Fluorine-18 labeled fluorodeoxyglucose positron emission tomography/computed tomography used in diagnosing connective tissue diseases in fever of unknown origin/inflammatory of unknown origin patients

被引:5
作者
Chen, Ziwei [1 ]
Li, Yuan [1 ]
Wang, Qian [1 ]
Weng, Shijia [1 ]
Zhou, Yunshan [2 ]
Zhu, Jihong [3 ]
机构
[1] Peking Univ Peoples Hosp, Dept Nucl Med, 11 Xizhimen South St, Beijing 100044, Peoples R China
[2] Peking Univ Peoples Hosp, Dept Rheumatol & Immunol, 11 Xizhimen South St, Beijing 100044, Peoples R China
[3] Peking Univ Peoples Hosp, Dept Emergency, 11 Xizhimen South St, Beijing 100044, Peoples R China
关键词
Connective tissue diseases; Fever of unknown origin; Fluorodeoxyglucose F18; Positron emission tomography computed tomography; SYSTEMIC-LUPUS-ERYTHEMATOSUS; RHEUMATOID-ARTHRITIS; FDG-PET/CT; F-18-FDG-PET/CT; INFLAMMATION; MALIGNANCY; COHORT;
D O I
10.1007/s10067-021-05965-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To explore the significance of Fluorine-18 labeled fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) in diagnosing connective tissue diseases (CTDs) in fever of unknown origin (FUO) or inflammation of unknown origin (IUO) patients. Methods Clinical and image data of 242 consecutive FUO/IUO patients who underwent PET/CT examination and eventually diagnosed CTDs were retrospectively analyzed, including distribution of diseases, clinical characteristics, and PET/CT imaging findings. The role of FDG PET/CT in differential diagnosis of CTDs was evaluated through clinical questionnaire survey. Results Patients diagnosed as CTDs accounted for 48.1% of FUO/IUO patients. Among them, adult-onset Still's disease was most frequently diagnosed. Other common diseases included systemic vasculitis, undifferentiated connective tissue disease, rheumatoid arthritis, idiopathic inflammatory myopathy, systemic lupus erythematosus, and polymyalgia rheumatica. On FDG PET/CT examination, 97.9% of the patients had positive findings. Inflammatory lesions were detected in 66.5% and non-specific abnormal uptakes were found in 31.4%. Detected lesions distributed consistently with corresponding susceptible organs and tissues in various diseases. Clinical questionnaire results shown that FDG PET/CT excluded malignant tumors, focal infections, or other typical CTDs in 45.5% of the patients; indicated important diagnostic clues or appropriate biopsy sites in 20.6% of patients; and directly suggested the diagnosis of a CTD in 33.1% of patients. Conclusion FDG PET/CT could reveal inflammatory lesions in organs and tissues that reflect the clinical characteristics in different CTDs, thus providing an objective evidence for differential diagnosis, classification, and treatment decision of these diseases.
引用
收藏
页码:839 / 846
页数:8
相关论文
共 37 条
  • [1] An International Cohort Study of Cancer in Systemic Lupus Erythematosus
    Bernatsky, S
    Boivin, JF
    Joseph, L
    Rajan, R
    Zoma, A
    Manzi, S
    Ginzler, E
    Urowitz, M
    Gladman, D
    Fortin, PR
    Petri, M
    Edworthy, S
    Barr, S
    Gordon, C
    Bae, SC
    Sibley, J
    Isenberg, D
    Rahman, A
    Aranow, C
    Dooley, MA
    Steinsson, K
    Nived, O
    Sturfelt, G
    Alarcón, G
    Senécal, JL
    Zummer, M
    Hanly, J
    Ensworth, S
    Pope, J
    El-Gabalawy, H
    McCarthy, T
    Pierre, YS
    Ramsey-Goldman, R
    Clarke, A
    [J]. ARTHRITIS AND RHEUMATISM, 2005, 52 (05): : 1481 - 1490
  • [2] Fever of unknown origin: large vessel vasculitis diagnosed by PET/CT
    Bosnic, Dubravka
    Baresic, Marko
    Padjen, Ivan
    Balenovic, Antonija
    Zarkovic, Kamelija
    Anic, Branimir
    [J]. RHEUMATOLOGY INTERNATIONAL, 2013, 33 (09) : 2417 - 2421
  • [3] Morbidity and mortality in systemic lupus erythematosus during a 10-year period -: A comparison of early and late manifestations in a cohort of 1,000 patients
    Cervera, R
    Khamashta, MA
    Font, J
    Sebastiani, GD
    Gil, A
    Lavilla, P
    Mejía, JC
    Aydintug, AC
    Chwalinska-Sadowska, H
    de Ramón, E
    Fernández-Nebro, A
    Galeazzi, M
    Valen, M
    Mathieu, A
    Houssiau, FD
    Caro, N
    Alba, P
    Ramos-Casals, M
    Ingelmo, M
    Hughes, GRV
    [J]. MEDICINE, 2003, 82 (05) : 299 - 308
  • [4] Fever of unknown origin: Focused diagnostic approach based on clinical clues from the history, physical examination, and laboratory tests
    Cunha, Burke A.
    [J]. INFECTIOUS DISEASE CLINICS OF NORTH AMERICA, 2007, 21 (04) : 1137 - +
  • [5] Malignancy and rheumatoid arthritis: Epidemiology, risk factors and management
    De Cock, Diederik
    Hyrich, Kimme
    [J]. BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2018, 32 (06): : 869 - 886
  • [6] Lung Infections in Systemic Rheumatic Disease: Focus on Opportunistic Infections
    Di Franco, Manuela
    Lucchino, Bruno
    Spaziante, Martina
    Iannuccelli, Cristina
    Valesini, Guido
    Iaiani, Giancarlo
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (02)
  • [7] Frequency of infection in patients with rheumatoid arthritis compared with controls - A population-based study
    Doran, MF
    Crowson, CS
    Pond, GR
    O'Fallon, WM
    Gabriel, SE
    [J]. ARTHRITIS AND RHEUMATISM, 2002, 46 (09): : 2287 - 2293
  • [8] SLE diagnosis and treatment: When early is early
    Doria, Andrea
    Zen, Margherita
    Canova, Mariagrazia
    Bettio, Silvano
    Bassi, Nicola
    Nalotto, Linda
    Rampudda, Mariaelisa
    Ghirardello, Anna
    Iaccarino, Luca
    [J]. AUTOIMMUNITY REVIEWS, 2010, 10 (01) : 55 - 60
  • [9] The Diagnostic Role of FDG PET/CT in Patients with Fever of Unknown Origin
    Ergul, Nurhan
    Halac, Metin
    Cermik, Tevfik F.
    Ozaras, Resat
    Sager, Sait
    Onsel, Cetin
    Uslu, Ilhami
    [J]. MOLECULAR IMAGING AND RADIONUCLIDE THERAPY, 2011, 20 (01) : 19 - 25
  • [10] Fever of unknown origin (FUO): which are the factors influencing the final diagnosis? A 2005-2015 systematic review
    Fusco, Francesco Maria
    Pisapia, Raffaella
    Nardiello, Salvatore
    Cicala, Stefano Domenico
    Gaeta, Giovanni Battista
    Brancaccio, Giuseppina
    [J]. BMC INFECTIOUS DISEASES, 2019, 19 (1)