18FDG PET scanning of benign and malignant musculoskeletal lesions

被引:67
作者
Feldman, F [1 ]
van Heertum, R
Manos, C
机构
[1] Columbia Univ, Coll Phys & Surg, New York, NY 10032 USA
[2] New York Presbyterian Hosp, New York, NY USA
关键词
(18)FDG PET; musculoskeletal lesions;
D O I
10.1007/s00256-003-0623-3
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: To describe the technique, applications and advantages of (18)FDG PET scanning in detection, analysis and management of musculoskeletal lesions. Design and patients: Forty-five patients (19 males, 26 females) aged 9 to 81 years had radiographs, routine radionuclide scans, CT and/or MRI of clinically suspected active benign or malignant musculoskeletal lesions. (18)FDG scans with a Siemens ECAT EXACT 921 dedicated PET unit (Knoxville, Tenn.) and FWH=6 mm. images acquired as a 5-6 bed examination (6 min emission and 4 min transmission) used OSEM iterative reconstruction with segmented transmission attenuation correction and a Gaussian filter (cutoff 6.7 mm). Region of interest (ROI) 3 x 3 pixel image analysis based on transverse whole body images (slice thickness 3.37 mm) generated Maximum Standard Uptake Values (Max SUV) with a cutoff of 2.0 used to distinguish benign and malignant lesions. Results: Thirty-nine studies were available for SUV ROI analysis. Overall sensitivity for differentiating malignant from benign osseous and non-osseous lesions was 91.7% (22/24), overall specificity was 100% (11/11) with an accuracy of 91.7%. All aggressive lesions had a Max SUV >2.0. Data separating benign from malignant lesions and aggressive from benign lesions were statistically significant (P<0.001) in both categories. There was no statistically significant difference in distinguishing aggressive from malignant lesions (P, ns). Conclusion: (18)FDG PET contributes unique information regarding metabolism of musculoskeletal lesions. By supplying a physiologic basis for more informed treatment and management, it influences prognosis and survival. Moreover, since residual, recurrent or metastatic tumors can be simultaneously documented on a single whole body scan, PET may theoretically prove to be cost-effective.
引用
收藏
页码:201 / 208
页数:8
相关论文
共 29 条
[11]   PET EVALUATION OF SOFT-TISSUE MASSES WITH F-18 FLUORO-2-DEOXY-D-GLUCOSE [J].
GRIFFETH, LK ;
DEHDASHTI, F ;
MCGUIRE, AH ;
MCGUIRE, DJ ;
PERRY, DJ ;
MOERLEIN, SM ;
SIEGEL, BA .
RADIOLOGY, 1992, 182 (01) :185-194
[12]   Chronic osteomyelitis: Detection with FDG PET and correlation with histopathologic findings [J].
Guhlmann, A ;
Brecht-Krauss, D ;
Sugar, G ;
Glatting, G ;
Kotzerke, J ;
Kinzl, L ;
Reske, SN .
RADIOLOGY, 1998, 206 (03) :749-754
[13]  
HAMBERG LM, 1994, J NUCL MED, V35, P1308
[14]  
KERN KA, 1988, J NUCL MED, V29, P181
[15]  
Kole AC, 1998, J NUCL MED, V39, P810
[16]   Detection of local recurrence of soft-tissue sarcoma with positron emission tomography using [F-18] fluorodeoxyglucose [J].
Kole, AC ;
Nieweg, OE ;
vanGinkel, RJ ;
Pruim, J ;
Hoekstra, HJ ;
Paans, AMJ ;
Vaalburg, W ;
Koops, HS .
ANNALS OF SURGICAL ONCOLOGY, 1997, 4 (01) :57-63
[17]  
KUBOTA R, 1992, J NUCL MED, V33, P1972
[18]   A PET study of 18FDG uptake in soft tissue masses [J].
Lodge, MA ;
Lucas, JD ;
Marsden, PK ;
Cronin, BF ;
O'Doherty, MJ ;
Smith, MA .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1999, 26 (01) :22-30
[19]   Evaluation of fluorodeoxyglucose positron emission tomography in the management of soft-tissue sarcomas [J].
Lucas, JD ;
O'Doherty, MJ ;
Wong, JCH ;
Bingham, JB ;
McKee, PH ;
Fletcher, CDM ;
Smith, MA .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1998, 80B (03) :441-447
[20]  
MATTHIAS HM, 2002, ANN SURG, V231, P380