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

18F-FDG PET/CT adult-onset Still’s disease

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
04 Jun 2021
Historique:
received: 16 04 2021
revised: 31 05 2021
accepted: 02 06 2021
entrez: 2 7 2021
pubmed: 3 7 2021
medline: 3 7 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 34199846
pii: jcm10112489
doi: 10.3390/jcm10112489
pmc: PMC8200084
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Josselin Brisset (J)

Service de Médecine Interne, CHU Dupuytren, 87000 Limoges, France.
Service de Maladies Infectieuses et Tropicales, CHU Dupuytren, 87000 Limoges, France.

Yvan Jamilloux (Y)

Service de Médecine Interne, Hôpital de la Croix-Rousse, 69004 Lyon, France.

Stephanie Dumonteil (S)

Service de Médecine Interne, CHU Dupuytren, 87000 Limoges, France.

Guillaume Lades (G)

Service de Médecine Nucléaire, CHU Dupuytren, 87000 Limoges, France.

Martin Killian (M)

Service de Médecine Interne, CHU Saint-Etienne, 42055 Saint-Etienne, France.

Mathieu Gerfaud-Valentin (M)

Service de Médecine Interne, Hôpital de la Croix-Rousse, 69004 Lyon, France.

Anne Lemaire (A)

Service de Médecine Interne, Centre Hospitalier Alpes-Léman, 74130 Contamine-sur-Arve, France.

Tomasz Chroboczek (T)

Service de Maladies Infectieuses, Centre Hospitalier Alpes-Léman, 74130 Contamine-sur-Arve, France.

Eric Liozon (E)

Service de Médecine Interne, CHU Dupuytren, 87000 Limoges, France.

Guillaume Gondran (G)

Service de Médecine Interne, CHU Dupuytren, 87000 Limoges, France.

Pascal Sève (P)

Service de Médecine Interne, Hôpital de la Croix-Rousse, 69004 Lyon, France.

Jacques Monteil (J)

Service de Médecine Nucléaire, CHU Dupuytren, 87000 Limoges, France.

Anne-Laure Fauchais (AL)

Service de Médecine Interne, CHU Dupuytren, 87000 Limoges, France.

Kim Heang Ly (KH)

Service de Médecine Interne, CHU Dupuytren, 87000 Limoges, France.

Classifications MeSH