan Lester (S)

Rheumatology Unit, The Queen Elizabeth Hospital, Woodville, South Australia, Australia.
Rheumatology Unit, Royal Adelaide Hospital, Adelaide, South Australia, Australia.

Rachael Dobson (R)

Department of Nuclear Medicine, Royal Adelaide Hospital, Adelaide, South Australia, Australia.

Dylan Bartholomeusz (D)

Department of Nuclear Medicine, Royal Adelaide Hospital, Adelaide, South Australia, Australia.

Catherine Hill (C)

Rheumatology Unit, The Queen Elizabeth Hospital, Woodville, South Australia, Australia.
Rheumatology Unit, Royal Adelaide Hospital, Adelaide, South Australia, Australia.

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Classifications MeSH