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63. Yates RW, Marsden PK, Badawi RD, et al. Evaluation of myocardial per- fusion using positron emission tomography in infants following a neona- tal arterial switch operation. Pediatr Cardiol 2000;21 (2):111–118. 64.Hauser M, Bengel FM, Kuhn A, et al. Myocardial perfusion and coronary flow reserve assessed by positron emission tomography in patients after Fontan-like operations. Ped iatr Cardiol 2003;24(4):386–392. 65.Hauser M, Bengel FM, Kuhn A, et al. Myocardial blood flow and flow reserve after coronary reimplantation in patients. Circulation 2001;103: 1875–1880. 66. Ric kers C, Sasse K, Buchert R, et al. Myocardial viability assessed by positron emission tomography in infants and children after the arterial switch operation and suspected infarction. J Am Coll Cardiol 2000; 36(5):1676–1683. 67. Hwang B, Liu RS, Chu LS, et al. Positron emission tomography for the assessment of myocardial viability in Kawasaki disease using different therapies. Nucl Med Commun 2000;21(7):631–636. 68. Litvinova I, Litvinov M, Loeonteva I, et al. PET for diagnosis of mito- chondrial cardiomyopathy in children. Clin Positron Imaging 2000;3(4): 172. 69. Skehan SJ, Issenman R, Mernagh J, et al. 18F-fluorodeoxyglucose positron tomography in diagnosis of pediatric inflammatory bowel disease. Lancet 1999;354:836–837. 70. Gungor T, Engel-Bicik I, Eich G, et al. Diagnostic a nd therapeutic impact of whole body positron emission tomography using fluorine-18-fluoro-2- deoxy-D-glucose in children with chronic granulomatous disease. Arch Dis Child 2001;85:341–345. 71. Muller AE, Kluge R, Biesold M, et al. Whole body positron emission tomography detected occult infectious foci in a child with acute myeloid leukaemia. Med Pediatr Oncol 2002;38:58–59. 72.Tomas MB, Tronc o GG, Karayalcin G, et al. FDG uptake in infectious mononucleosis. Clin Positron Imaging 2000;3:176. 73. Franzius C, Biermann M, Hulskamp G, et al. Therapy monitoring in aspergillosis using F-18 FDG positron emission tomography. Clin Nucl Med 2001;26:232–233. 74. Richard JC, Chen DL, Ferkol T, et al. Molecular imaging for pediatric lung diseases. Pediatr Pulmonol 2004;37(4):286–296. 75. Jones H, Sriskandan S, Peters A, et al. Dissociation of neutrophil emigra - tion and metabolic activity in lobar pneumonia and bronchiectasis. Eur Respir J 1997;10:795–803. 76. Jones HASJ, Krausz T, Boobis AR, et al. Pulmonary fibrosis correlates with duration of tissue neutrophil activation. Am J Respir Crit Care Med 1998;158:620–628. 77. Jones HA, Clark RJ, Rhodes CG, et al. In vivo measurement of neutrophil activity in experimental lung inflammation. Am J Respir Crit Care Med 1994;149:1635–1639. 78. Kapucu L, Meltzer C, Townsend DV, et al. Fluorine-18–fluorodeoxyglu- cose uptake in pneumonia. J Nucl Med 1998;39:1267–1269. 79. Jones H, Marino P, Shakur B, et al. In vivo assessment of lung inflamma- tory cell activity in patients with COPD and asthma. Eur Respir J 2003;21: 567–573. 80.Pantin CF, Valind SO, Sweatman M, et al. Measures of the inflammatory response in cryptogenic fibrosing alveolitis. Am Rev Respir Dis 1988;1 38: 1234–1241. F. Ponzo and M. Charron 517 81.Taylor I, Hill A, Hayes M, et al. Imaging allergen-invoked airway inflam- mation in atopic asthma with (18F)-fluorodeoxyglucose and positron emission tomography. Lancet 1996;347:937–940. 82. Kirpalani H, Abubakar K, Nahmias C, et al. (18F)fluorodeoxyglucose uptake in neonatal acute lung injury measured by positron emission tomography. Pediatr Res 1997;41:892–896. 83. FitzSimmons S. The changing epidemiology of cystic fibrosis. J Pediatr 1993;122:1–9. 84. Richard JC, Chen DL, Ferkol T, et al. Molecular imaging for pediatric lung diseases. Pediatr Pulmonol 2004;37(4):286–296. 85.Konstan M, Hilliard K, Norvell T, et al. Bronchoalveolar lavage fin dings in cystic fibrosis patients with stable, clinically mild lung disease suggest ongoing infection and inflammation. Am J Respir Crit Care Med 1994; 150:448–454. 86.Chen D,Wilson K, Mintun M, et al. Evaluating pulmonary inflamma- tion with 18F-fluorodeoxyglucose and positron emission tomography in patients with cystic fibrosis. Am J Respir Crit Care Med 2003;167: 323. 87. Chen DL, Pittman JE, Rosembluth DB. Evaluating pulmonary inflamma- tion with 18F-fluorodeoxyglucose and positron emission tomography in patients with cystic fibrosis Presented at the 51 st annual meeting of the Society of Nuclear Medicine 2004:534. 88. Brudin LH, Valind SO, Rhodes CG, et al. Fluorine-18 deoxyglucose uptake in sarcoidosis measured with positron emission tomography. Eur J Nucl Med 1994;21:297–305. 89. Weinblatt ME, Zanzi I, Belakhlef A, et al. False-positive FDG-PET imaging of the thymus of a child with Hodgkin’s disease. J Nucl Med 1997;38: 888–890. 90.Patel PM, Alibazoglu H, Ali A, et al. Normal thymic uptake of FD G on PET imaging. Clin Nucl Med 1996;21:772–775. 91. Delbeke D. Oncological applications of FDG-PET imaging: colorectal cancer, lymphoma, and melanoma. J Nucl Med 1999;40:591–603. 92. Yeung HW, Grewal RK, Gonen M, et al. Patterns of (18)F-FDG uptake in adipose tissue and muscle: a potential source of false-positives for PET. J Nucl Med 2003;44(11):1789–1796. 93. Minotti AJ, Shah L, Keller K. Positron emission to mography/computed tomography fusion imaging in brown adipose tissue. Clin Nucl Med 2004;29(1):5–11. 94.Hany TF, Gharehpapagh E, Kamel EM, et al. Brown adipose tissue: a factor to consider in symmetrical tracer uptake in the neck and upper chest region. Eur J Nucl Med Mol Imaging 2002;29:1393–1398. 95.Cohade C, Osman M, Pannu HK, et al. Uptake in supraclavicular area fat (“USA-Fat”): description on 18F-FDG-PET/CT. J Nucl Med 2003;44: 170–176. 96.Tatsumi M, Engles JM, Ishimori T, et al. Intense (18)F-FDG uptake in brown fat can be reduced pharmacologically. J Nucl Med 2004;45(7):1189– 1193. 97. Gelfand MJ, O’Hara SM, Curtwright LA, MacLean JR. Pre-medication to limit brown adipose tissue uptake of (F-18) FDG on PET body imaging. Pediatr Radiol 2005;4(suppl 1):S54. 98. Bar-Sever Z, Keidar Z, Ben Arush M, et al. The incremental value of PET/CT over stand-alone PET in pediatric malignancies. Presented at the 51 st annual meeting of the Society of Nuclear Medicine 2004: 379. 518Chapter 28 Current Research Efforts 99. Shaefer N, et al. Non Hodgkin’s lymphoma and Hodgkin’s disease: coreg- istrated FDG PET and CT at staging and restaging. Do we need contrast enhanced CT? Radiology 2004;232:823–829. 100. Antoch G, Freudenberg LS, Beyer T, et al. To enhance or not to enhance? 18FDG and CT contrast agent in dual modality 18FDG PET/CT. J Nucl Med 2004;45:56S–65S. 101. Antoch G, Freudenberg LS, Stattaus J, et al. Whole-body positron emis- sion tomography-CT: optimized CT using oral and IV contrast materials. AJR 2002;179:1555–1560. 102.Tatsumi M, Miller JH, Whal RL. (F-18) FDG-PET/CT in pediatric lym- phoma: comparis on with contrast enhanced CT. Presented at the 51 st annual meeting of the Society of Nuclear Medicine 2004:1107. 103. Sugawara Y, Fisher SJ, Zasadny KR, et al. Preclinical and clinical studies of bone marrow uptake of fluorine-1–fluorodeoxyglucose with o r without granulocyte colony-stimulating factor during chemotherapy. J Clin Oncol 1998;16:173–180. 104.Hollinger EF, Alibazoglu H, Ali A, et al. Hematopoietic cytokine- mediated FDG uptake simulates the appearance of diffuse metastatic disease on whole-body PET imaging. Clin Nucl Med 1998;23:93–98. 105. Brink I, Reinhardt MJ, Hoegerle S, et al. Increased metabolic activity in the thymus gland stu died with 18F-FDG-PET: age dependency and fre- quency after chemotherapy. J Nucl Med 2001;42:591–595. 106. Bujenovic S, Mannting F, Chakrabarti R, et al. Artifactual 2-deoxy-2- ((18)F)fluoro-D-deoxyglucose localization surrounding metallic objects in a PET/CT scanner using CT-based attenuation correction. Mol Imaging Biol 2003;5:20–22. 107. Valk PE, Budinger TF, Levin VA, et al. PET of malignant cerebral tumors after interstitial brachytherapy. Demonstration of metabolic activity and correlation with clinical outcome. J Neurosurg 1988;69:830–838. 108. Di Chiro G, Oldfield E, Wright DC, et al. Cerebral necrosis after radio- therapy and/or intraarterial chemotherapy for brain tumors: PET and neuropathologic studies. AJR 1988;150:189–197. 109.Glantz MJ, Hoffman JM, Coleman RE, et al. Identification of early recur- rence of primary central nervous system tumors by (18F)fluorodeoxyglu- cose positron emission tomograph. Ann Neurol 1991;29:347–355. 110. Bruggers CS, Friedman HS, Fuller GN, et al. Comparison of serial PET and MRI scans in a pediatric patient with a brainstem glioma. Med Pediatr Oncol 1993;21(4):301–306. 111.Molloy PT, Belasco J, Ngo K, et al. The ro le of FDG-PET imaging in the clinical management of pediatric brain tumors. J Nucl Med 1999;40: 129P. 112.Holthof VA, Herholz K, Berthold F, et al. In vivo metabolism of childhood posterior fossa tumors and primitive neuroectodermal tumors before and after treatment. Cancer 1993;1394–1403. 113. Hoffman JM, Hanson MW, Friedman HS, et al. FDGPET in pediatric pos- terior fossa brain tumors. J Comput Assist Tomogr 1992;16:62–68. 114 . Pirotte B, Goldman S, Salzberg S, et al. Combined positron emission tomography and magnetic resonance imaging for the planning of stereo- tactic brain biopsies in children: experience in 9 cases. Pediatr Neurosurg 2003;38(3):146–155. 115.Kaplan AM, Bandy DJ, Manwaring KH, et al. Functional brain mapping using positron emission tomography scanning in preoperative neuro- surgical planning for pediatric brain tumors. J Neurosurg 1999;91:797– 803. F. Ponzo and M. Charron 519 116.Molloy PT, Defeo R, Hunter J, et al. Excellent correlation of FDG-PET imaging with clinical outcome in patients with neurofibromatosis type I and low grade astrocytomas. J Nucl Med 1999;40:129P. 117. Jadvar H, Alavi A, Mavi A, Shulkin BL. PET imaging in pediatric diseases. Radiol Clin North Am 2005;43:135–152. 118. Inoue T, Shibasaki T, Oriuchi N, et al. 18F-alpha-methyl tyrosine PET studies in patients with brain tumors. J Nucl Med 1999;40:399–405. 119. Utriainen M, Metsahonkala L, Salmi TT, et al. Metabolic characterization of childhood brain tumors: comparison of 18F-fluorodeoxyglucose and 11C-methionine positron emission tomography. C ancer 2002;95:1376– 1386. 120. Vander Borght T, Pauwels S, Lambotte L, et al. Brain tumor imaging with PET and 2-(carbon-11)thymidine. J Nucl Med 1994;35:974–982. 121. Weckesser M, Langen KJ, Rickert CH, et al. Initial experiences with O-(2- (18F)-fluorethyl)-L-tyrosine PET in the evaluation of primary bone tumors. Presented at the 51 st annual meeting of the Society of Nuclear Medicine Meeting 2004:513. 122. Philip I, Shun A, McCowage G, Howman-Giles R. Positron emission tomography in recurrent hepatoblastoma. Pediatr Surg Int 2005;21(5):341– 345. 123. Barringt on SF, Carr R. Staging of Burkitt’s lymphoma and response to treatment monitored by PET scanning. Clin Oncol 1995;7:334–335. 124. Bangerter M, Moog F, Buchmann I, et al. Whole-body 2–(18F)-fluoro-2- deoxy-D-glucose positron emission tomography (FDG-PET) for accurate staging of Hodgkin’s disease. Ann Oncol 1998;9:1117–1122. 125. Jerusalem G, Warland V, Najjar F, et al. Whole-body 18F-FDG-PET for the evaluation of patients with Hodgkin’s disease and non-Hodgkin’s lym- phoma. Nucl Med Commun 1999;20:13–20. 126. Leskinen-Kallio S, Ruotsalainen U, Nagren K, et al. Uptake of carbon-11- methionine an d fluorodeoxyglucose in non-Hodgkin’s lymphoma: a PET study. J Nucl Med 1991;32:1211–1218. 127. Moog F, Bangerter M, Kotzerke J, et al. 18-F-fluorodeoxyglucose positron emission tomography as a new approach to detect lymphomatous bone marrow. J Clin Oncol 1998;16:603–609. 128. Moog F, Bangerter M, Diederichs CG, et al. Extranodal malignant lym- phoma: detection with FDG-PET versus CT. Radiology 1998;206:475– 481. 129.Moog F, Bangerter M, Diederichs CG, et al. Lymphoma: role of whole- body 2-deoxy-2-(F-18)fluoro-D-glucose (FDG) PET in nodal staging. Radiology 1997;203:795–800. 130.Okada J, Yoshikawa K, Imazeki K, et al. The use of FDG-PET in the detec- tion and management of malignant lymphoma: correlation of uptake with prognosis. J Nucl Med 1991;32:686–691. 131.Okada J, Yoshikawa K, Itami M, et al. Positron emission tomography using fluorine-18–fluorodeoxyglucose in malignant lymphoma: a com- parison with proliferative activity. J Nucl Med 1992;33:325–329. 132. Rodriguez M, Rehn S, Ahlstrom H, et al. Predicting malignancy grade with PET in non-Hodgkin’s lymphoma. J Nucl Med 1995;36:1790–1796. 133. Newman JS, Francis IR, Kaminski MS, et al. Imaging of lymphoma with PET with 2-(F-18)-fluoro-2-deoxy-D-glucose: correlation with CT. Radiol- ogy 1994;190:111–116. 134. de Wit M, Bumann D, Beyer W, et al. Whole-body positron emission tomography (PET) for diagnosis of residual mass in patients with lym- phoma. Ann Oncol 1997;8(suppl 1):57–60. 520Chapter 28 Current Research Efforts 135.Cremerius U, Fabry U, Neuerburg J, et al. Positron emission tomography with 18-F-FDG to detect residual disease after therapy for malignant lym- phoma. Nucl Med Commun 1998;19:1055–1063. 136.Ho h CK, Glaspy J, Rosen P, et al. Whole-body FDGPET imaging for staging of Hodgkin’s disease and lymphoma. J Nucl Med 1997;38:343– 348. 137. Romer W, Hanauske AR, Ziegler S, et al. Positron emission tomography in non-Hodgkin’s lymphoma: assessment of chemotherapy with fluo- rodeoxyglucose. Blood 1998;91:4464–4471. 138. Stumpe KD, Urbinelli M, Steinert HC, et al. Whole-body positron emis- sio n tomography using fluorodeoxyglucose for staging of lymphoma: effectiveness and comparison with computed tomography. Eur J Nucl Med 1998;25:721–728. 139. Lapela M, Leskinen S, Minn HR, et al. Increased glucose metabolism in untreated non-Hodgkin’s lymphoma: a study with positron emission tomography and fluorine-18-fluorodeoxyglucose. Blood 1995;86:3522– 3527. 140.Carr R, Barrington SF, Madan B, et al. Detection of lymphoma in bone marrow by whole-body positron emission tomography. Blood 1998;91: 3340–3346. 141. Segall GM. FDG-PET imaging in patients with lymphoma: a clinical per- specti ve. J Nucl Med 2001;42(4):609–610. 142.Moody R, Shulkin B, Yanik G, et al. PET FDG imaging in pediatric lym- phomas. J Nucl Med 2001;42(5 suppl):39P. 143. Kostakoglu L, Leonard JP, C oleman M, et al. Comparison of FDG-PET and Ga-67 SPECT in the staging of lymphoma. Cancer 2002;94(4):879– 888. 144. Lin PC, Chu J, Pocock N. F-18 fluorodeoxyglucose imaging with coinci- dence dual-head gamma camera (hybrid FDG-PET) for staging of lym- phoma: comparison with Ga-67 scintigraphy. J Nucl Med 2000;41(5 suppl): 118P. 145.Tomas MB, Manalili E, Leonidas JC, et al. F-18 FDG imaging of lymphoma in children using a hybrid pet system: comparison with Ga-67. J Nucl Med 2000;41(5 suppl):96P. 146.Tatsumi M, Kitayama H, Sugahara H, et al. Whole-body hybrid PET with 18F-FDG in the staging of non-Hodgkin’s lymphoma. J Nucl Med 2001;42(4):601–608. 147. Körholz D, Kluge R, Wickmann L , et al. Importance of F18-fluorodeoxy- D-2-glucose positron emission tomography (FDG-PET) for staging and therapy control of Hodgkin’s lymphoma in childhood and adolescence— consequences for the GPOH-HD 2003 protocol. Onkologie 2003;26:489– 493. 148. Klein M, Fox M, Kopelewitz B, et al. Role of FDG PET in the follow up of pediatric lymphoma. Presented at the 51 st annual meeting of the Society of Nuclear Medicine 2004:378. 149.Tatsumi M, Miller JH, Wahl RL. Initial assessment of the role of FDG PET in pediatric malignancies. Presented at the 51 st annual meeting of the Society of Nuclear Medicine 2004:383. 150.Hudson MM, Krasin MJ, Kaste SC. PET imaging in pediatric Hodgkin’s lymphoma. Pediatr Radiol 2004;34:190–198. 151.Krasin MJ, Hudson MM, Kaste SC. Positron emission tomography in pedi- atric radiation oncology: integration in the treatment-planning process. Pediatr Radiol 2004;34:214–221. F. Ponzo and M. Charron 521 152.Franzius C, Schober O. Assessment of therapy response by FDG-PET in pediatric patients. Q J Nucl Med 2003;47(1):41–45. 153. Kahkonen M, Metsahonkala L, Minn H, et al. Cerebral glucose metabo- lism in survivo rs of childhood acute lymphoblastic leukemia. Cancer 2000;88:693–700. 154. Briganti V, Sestini R, Orlando C, et al. Imaging of somatostatin receptors by indium-111-pentetreotide correlates with quantitative determination of somatostatin receptor type 2 gene expression in neuroblastoma tumor. Clin Cancer Res 1997;3:2385–2391. 155. Shulkin BL, Hutchinson RJ, Castle VP, et al. Neuroblast oma: positron emission tomography with 2- (fluorine-18)-fluoro-2-deoxy-D-glucose compared with metaiodobenzylguanidine scintigraphy. Radiology 1996; 199:743–750. 156. Kushner BH, Yeung HW, Larson SM, et al. Extending positron emission tomography scan utility to high risk neuroblastoma: fluorine-18 fluo- rodeoxyglucose positron emission tomography as sole imaging modality in follow-up of patients. J Clin Oncol 2001;19:3397–3405. 157. Shulkin BL, Wieland DM, Castle VP, et al. Carbon-11 epinephrine PET imaging of neuroblastoma. J Nucl Med 1999;40:129P. 158. Vaidyanathan G, Affleck DJ, Zalutsky MR. Validation of 4-(fluorine-18) fluoro-3-iodobenzylguanidine as a positron-emitting analog of MIBG. J Nucl Med 1995;36:644–650. 159. Ott RJ, Tait D, Flower MA, et al. Treatment planning for 131I-mIBG radio- therapy of neural crest tumors using 124I-mIBG positron emission tomog- raphy. Br J Radiol 1992;65:787–791. 160. Shulkin BL, Chang E, Strouse PJ, et al. PET FDG studies of Wilms’ tumors. J Pediatr Hematol Oncol 1997;19:334–338. 161.Frouge C, Vanel D, Coffre C, et al. The role of magnetic resonance imaging in the evaluation of Ewing sarcoma—a report of 27 cases. Skeletal Radiol 1988;17:387–392. 162 .MacVicar AD, Olliff JFC, Pringle J, et al. Ewing sarcoma: MR imaging of chemotherapy-induced changes with histologic correlation. Radiology 1992;184:859–864. 163. Lemmi MA, Fletcher BD, Marina NM, et al. Use of MR imaging to assess results of chemotherapy for Ewing sarcoma. AJR 1990;155:343– 346. 164. Erlemann R, Sciuk J, Bosse A, et al. Response of osteosarcoma and Ewing sarco ma to preoperative chemotherapy: assessment with dynamic and static MR imaging and skeletal scintigraphy. Radiology 1990;175:791– 796. 165.Holscher HC, Bloem JL, Vanel D, et al. Osteosarcoma: chemotherapy- induced changes at MR imaging. Radiology 1992;182:839–844. 166. Lawrence JA, Babyn PS, Chan HS, et al. Extremity osteosarcoma in child- hood: prognostic value of radiologic imaging. Radiology 1993;189:43– 47. 167. Watanabe H, Shinozaki T, Yanagawa T, et al. Glucose metabolic analysis of musculoskeletal tumours using 18fluorine-FDG PET as an aid to pre- operative planning. J Bone Joint Surg Br 2000;82:760–767. 168. Wu H, Dimitrakopoulou-Strauss A, Heichel TO, et al. Quantitative eval- uation of skeletal tumours with dynamic FDG PET: SUV in comparison to Patlak analysis. Eur J Nucl Med 2001;28:704–710. 169. Daldrup-Link HE, Franzius C, et al. Whole-body MR imaging for detec- tion of bone metastases in children and young adults: comparison with skeletal scintigraphy and FDG PET. AJR 2001;177:229–236. 522 Chapter 28 Current Research Efforts 170.Franzius C, Daldrup-Link HE, Sciuk J, et al. FDG-PET for detection of pul- monary metastases from malignant primary bone tumors: comparison with spiral CT. Ann Oncol 2001;12:479–486. 171.Franzius C, Sciuk J, Daldrup-Link HE, et al. FDG-PET for detection of osseous metastases from malignant primary bone tumours: comparison with bone scintigraphy. Eur J Nucl Med 2000;27:1305–1311. 172.Franzius C, Daldrup-Link HE, Wagner-Bohn A, et al. FDG-PET for detec- tion of recurrences from malignant primary bone tumors: comparison with conventional imaging. Ann Oncol 2002;13:157–160. 173. Lenzo NP, Shulkin B, Castle VP, et al. FDG-PET in childhood soft tissue sarcoma. J Nucl Med 2000;41(5 suppl):96P. 174.Abdel-Dayem HM. The role of nuclear medicine in primary bone and soft tissue tumors. Semin Nucl Med 1997;27:355–363. 175. Shulkin BL, Mitchell DS, Ungar DR, et al. Neoplasms in a pediatric pop- ulation: 2-(F-18)-fluoro-2-deoxy-D-glucose PET studies. Radiology 1995; 194:495–500. 176.Hawkins DS, Rajendran JG, Conrad III EU, et al. Evaluation of chemother- apy response in pediatric bone sarcomas by (F-18)-fluorodeoxy-D-glucose positron emission tomography. Cancer 2002;94:3277–3284. 177. Even-Sapir E, Metser U, Flusser G, et al. Assessment of malignant skele- tal disease: initial experience with 18F-fluoride PET/CT and comparison between 18F-fluoride PET and 18F-fluoride PET/CT. J Nucl Med 2004; 45:272–278. 178. Franzius C, Hotfilder M, Herma nn S, et al. Feasibility of high resolution animal PET of Ewing tumors and their metastasis in a NOD/SCID mouse model. Presented at the 51 st annual meeting of the Society of Nuclear Med- icine 2004:382. 179. Ben Arush MW, Israel O, Kedar Z, et al. Detection of isolated distant metastasis in soft tissue sarcoma by fluorodeoxyglucose positron emis- sion tomography: case report. Pediatr Hematol Oncol 2001;18(4):295– 298. 180. Lucas JD, O’Doherty MJ, Cronin BF, et al. Prospective evaluation of soft tissue masses and sarcomas using fluorodeox yglucose positron emission tomography. Br J Surg 1999;86:550–556. 181. Lucas JD, O’Doherty MJ, Wong JC, et al. Evaluation of fluorodeoxyglu- cose positron emission tomography in the management of soft-tissue sar- comas. J Bone Joint Surg Br 1998;80:441–447. 182. Bredella MA, Caputo GR, Steinbach LS. Value of FDG positron emission tomography in conjunction with MR imaging for evaluating therapy response in patients with musculoskeletal sarcomas. AJR 2002;179: 1145–1150. 183. Pacak K, Eisenhofer G, Carrasquillo JA, et al. 18-6-(18F)fluorodopamine positron emission tomographic (PET) scanning for diagnostic localization of pheochromocytoma. Hypertension 2001;38:6–8. 184. Sabbaga CC, Avilla SG. Schulz C, et al. Adrenocortical carcinoma in chil- dren: clinical aspects and prognosis. J Pediatr Surg 1993;28:841–843. 185. Evans HL, Vassilopoulou-Sellin R. Adrenal cortical neoplasms. A study of 56 cases. Am J Clin Pathol 1996;105:76–86. 186.Maurea S, Mainolfi C, Wang H, et al. Positron emission tomography (PET) with fludeoxyglucose F 18 in the study of adrenal masses: comparison of benign and malignant lesions. Radiol Med 1996;92:782–787. 187. Boland GW, Goldberg MA, Lee MJ, et al. Indeterminate adrenal mass in patients with cancer: evaluation at PET with 2-(F-18)-fluoro- 2–deoxy-glucose. Radiology 1995;194:131–134. F. Ponzo and M. Charron 523 188. Kreissig R, Amthauer H, Krude H, et al. The use of FDG-PET and CT for the staging of adrenocortical carcinoma in children. Pediatr Radiol 2000; 30:306. 189. Philip I, Shun A, McCowage G, Howman-Giles R. Positron emission t omography in recurrent hepatoblastoma. Pediatr Surg Int 2005;21(5): 341–345. 524Chapter 28 Current Research Efforts Section 5 Imaging Atlas 29 PET–Computed Tomography Atlas M. Beth McCarville Fluorine-18-fluorodeoxyglucose (FDG) positron emission tomography (PET) is a functional imaging modality that capitalizes on the fact that pathologic processes are generally highly metab olically active and accumulate more glucose (and FDG) than normal tissue. However, sites of normal metabolic activity can also demonstrate intense FDG uptake and can sometimes be difficult to distinguish from disease activity. Fusion imaging modalities that acquire both functional and correlative anatomic imaging provide an important advantage over PET alone because they allow the accurate anatomic localization of sites of increased FDG activity (1–5). In this chapter, normal sites of FDG activ- ity are correlated with computed tomography (CT) anatomy in images obtained during PET-CT scanning. Examples of pathologic FDG activ- ity are included to illustrate the unique value of this fusion imaging modality in distinguishing normal from pathologic activity. Head and Neck Identifying normal FDG activity in the head and neck, as elsewhere in the body, is aided by its bilaterally symmetric distribution. Because the brain is exclusively dependent on glucose metabolism, it accumulates intense FDG activity. Accumulation is greatest in the cerebral cortex, basal ganglia, thalamus, and cerebellum (Figs. 29.1 and 29.2). Intense activity is sometimes present, not only in the brain, but also in the ocular muscles and optic nerves (Fig. 29.2). Because FDG is known to accu- mulate in saliva (6,7), minimal to moderate activity may be present in the salivary and parotid glands (Fig. 29.3). Fluorodeoxyglucose uptake also occurs in the lymphatic tissues of the pharynx, specifically within the Waldeyer ring, which consists of the nasopharyngeal, palatine, and lingual tonsils (Fig. 29.3). In patients who are tense, FDG activity may be very prominent in the neck muscles secondary to contraction- induced metabolic activity. Fluorodeoxyglucose activity in the normal thyroid gland is usually absent or minimal but can be prominent. Intrin- sic laryngeal muscles of phonation can exhibit intense FDG activity 527 [...]... and Kostakoglu et al (2) describe the clinical applications of PET in oncology in adult patients As more experience is gained in the pediatric population, indications for pediatric FDG -PET imaging are emerging (3–5) As with any other nuclear imaging modality, it is very important to recognize artifacts while reading the whole-body FDG -PET images for the subsequent correct management of patients Recognition... discusses the normal biodistribution of FDG in pediatric patients, common artifacts seen on whole-body FDG -PET images, common causes of false-positive and false-negative findings, and recognition of artifacts Scanning Protocol Performing FDG -PET studies on pediatric patients presents a special challenge The issues that require consideration specifically in the pediatric population include intravenous access,... specific to pediatric PET imaging have been dealt with in recent articles (6–8) Procedure guidelines and patient preparation techniques for the adult FDG -PET imaging have been published in the literature (9–11) Institutions performing PET studies on pediatric patients are recommended to consult these reports and to develop their own protocols Essentially, patient preparation is the same for pediatric. .. Axial PET- CT images show FDG activity in both supraclavicular brown fat (arrows) and pathologic supraclavicular nodes (arrowheads) This example illustrates the value of PET- CT in identifying adenopathy that may be difficult to distinguish from physiologic brown fat activity on PET alone B A C Figure 29.7 A: MIP anterior PET image shows normal thymic contour and FDG activity (arrow) in a 3-year-old girl... 1998;171: 1103 –1 110 3 Charron M, Beyer T, Bohnen NN, et al Image analysis in patients with cancer studied with a combined PET and CT scanner Clin Nucl Med 2000; 25:905– 910 4 Bar-Shalom R, Yefremov N, Guralnik L, et al Clinical performance of PET/ CT in evaluation of cancer: additional value for diagnostic imaging and patient management J Nucl Med 2003;44:1200–1209 5 Townsend DW, Beyer T A combined PET/ CT... skeleton: MR imaging study Radiology 1990;177:83–88 Sugawara Y, Fisher SJ, Zasadny KR, et al Preclinical and clinical studies of bone marrow uptake of fluorine- 1- uorodeoxyglucose with or without granulocyte colony-stimulating factor during chemotherapy J Clin Oncol 1998;16:173–180 30 Common Artifacts on PET Imaging Peeyush Bhargava and Martin Charron Whole-body positron emission tomography (PET) with... quadrilateral-shaped configuration with homogeneous density In B A C Figure 29.5 A: Maximum intensity projection (MIP) image showing intense, symmetric activity in the supraclavicular regions (arrow) B,C: Axial PET- CT images allow localization of this activity to supraclavicular brown fat (arrows) This finding is common in pediatric patients M.B McCarville A 531 B Figure 29.6 A 26-year-old woman with non-Hodgkin’s... chest region Eur J Nucl Med Mol Imaging 2002;29:1393–1398 Cohade C, Osman M, Pannu HK, et al Uptake in supraclavicular area fat (“USA-Fat”): description on 18F-FDG PET/ CT J Nucl Med 2003;44: 170–176 Hedlund GL, Kirks DR Respiratory system In: Kirks DR, ed Practical Pediatric Imaging, 2nd ed Cincinnati: Little, Brown, 1991:517–707 Gordon BA, Flanagan FL, Dehdashti F Whole-body positron emission tomography:... An 18-year-old woman under treatment for rhabdomyosarcoma who had recently received granulocyte colony-stimulating factor (GCSF) MIP anterior image shows marrow activity that is diffusely increased relative to the liver This pattern of marrow activity is commonly seen in patients receiving G-CSF M.B McCarville R A 541 L B Figure 29.23 This example illustrates the value of correlative PET- CT imaging. .. is seen A B Figure 29 .10 A,B: Axial PET- CT images show normal FDG activity in the crus of the left diaphragm (straight arrows) and normal, homogeneous FDG uptake within the liver (curved arrows) and spleen (arrowheads) The spleen usually shows activity that is equal to or less than that of the liver 534 A Chapter 29 PET Computed Tomography Atlas B Figure 29.11 A,B: Axial PET- CT images show a focal . lym- phoma: detection with FDG -PET versus CT. Radiology 1998;206:475– 481. 129.Moog F, Bangerter M, Diederichs CG, et al. Lymphoma: role of whole- body 2-deoxy- 2-( F-18)fluoro-D-glucose (FDG) PET. malignancy grade with PET in non-Hodgkin’s lymphoma. J Nucl Med 1995;36:1790–1796. 133. Newman JS, Francis IR, Kaminski MS, et al. Imaging of lymphoma with PET with 2-( F-18 )- uoro-2-deoxy-D-glucose: correlation. Neoplasms in a pediatric pop- ulation: 2-( F-18 )- uoro-2-deoxy-D-glucose PET studies. Radiology 1995; 194:495–500. 176.Hawkins DS, Rajendran JG, Conrad III EU, et al. Evaluation of chemother- apy response