18-Fluorodeoxyglucose-Positron Emission Tomography (FDG-PET) Evaluation of Nodular Lesions in Patients With Neurofibromatosis Type 1 and Plexiform Neurofibromas (PN) or Malignant Peripheral Nerve Sheath Tumors (MPNST)

被引:45
作者
Meany, Holly [1 ,2 ]
Dombi, Eva [2 ]
Reynolds, James [3 ]
Whatley, Millie [3 ]
Kurwa, Ambereen [2 ]
Tsokos, Maria [4 ]
Salzer, Wanda [2 ]
Gillespie, Andrea [2 ]
Baldwin, Andrea [2 ]
Derdak, Joanne [2 ]
Widemann, Brigitte [2 ]
机构
[1] Childrens Natl Med Ctr, Dept Hematol Oncol, Washington, DC 20010 USA
[2] NCI, Pharmacol & Expt Therapeut Sect, Pediat Oncol Branch, Ctr Canc Res,NIH, Bethesda, MD 20892 USA
[3] NCI, Dept Nucl Med, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[4] NCI, Pathol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
关键词
18-fluorodeoxyglucose-positron emission tomography (FDG-PET); malignant peripheral nerve sheath tumors (MPNST); neurofibromatosis; plexiform neurofibromas (PN); MRI;
D O I
10.1002/pbc.24212
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Individuals with Neurofibromatosis type 1 (NF1) are at risk for developing malignant peripheral nerve sheath tumors (MPNST), which frequently arise in preexisting plexiform neurofibromas (PN). Magnetic resonance imaging (MRI) with volumetric analysis and 18-fluorodeoxyglucose-positron emission tomography (FDG-PET) were utilized to monitor symptomatic nodular lesions. Procedure. Patients with NF1 and PN on a NCI natural history trial were monitored for total body tumor volume (TTV) using volumetric MRI. FDG-PET was performed in individuals with a nodular well-demarcated lesion >= 3 cm if they were growing, painful, or there was a prior history of MPNST (target lesions). Asymptomatic nodular lesions were evaluated as non-target lesions. Results. Fifteen patients (8m, 7f) median age of 18.3 years (range, 10-45 years) had a single target and non-target (n = 46) nodular lesions identified on MRI. Target lesions arose within (n = 8) or outside (n = 3) a PN, and all but 1 had increased FDG uptake. FDG uptake was increased in non-target lesions but to a lesser degree. FDG uptake in the surrounding PN was low, similar to background activity. Pathologic evaluation performed in 11 patients demonstrated neurofibroma (n = 6), atypical neurofibroma (n = 2) and malignancy (n = 3). Conclusions. Nodular target lesions identified on MRI in individuals with NF1 and PN demonstrate increased FDG uptake similar to MPNST, but may be benign on biopsy. Nodular target lesions may be at greater risk for malignant transformation, but their biologic and clinical behavior has not been well studied. Careful longitudinal evaluation will be required to better understand the malignant potential of these lesions. Pediatr Blood Cancer 2013; 60: 59-64. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:59 / 64
页数:6
相关论文
共 28 条
[1]   Combined PET/MRI: a new dimension in whole-body oncology imaging? [J].
Antoch, Gerald ;
Bockisch, Andreas .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2009, 36 :113-120
[2]   Atypical Neurofibromas in Neurofibromatosis Type 1 are Premalignant Tumors [J].
Beert, Eline ;
Brems, Hilde ;
Daniels, Bruno ;
De Wever, Ivo ;
Van Calenbergh, Frank ;
Schoenaers, Joseph ;
Debiec-Rychter, Maria ;
Gevaert, Olivier ;
De Raedt, Thomas ;
Van den Bruel, Annick ;
de Ravel, Thomy ;
Cichowski, Karen ;
Kluwe, Lan ;
Mautner, Victor ;
Sciot, Raf ;
Legius, Eric .
GENES CHROMOSOMES & CANCER, 2011, 50 (12) :1021-1032
[3]   Utility of 18 FDG positon emission tomography in detection of sarcomatous transformation in neurofibromatosis type I [J].
Bensaid, B. ;
Giammarile, F. ;
Mognetti, T. ;
Galoisy-Guibal, L. ;
Pinson, S. ;
Drouet, A. ;
Combemale, P. .
ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE, 2007, 134 (10) :735-741
[4]  
Benz MR, CANCER AM CANCER SOC, V116, P451
[5]   Value of PET in the assessment of patients with neurofibromatosis type I [J].
Bredella, Miriam A. ;
Torriani, Martin ;
Hornicek, Francis ;
Ouellette, Hugue A. ;
Palmer, William E. ;
Williams, Ziv ;
Fishman, Allan J. ;
Plotkin, Scott R. .
AMERICAN JOURNAL OF ROENTGENOLOGY, 2007, 189 (04) :928-935
[6]   Prognostic relevance of FDG PET in patients with neurofibromatosis type-1 and malignant peripheral nerve sheath tumours [J].
Brenner, W ;
Friedrich, RE ;
Gawad, KA ;
Hagel, C ;
von Deimling, A ;
de Wit, M ;
Buchert, R ;
Clausen, M ;
Mautner, VF .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2006, 33 (04) :428-432
[7]   Pediatric malignant peripheral nerve sheath tumor: The Italian and German soft tissue sarcoma cooperative group [J].
Carli, M ;
Ferrari, A ;
Mattke, A ;
Zanetti, I ;
Casanova, M ;
Bisogno, G ;
Cecchetto, G ;
Alaggio, R ;
De Sio, L ;
Koscielniak, E ;
Sotti, G ;
Treuner, J .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (33) :8422-8430
[8]   MALIGNANT PERIPHERAL-NERVE SHEATH TUMORS - THE ST-JUDE-CHILDRENS-RESEARCH-HOSPITAL EXPERIENCE [J].
DECOU, JM ;
RAO, BN ;
PARHAM, DM ;
LOBE, TE ;
BOWMAN, L ;
PAPPO, AS ;
FONTANESI, J .
ANNALS OF SURGICAL ONCOLOGY, 1995, 2 (06) :524-529
[9]   NF1 plexiform neurofibroma growth rate by volumetric MRI - Relationship to age and body weight [J].
Dombi, E. ;
Solomon, J. ;
Gillespie, A. J. ;
Fox, E. ;
Balis, F. M. ;
Patronas, N. ;
Korf, B. R. ;
Babovic-Vuksanovic, D. ;
Packer, R. J. ;
Belasco, J. ;
Goldman, S. ;
Jakacki, R. ;
Kieran, M. ;
Steinberg, S. M. ;
Widemann, B. C. .
NEUROLOGY, 2007, 68 (09) :643-647
[10]  
DUCATMAN BS, 1986, CANCER-AM CANCER SOC, V57, P2006, DOI 10.1002/1097-0142(19860515)57:10<2006::AID-CNCR2820571022>3.0.CO