Bone involvement in patients with lymphoma: the role of FDG-PET/CT

被引:99
作者
Schaefer, Niklaus G.
Strobel, Klaus
Taverna, Christian
Hany, Thomas F.
机构
[1] Univ Zurich Hosp, Dept Internal Med, Clin Med Oncol, CH-8091 Zurich, Switzerland
[2] Univ Zurich Hosp, Dept Nucl Med, CH-8091 Zurich, Switzerland
关键词
FDG-PET/CT; lymphoma; bone; bone marrow; biopsy;
D O I
10.1007/s00259-006-0238-8
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: To evaluate the diagnostic impact and clinical significance of FDG-avid bone lesions detected by FDG-PET/CT in patients with lymphoma. Methods: The study population comprised 50 consecutive patients (mean age 41.7 +/- 15.5 years; 27 female, 23 male; 41 staging, 9 restaging) with Hodgkin's disease (n=22) or aggressive non-Hodgkin's lymphoma (n=28) in whom FDG-avid bone lesions were detected by FDG-PET/CT. All patients had either direct biopsy of the FDG-avid bone lesion (n=18), standard bone marrow biopsy at the iliac crest (BMB; n=43) or both procedures (n=11). In 15 patients, additional MRI of the bone lesions was performed. All patients underwent FDG-PET/CT after the end of treatment. All CT images of FDG-PET/CT scans were analysed independently regarding morphological osseous changes and compared with FDG-PET results. Results: In the 50 patients, 193 FDG-avid lesions were found by PET/CT. The mean standardised uptake value was 6.26 (+/- 3.22). All direct bone biopsies (n=18) of the FDG-avid lesions proved the presence of lymphomatous infiltration. BMB (n=43) was positive in 12 patients (27.9%). In CT, 32 of 193 (16.6%) lesions were detected without the PET information. No additional morphological bone infiltration was detected on CT compared with FDG-PET. All morphological bone alterations on CT scans persisted after the end of therapy. Additional PET/CT information regarding uni- or multifocal bone involvement resulted in lymphoma upstaging in 21 (42%) patients compared with the combined information provided by CT and BMB. Conclusion: In patients with FDG-avid bone lesions, FDG-PET is superior to CT alone or in combination with unilateral BMB in detecting bone marrow involvement, leading to upstaging in a relevant proportion of patients.
引用
收藏
页码:60 / 67
页数:8
相关论文
共 27 条
[1]  
Buchmann I, 2000, RECENT RESULTS CANC, V156, P78
[2]   Fluorine-18 deoxyglucose positron emission tomography for the detection of bone metastases in patients with non-small cell lung cancer [J].
Bury, T ;
Barreto, A ;
Daenen, F ;
Barthelemy, N ;
Ghaye, B ;
Rigo, P .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1998, 25 (09) :1244-1247
[3]   Detection of lymphoma in bone marrow by whole-body positron emission tomography [J].
Carr, R ;
Barrington, SF ;
Madan, B ;
O'Doherty, MJ ;
Saunders, CAB ;
van der Walt, J ;
Timothy, AR .
BLOOD, 1998, 91 (09) :3340-3346
[4]   BONE-MARROW INVOLVEMENT BY NON-HODGKINS-LYMPHOMA - THE CLINICAL-SIGNIFICANCE OF MORPHOLOGICAL DISCORDANCE BETWEEN THE LYMPH-NODE AND BONE-MARROW [J].
CONLAN, MG ;
BAST, M ;
ARMITAGE, JO ;
WEISENBURGER, DD .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (07) :1163-1172
[5]  
FOUCAR K, 1982, CANCER, V49, P888, DOI 10.1002/1097-0142(19820301)49:5<888::AID-CNCR2820490512>3.0.CO
[6]  
2-K
[7]   BONE-MARROW EXAMINATION IN NEWLY-DIAGNOSED HODGKINS-DISEASE - CURRENT PRACTICE IN THE UNITED-KINGDOM [J].
HOWARD, MR ;
TAYLOR, PRA ;
LUCRAFT, HH ;
TAYLOR, MJ ;
PROCTOR, SJ .
BRITISH JOURNAL OF CANCER, 1995, 71 (01) :210-212
[8]   ESMO minimum clinical recommendations for diagnosis, treatment and follow-up of Hodgkin's disease [J].
Jost, LM ;
Stahel, RA .
ANNALS OF ONCOLOGY, 2005, 16 :54-55
[9]   ESMO Minimum Clinical Recommendations for diagnosis, treatment and follow-up of newly diagnosed large cell non-Hodgkin's lymphoma [J].
Jost, LM ;
Kloke, O ;
Stahel, RA .
ANNALS OF ONCOLOGY, 2005, 16 :58-59
[10]   PET-CT-guided percutaneous puncture of an infected cyst in autosomal dominant polycystic kidney disease: Case report [J].
Kaim, AH ;
Burger, C ;
Ganter, CC ;
Goerres, GW ;
Kamel, E ;
Weishaupt, D ;
Dizendorf, E ;
Schaffner, A ;
von Schulthess, GK .
RADIOLOGY, 2001, 221 (03) :818-821