Indian Journal of Nuclear Medicine
Home | About IJNM | Search | Current Issue | Past Issues | Instructions | Ahead of Print | Online submissionLogin 
Indian Journal of Nuclear Medicine
  Editorial Board | Subscribe | Advertise | Contact
Users Online: 242 Print this page  Email this page Small font size Default font size Increase font size

 Table of Contents     
Year : 2021  |  Volume : 36  |  Issue : 3  |  Page : 327-339  

Spectrum of flurodeoxyglucose positron emission tomography/computerized tomography findings in tumors and tumor-like conditions of the musculoskeletal system

Department of Nuclear Medicine and Molecular Imaging, Tata Memorial Hospital, Homi Bhabha National University (HBNI), Mumbai, Maharashtra, India

Date of Submission24-Dec-2020
Date of Decision12-Feb-2021
Date of Acceptance24-Feb-2021
Date of Web Publication23-Sep-2021

Correspondence Address:
Dr. Nilendu C Purandare
Department of Nuclear Medicine and Molecular Imaging, Tata Memorial Hospital, Homi Bhabha National University (HBNI), Parel, Mumbai - 400 012
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijnm.ijnm_242_20

Rights and Permissions

Bone and soft-tissue tumors display a wide range of metabolic activity on flurodeoxyglucose positron emission tomography/computerized tomography (FDG PET/CT) imaging due to their varying histopathological features. Several benign tumors show high FDG uptake similar to that seen in malignant lesions and their metabolic characteristics can overlap. Certain benign tumors can potentially undergo malignant transformation and FDG PET/CT can play an important role in detecting malignant change. The intensity of metabolic activity on FDG PET/CT correlates with histological grade of malignant tumors and also acts as a valuable prognostic factor. FDG PET/CT plays an important role in the staging work up of bone and soft-tissue malignancies. It has been found to be superior to conventional imaging techniques primarily for detecting distant metastatic disease. Because of its ability to detect metabolic changes, FDG PET/CT is a very useful in assessing response to treatment. Metabolic response seen on FDG PET is a powerful surrogate marker of histopathological response to chemotherapy. The purpose of this article is to study the variable patterns of FDG uptake in tumors of the musculoskeletal system, describe the clinical utility of FDG PET/CT in predicting malignant change in benign tumors and discuss its role in staging, response assessment, and prognostication of malignant lesions.

Keywords: Bone, flurodeoxyglucose positron emission tomography/computerized tomography, musculoskeletal, soft-tissue, tumors

How to cite this article:
Purandare NC, Shah S, Agrawal A, Puranik A, Rangarajan V. Spectrum of flurodeoxyglucose positron emission tomography/computerized tomography findings in tumors and tumor-like conditions of the musculoskeletal system. Indian J Nucl Med 2021;36:327-39

How to cite this URL:
Purandare NC, Shah S, Agrawal A, Puranik A, Rangarajan V. Spectrum of flurodeoxyglucose positron emission tomography/computerized tomography findings in tumors and tumor-like conditions of the musculoskeletal system. Indian J Nucl Med [serial online] 2021 [cited 2021 Dec 8];36:327-39. Available from:

   Introduction Top

Tumors of the bone and soft-tissue encompass a wide range of benign and malignant pathologies. Imaging modalities such as plain radiographs, computerized tomography (CT) scan, and magnetic resonance imaging (MRI) are routinely used to evaluate these tumors. Majority of the tumors of the musculoskeletal (msk) system have well-documented morphological imaging features that help in diagnosis, characterization, staging, and treatment planning. Flurodeoxyglucose positron emission tomography (FDG PET) and PET/CT is an established imaging modality in evaluation of several malignancies. Both benign and malignant msk tumors display variable metabolic characteristics on FDG PET/CT imaging owing to their unique histopathological features. In the context of bone and soft-tissue tumors, the role of FDG PET/CT in establishing diagnosis, staging, response evaluation, prognostication, and predicting histological grade is still evolving unlike its established role in several other cancers. With the ever increasing use of FDG PET/CT across a variety of clinical conditions, it is important to get familiarized with its role and scope in msk tumors and also learn about the common diagnostic dilemmas and pitfalls likely to be encountered in routine clinical practice.

   Benign Bone Lesions and Flurodeoxyglucose Uptake Top
[Table 1]
Table 1: Flurodeoxyglucose uptake in commonly b encountered benign bone and soft-tissue lesions

Click here to view

Lesions with high flurodeoxyglucose uptake

Benign tumors show a wide range of metabolic activity on FDG PET/CT studies based on their varied histologies. A few mechanisms have been proposed and believed to be the cause of intense FDG concentration in certain benign tumors. The cellular composition of many benign bone tumors contains histiocytes and giant cells which belong to the monocyte-macrophage lineage.[1],[2] Energy for these cells is predominantly provided by intracellular glucose mechanism[3],[4] which is the cause of high intratumoral concentration of FDG on PET studies. Tumors which have abundance of histiocytes and giant cells and show high FDG avidity include chondroblastomas [Figure 1], osteoblastomas [Figure 2], giant cell tumors [Figure 3], and aneurysmal bone cysts.[5],[6],[7] Brown tumors which are not true tumors are lytic bone lesions formed due to increased osteoclastic activity caused by excess secretion of parathyroid hormone in end stages of primary and secondary hyperparathyroidism. Brown tumors are histologically similar to giant cell tumors and show FDG uptake due to the presence of giant cells and macrophages [Figure 4]. Reduction of FDG uptake in brown tumors is noted after treatment for hyperparathyroidism.[8]
Figure 1: Chondroblastoma in a 24 year old man with complaints of pain around the knee. (a) Coronal reformatted CT image shows a well defined lytic lesion with a narrow zone of transition and a sclerotic rim in the epiphyseal region of the lower end of the tibia with specks of calcification (arrow). (b) Axial FDG PET/CT shows intense FDG uptake in the chondroblastoma (arrow) with a SUVmax of 12.5. Chondroblastomas are known to concentrate FDG

Click here to view
Figure 2: Osteoblastoma in a cervical vertebra of a 21 year old lady with neck pain. (a) Axial CT image shows a well defined lytic lesion in the articular process (arrow) with central calcification. (b) Axial FDG PET/CT shows intense FDG uptake in the osteoblastoma (arrow) with SUVmax of 11. Osteoblastomas are FDG avid benign bone tumors

Click here to view
Figure 3: GCT of the tibia in a 28 year old manwho presented with pain around the knee. (a) Plain radiograph (antero-posterior view) shows a well defined sub-articular lytic lesion in the upper end of the tibia (arrow). (b) Coronal FDG PET/CT shows intense FDG uptake in the lesion (arrow) with SUVmax of 22.2. GCT's are FDG avid benign bone tumors

Click here to view
Figure 4: Brown tumor in a 34 year oldfemale with primary hyperparathyroidism who presented with neck swelling and bone pains. (a) CT shows an expansile lytic lesion in the posterior aspect of the rib (arrow).(b) FDG PET/CT shows high FDG uptake in the lytic brown tumor. (c) CT shows a well defined enhancing parathyroid adenoma (arrow). (d) FDG PET/CT shows low grade FDG uptake in the parathyroid adenoma

Click here to view

Osteoid osteomas are benign lesions that can show intense FDG uptake.[9] The nidus of painful osteoid osteomas show increased cyclooxygenase-2 expression.[10] Pain associated with osteoid osteomas is due to release of prostaglandins as a direct result of high levels of cyclooxygenase-2. Increased levels of prostaglandins cause vasodilation in the vascular nidus, this increased blood supply causes increased recruitment of inflammatory cells, which are known to utilize glucose for their energy requirements. This could be one of the mechanisms explaining high FDG uptake in painful osteoid osteomas [Figure 5].[11] Percutaneous radiofrequency ablation (RFA) has become a preferred treatment modality for many of the benign tumors such as osteoid osteoma, chondroblastoma, and osteoblastoma to relieve pain and to prevent further growth.[12],[13],[14] High concentration of FDG in these benign lesions can form the basis of using FDG PET/CT as an imaging tool to monitor response to RFA. RFA causes coagulation necrosis in the ablated lesion and destruction of its metabolic pathways. Resolution of FDG uptake after RFA can thus be used as a surrogate marker of completeness of ablation.[11]
Figure 5: Osteoid Osteoma of the ischio-pubic ramus in a 14 year old girlwho presented with right hip pain. (a) Axial CT image shows a well defined lucency with a central sclerotic nidus (arrow). (b) Axial FDG PET/CT shows intense FDG uptake in the nidus of the OO with SUVmax of 10.5. Nidus of painful OO concentrates FDG

Click here to view

In lesions, such as fibrous dysplasia [Figure 6] and other fibrous tumors such as cortical desmoid, desmoplastic fibroma, nonossifying fibroma/fibrous cortical defect [Figure 7], and osteofibrous dysplasia fibroblasts are the predominant proliferating cells. Although giant cells are present in some amounts around degenerative foci in these lesions, it is the actively proliferating fibroblasts that are responsible for high concentration of FDG.[6],[15],[16] Variation in the intensity of FDG uptake in various fibrous lesions and also among the tumors belonging to the same histology can be attributed to the difference in the amount of actively proliferating fibroblasts.
Figure 6: Incidentally detected FD in a 42 year old man with malignancy of the oral cavity. (a) Coronal reformatted CT image shows ground glass change in the expanded marrow of the right femoral shaft (arrow). (b) Coronal FDG PET/CT shows FDG avidity in the ground glass changes of FD (arrow) with SUVmax of 6.7. Actively proliferating fibroblasts of FD concentrate FDG

Click here to view
Figure 7: Incidentally detected non-ossifying fibroma in a 12 year old boy with Ewings sarcoma of the clavicle. (a) Coronal reformatted CT shows a well definedcorticalbased lytic lesion with a sclerotic rim in the proximal femoral shaft (arrow) with a SUVmax of 2.6. (b) Coronal FDG PET/CT shows focal FDG uptake in the lesion (arrow) with a SUVmax of. NOF's are known to concentrate FDG

Click here to view

It should be borne in mind that many benign bone lesions whether slow growing and indolent or aggressive can show higher tracer uptake compared to certain malignant bone tumors. Thus, the intensity of metabolic activity should not be considered as a pointer toward malignancy while evaluating such lesions and emphasis should be given to the radiographic and CT features to look for signs of aggressive malignant traits.[17]

Lesions with low flurodeoxyglucose uptake

Benign cartilaginous tumors such as enchondroma and osteochondroma [Figure 8] show low concentration of FDG in most instances.[5],[6],[18],[19] Studies have shown that as compared to other benign tumors, cartilaginous tumors both benign as well as their malignant counterparts show a surprising paucity of FDG uptake. The primary reason for this can be attributed to the histological nature and cell type of these tumors. Cartilage tumors show relative hypovascularity, have a matrix which is gelatinous[19] and are hypocellular with high water content. These factors contribute to poor FDG uptake in majority of cartilage tumors, though occasionally one could come across a lesion with relatively higher metabolism [Figure 9]. Intraosseous lipomas and hemangiomas [Figure 10] are other benign lesions which show poor FDG uptake which could be attributed to their indolent, nonaggressive nature with low cellularity and metabolism.
Figure 8: Osteochondroma in a 28 year old man who presented with swelling in the leg. (a) Axial CT shows an exophytic osteochondral lesion arising from the fibula (arrow). (b) Axial FDG PET/CT show no significant FDG uptake within the lesion, SUVmax 2.0. Osteochondromas show poor FDG concentration

Click here to view
Figure 9: Enchondroma in a 44 year old lady with pain around the knee. (a) Sagittal reformatted CT image shows a lesion in the femur with characteristic chondroid calcification (arrow). (b) Sagittal FDG PET/CT show moderate grade FDG uptake in the enchondroma (arrow), SUVmax3.2. Majority of enchondromas show poor FDG concentration with occasional lesion showing moderate to high uptake

Click here to view
Figure 10: Incidentally detected vertebral hemangioma in 20 yearoldman with ewing's sarcoma. (a) Axial CT image shows a well definedtrabaculated lesion in the vertebral body. (b) Axial FDG PET/CT image shows low grade FDG uptake in the hemangioma with SUVmax of 1.2. Hemangiomas show poor or low FDG uptake

Click here to view

   Benign Soft-Tissue Lesions and Flurodeoxyglucose Uptake Top
[Table 1]

FDG is known to concentrate in certain benign soft tissue tumors and tumor like conditions. Hibernoma is a benign tumor of brown fat origin that has morphological imaging characteristics similar to other fat containing tumors such as lipoma and liposarcoma. Brown fat is a producer of heat and contains large quantities of mitochondria and hence is highly metabolic, the primary reason for high FDG avidity of hibernomas [Figure 11].[20],[21] Differentiating hibernoma from liposarcomas can be tricky with overlapping features on CT, MRI as well as on FDG PET since liposarcomas show high FDG uptake. Variations and fluctuations in the standardized uptake value (SUV) of FDG concentration over time in hibernomas can be useful in differentiating them from malignant fat containing tumors.[21]
Figure 11: Incidentally detected hibernoma in a 37 year old lady with breast cancer. (a) Axial CT image shows a well defined subcutaneous fat density lesion in the lumbar lesion, with areas of soft tissue attenuation within (arrow). (b) Axial FDG PET/CT shows intense FDG uptake in the hibernoma with a SUV maxof 22. Hibernomas are tumors of brown adipose tissue and highly metabolic in nature

Click here to view

Elastofibroma dorsi (EFD) is a benign soft-tissue tumor located in the inferior scapular region. EFD can be bilateral or unilateral, majority are asymptomatic and incidentally detected on imaging, though occasionally they can present as painful lumps.[22] EFD are known to concentrate FDG and are often seen as hypermetabolic soft-tissue lesions in the inferior scapular region [Figure 12] when PET/CT scans are performed for other indications.[23],[24] The mechanism of FDG uptake in EFD is uncertain, one of the possible mechanisms could be the accumulation and proliferation of abnormal elastic fibers,[25] high vascularity, and increased metabolic activity. Due to their hypermetabolic nature, EFD can be erroneously interpreted as metastatic soft tissue deposits during an oncologic PET/CT examination. Typical location in the inferior scapular region, CT appearance of a lenticular shaped lesion isoattenuating to the surrounding musculature with hypodense fatty striations[26] and stability of FDG avidity over serial PET scans[27] can be useful in differentiating EFD from malignant lesions and prevent unnecessary biopsies.

Tumors of the nerve sheath such as schwannoma and neurofibroma are not infrequently seen during whole body PET/CT examination either as incidental findings or when the study is performed to evaluate hereditary conditions such as neurofibromatosis-1 (NF-1). Both schwannoma and neurofibroma whether sporadic or as a part of a hereditary syndrome can show varying degrees of FDG uptake. Schwannomas are benign, slow growing tumors arising from the nerve sheath usually in the extremities or the head-neck region[28] and less commonly in the chest and abdomen. The exact reason for high FDG uptake in schwannomas is unclear: Overexpression of glucose transporter protein-type 3 (GLUT 3) which is one of the major glucose transporters on neuronal surface could provide an explanation,[29] but this is yet to be conclusively proven. FDG uptake in schwannomas can be variable ranging from low grade to highly FDG avid tumors [Figure 13]. This wide range of FDG uptake can be explained by tumor cellularity, hypercellular tumors showing high SUV compared to hypocellular tumors.[29] Heterogeneity of uptake is also a feature seen in schwannomas particularly in larger tumors which frequently exhibit cystic and necrotic changes. FDG uptake in smaller lesions tends to be more homogeneous. Neurofibromas are also benign tumors arising from the nerve sheath and can be sporadic in nature or as a part of a neurocutaneous syndrome like NF-1. They show a more homogeneous pattern of FDG uptake [Figure 14] which is uniformly low compared to that observed in schwannomas.[30] Multiple nerve sheath tumors located in regions such as neck, mediastinum, and retroperitoneum can mimic more sinister pathology like lymph nodes or soft tissue deposits in patients with a known malignancy. This diagnostic pitfall should be borne in mind during PET/CT interpretation.
Figure 12: Incidentally detected elastofibroma dorsi in a 23 year old lady with ewingssarcoma of the thumb. (a) Axial CT image shows aisodense soft tissue nodule adjacent to the medial scapular margin (arrow). (b) Axial FDG PET/CT image shows intense FDG uptake in the nodule (arrow) with SUVmax of 9.2. Biopsy confirmed diagnosis of EFD. EFD's are benign tumors that concentrate FDG

Click here to view
Figure 13: Schwannoma in a 47 year old man with complaints of right sided chest pain.(a) Coronal reformatted CT image shows a well demarcated heterogenously enhancing extrapleural mass in the region of the lung apex with cystic areas within (arrow). (b) Coronal FDG PET/CT image shows high but heterogenous FDG uptake in the mass with SUVmax of 7.0. Biopsy confirmed the diagnosis of schwannoma.Heterogeneity of FDG uptake can be seen in schwannomas due to cystic changes

Click here to view
Figure 14: Multiple neurofibrommas in a 36 year old lady with NF-1. (a) Coronal reformatted CT image shows well defined enhancing soft tissue masses in the neck and the thoracic wall (arrows). (b) Coronal FDG PET/CT image shows high and fairly homogenous FDG uptake in the masses with average SUVmax of 6.5 (arrows).Neurofibromas are known to concentrate FDG

Click here to view

Langerhans cell histiocytosis (LCH) is a multisystem disorder in which lesions demonstrate increased FDG uptake [Figure 15] as they contain abundance of histiocytes and giant cells. Since treatment decisions are dictated by the presence of solitary versus multiple bone lesions, FDG PET can impact management by identifying multifocal skeletal disease more effectively compared to conventional imaging.[31] In addition, it can act as a prognostic marker by detecting disease in high risk organs such as liver, spleen, and lungs. FDG PET/CT can monitor response to systemic therapy in LCH by demonstrating reduction in metabolic activity in patients who are good responders.
Figure 15: Multisystem involvement in a 36 year old lady with LCH. (a) Coronal reformatted CT image shows multiple lytic lesions in tibia bilaterally (arrows). (b) Coronal FDG PET/CT shows FDG avidity in the tibial lesions (arrows). (c)Axial PET/CT shows a FDG avid inguinal node involved by disease (arrow). (d) Axial CT in lung window settings shows cystic areas in the lungs(arrows). FDG PET/CT can demonstrate multisystem involvement in LCH

Click here to view

   Prediction of Malignant Change by Positron Emission Tomography/Computerized Tomography Top

FDG PET/CT has the potential to detect malignant change in certain benign bone and soft-tissue tumors. Although many benign tumors show high degree of FDG uptake there are certain chondroid lesions such as enchondroma and osteochondroma which show a relative paucity of FDG uptake. These benign chondroid tumors can undergo malignant or sarcomatous transformation, which can be seen as foci of high FDG uptake within a relatively hypometabolic background [Figure 16]. FDG PET/CT is a promising tool to predict malignant change and to differentiate benign from malignant osteochondromas.[32],[33] The differentiation between a benign osteochondroma and a grade I chondrosarcoma is often difficult because both lesions often display lower relative paucity of FDG uptake. Lesions which show a malignant change to grade II/grade III or de-differentiated chondrosarcoma show a significantly higher FDG uptake as compared to benign lesions. In patients with multiple hereditary exostoses who are clinically symptomatic for malignant change, PET can detect early malignant change at other clinically asymptomatic sites in addition to confirming sarcomatous transformation at the suspected site. FDG PET/CT by directing percutaneous biopsy from the metabolically avid part of the lesion can be used to obtain the most biologically representative sample for histological analysis. This approach can avoid biopsies from nonrepresentative areas and the possibility of incorrect or missed diagnosis [Figure 16].
Figure 16: 34 year old man with known osteochondroma of the rib with complaints of recent onset chest pain. (a) CT shows a osteochondral lesion arising from the costovertebral region with an associated soft tissue mass (arrows).(b) FDG PET/CT shows an intense focus of uptake within the mass suggesting a malignant change (arrow). Arrowhead shows FDG avidity in the atelectatic component of thelung.(c)CT guided biopsy from the FDG avid focus (arrow) confirmed the diagnosis of grade II chondrosarcoma

Click here to view

Detecting malignant transformation in benign nerve sheath tumors is clinically challenging and morphologic imaging cannot reliably differentiate benign lesions from the malignant transformed ones. FDG PET/CT has been found to be useful in detecting early malignant transformation in benign peripheral nerve sheath tumors particularly in patients with neurocutaneous syndromes like NF-1. A nerve sheath tumor that shows focal FDG uptake that is much intense compared to rest of the lesions is likely to have undergone a sarcomatous change [Figure 17]. Both visual qualitative PET assessment and use of semi-quantitative SUV cutoff have shown good diagnostic accuracy.[34],[35],[36] However, due to the lack of set criteria for visual interpretation and variability of SUV cut offs, its use is somewhat restricted in clinical practice.
Figure 17: 30 year old man with NF-1 presented with gradually increasing upper thigh swelling. (a) Axial CT shows infiltrative subcutaneous soft tissue thickening consistent with plexiform neurofibroma (arrow). Necrotic soft tissue is seen within the neurofibroma (arrowhead). (b) Axial FDG PET/CT shows diffuse and uniform low grade FDG uptake in the plexiform neurofibroma (arrow) and intense uptake (SUVmax 15.2) in the necrotic mass, biopsy from which confirmed malignant peripheral nerve sheath tumor

Click here to view

Paget's disease is characterized by abnormal and excessive remodeling of the bone.[37] Plain radiographs are the main stay of diagnosis and classical findings are described depending on the phase of the disease. Due to increased vascularity and remodeling the bone lesions show increased radionuclide uptake on bone scintigraphy. Paget's disease is not associated with increased FDG uptake in majority of patients though rarely hypermetabolism can be seen in more active cases.[38] Sarcomatous transformation is one of the rare but dreaded complications seen in long standing disease. The relative paucity of FDG uptake in pagetoid lesions can aid in localizing the site of malignant transformation which will demonstrate high FDG uptake associated with sarcomas [Figure 18].
Figure 18: 70 year old man with Pagets disease presented with complaints of pain in the left thigh. (a) Maximum intensity projection (MIP) image of a 18F Sodium fluoride (NaF) PET/CT scan shows increased tracer uptake in several skeletal sites(arrows) representing increased bone turnover of Pagets disease. (b) and (c) Coronal and axial NaF PET/CT images show increased tracer uptake in the left femur and the sacrum (arrows). 70 year old man with Pagets disease presented with complaints of pain in the left thigh. (d) and (e), MIP and coronal FDG PET/CT imagesof the same patient shows increased FDG uptake in the left femur corresponding to the site of sarcomatous transformation(arrows) with a SUVmax of 15.8. (f) Axial FDG PET/CT shows the absence of FDG uptake in rest of the pagetoid lesions (arrowheads in d and f).

Click here to view

   Flurodeoxyglucose Positron Emission Tomography/Computerized Tomography in Staging Malignant Tumors Top

Bone sarcomas such as Ewing's sarcoma (EWS) and osteogenic sarcoma (OS) show high rate of glycolysis and thereby high FDG uptake. FDG PET/CT is included in the standard metastatic work-up of EWS patients due to its high accuracy in detecting skeletal metastases [Figure 19]. Its sensitivity is significantly higher compared to bone scintigraphy for skeletal metastases.[39],[40] If no evidence of metastatic disease is seen on FDG PET/CT additional imaging investigations or procedures like bone marrow aspiration/biopsy can be avoided.[41] Thus, inclusion of FDG PET/CT in the metastatic work up of EWS has strong implications for staging and subsequent therapy planning.
Figure 19: 17 year old girl withEwings sarcoma of the tibia referred for baseline staging with FDG PET/CT. (a) Coronal MIP image shows FDG avid lesion in the right tibia (arrow) with a SUVmax of 10.9 and another smaller focus of FDG uptake in the right femur (arrowhead). (b) Sagittal FDG PET/CT image confirms the disease at the primary site in the tibia (arrow) and a marrow metastasis in the femur (arrowhead).

Click here to view

OS is FDG avid tumors and PET/CT has been used for initial staging work up. Studies have shown that FDG PET/CT has a better sensitivity compared to bone scan in detecting skeletal lesions of OS.[42],[43] FDG PET/CT scores over bone scintigraphy by detecting more metastatic lesions in the region of the growth plate in young adults [Figure 20], where the high physiological tracer uptake can mask metastatic disease on bone scans.[42] The incremental benefit of FDG PET/CT over bone scintigraphy observed in OS is not as pronounced as that seen in EWS.[39] This could be due to the different nature of metastases produced by the two sarcomas. Metastases of OS are bone forming or osteoblastic and are easily detected by bone scintigraphy, which has a high sensitivity for new bone/osteoid formation, whereas metastases of EWS predominantly infiltrate the marrow and characterized by osteoclastic activity. Owing to this the impact of FDG PET/CT on staging and therapy planning in OS is limited as compared to EWS.
Figure 20: 8 year old boy with osteogenic sarcoma of the femur referred for metastatic staging. (a) MIP image of a 18F NaF PET/CT scan shows increased tracer uptake at the primary site in the femur (arrow) and also linear uptake in the region of the growth plates in the distal femur and proximal tibia (arrowheads). (b) and (c) Saggital and axial sodium fluoride PET/CT images confirms the location of uptake to be in the physeal plates (arrowheads) 8 year old boy with osteogenic sarcoma of the femur referred for metastatic staging. (d) MIP image of FDG PET/CT in the same patient shows increased FDG uptake at the primary site (arrow) and focal uptake in the region of the growth plates in the distal femur and proximal tibia (arrowheads). (e) and (f) Saggital and axial FDG PET/CT confirms the focal nature of uptake in the physeal plates (arrowheads).

Click here to view

Soft-tissue sarcomas (STS) are histologically a heterogeneous group of malignant tumors. Majority of histological subtypes (98%) show FDG avidity which can vary in intensity based on their histopathological grade.[44] Since more than 75% of metastases in adult STS occur in the lungs, the role for metastatic work up beyond CT chest is questionable. Hence, FDG PET/CT is not routinely used in metastatic staging of adult STS. However, certain high-grade sarcomas have a higher propensity for nodal and skeletal metastases [Figure 21]. On such occasions, FDG PET/CT can be used for initial staging as it can potentially change management decisions by detecting distant metastases.
Figure 21: 15 year old girl with synovial sarcoma of the calf referred for baseline staging with FDG PET/CT. (a) Saggital reformatted CT image shows an illdefined soft tissue in the calf (arrow) and an enlarged popliteal node (arrowhead). (b) Saggital FDG PET/CT shows increased FDG uptake in the primary mass (SUVmax 14.9) (arrow) as well as the popliteal node (arrowhead). FDG PET/CT detects nodal and distant metastases in high grade soft tissue sarcoma

Click here to view

Pediatric tumors like rhabdomyosarcomas have a high risk of regional nodal metastases and regional nodal sampling is recommended during surgery.[45] FDG PET/CT is superior to conventional imaging in detection of regional nodal disease in RMS[39],[46] and identifies more diseased nodes with less indeterminate results. It also provides a better overall initial staging accuracy by identifying unsuspected distant metastases.[47]

Plasmacytoma and multiple myeloma (MM) are malignancies characterized by clonal proliferation of plasma cells. Both conditions demonstrate FDG avidity and PET/CT has been used for initial staging and assessing therapeutic response. Plasmacytoma can be confined to bone or occur in extramedullary locations. PET/CT due to its ability to scan the entire body is able to screen for additional lesions in patients who are presumed to have solitary plasmacytoma [Figure 22]. Such patients are also at higher risk for evolution to MM and thus PET/CT can potentially have an impact on clinical management by changing treatment to systemic therapy rather than localized surgery or radiation.[48],[49] In a patient presumed to have a clinical diagnosis of solitary plasmacytoma, when FDG PET/CT shows several FDG avid lytic lesions along with multiple foci of FDG uptake in the marrow, the findings are more likely to represent MM. In MM, FDG PET/CT is useful in initial staging as it can detect multiplicity of lesions, diffuse marrow involvement, as well as extramedullary disease. PET/CT is also used to image cases of smouldering MM, which is a mid-clinical stage, where it can predict rate of progression to established MM, which could be either slow and gradual or rapid and symptomatic.[50],[51]
Figure 22: 43 year old man with a rib lesion diagnosed as plamacytoma, underwent FDG PET/CT. (a) MIP image shows intense FDG uptake in the right hemithorax along with multiple avid foci in the skeleton (arrows). (b,c) CT reveals a soft tissue mass causing lytic destruction of the adjacent rib(arrow)showingintense FDG uptake on PET(arrows). (d,e) CT shows a lytic lesion in the right ischial tuberosity showing FDG avidity on PET (arrowheads). Biochemical and marrow work up suggested multiple myeloma

Click here to view

   Flurodeoxyglucose Positron Emission Tomography/Computerized Tomography in Predicting Histological Grade and Prognosis Top

Bone and STS are heterogeneous tumors with the histology ranging from low grade to high grade. Within the same tumor, there could be separate foci of high and low grade as well as areas of necrosis. Hence, the histological grading is highly dependent on obtaining an adequate biopsy from the most biologically representative portion of the tumor. Metabolic activity on PET/CT has been correlated with histopathological characteristics of bone and STS and there appears to be a linear relationship with rising grades showing progressively higher SUV[52] [Figure 23]. Chondrosarcomas which show a relatively poor concentration of FDG as compared to other bone and STS also demonstrate increasing metabolism with higher tumor grade.[53] Tumors with myxoid component also tend to show on an average lower SUV values,[54] due to the inability of FDG to access metabolically active cells as they are trapped within a myxoid stroma.[55] Due to the presence of varying tumor features such as poor cellularity, myxoid stroma, necrosis, and hemorrhage, it is important to target the biopsy from the biologically most representative portion of the mass. Biopsy can be directed from the metabolically active component of the tumor seen on PET to obtain a representative tissue sample that shows the correct tumor grade.
Figure 23: 61 man with liposarcoma of the thigh, underwent staging FDG PET/CT.(a) Coronal MIP image shows low grade uptake in the left thigh (arrow). (b) Axial CT shows a mass lesion in the posterior compartment of the thigh predominantly containing fatty tissue (arrow) interspersed with nodular and linear areas of soft tissue attenuation (arrowhead). (c) PET/CT shows low grade FDG uptake in the areas of soft tissue attenuation. Histopathological diagnosis was low grade, well differentiated liposarcoma. 32yr old man with synovial sarcoma of the thigh, underwent staging with FDG PET/CT.(d) MIP image shows intense FDG uptake in the left thigh (arrow). (e) Axial CT shows a soft tissue mass in the posterior compartment of the thigh (arrow). (f) PET/CT image shows intense FDG uptake in lesion. Histopathology revealed high grade synovial sarcoma. FDG uptake correlates with pathological tumor grade with high grade tumors displaying higher tracer concentration and SUV compared to low grade ones

Click here to view

In sarcomas of the bone and soft tissue, the intensity of FDG uptake as measured by the SUV is associated with disease outcome. Tumors with higher SUV are generally high grade and have poorer overall survival compared to those with lower SUV.[56] Thus, FDG PET/CT at diagnosis acts as a very useful predictive tool in these tumors.

   Flurodeoxyglucose Positron Emission Tomography/Computerized Tomography in Evaluation of Treatment Response Top

Bone sarcomas are treated with multimodality treatment that includes chemotherapy, surgery, and radiation. Neoadjuvant chemotherapy downsizes the primary tumor to achieve better local control and also treats micrometastases. Tumor necrosis induced by neoadjuvant chemotherapy is the most important prognostic indicator of survival in patients with localized disease.[57],[58] Histopathological response assessment can only be done on the specimen obtained after surgery. Imaging techniques can act as noninvasive surrogate markers to predict pathological response. Size-based morphologic assessment evaluated by CT and MRI show minimal change despite significant reduction in tumor viability. Since FDG PET is based on glucose metabolism, changes in tumor viability can become evident much earlier compared to morphological assessment. Several studies have evaluated the role of FDG PET/CT is assessing response to chemotherapy in bone sarcomas. These studies have shown the metabolic response measured as changes in SUV of the primary tumor is a fairly accurate predictor of pathological response and tumor necrosis [Figure 24].[59],[60] Metabolic response to chemotherapy seen on FDG PET also correlates with prognosis and survival, with metabolic responders having better outcome compared to metabolic nonresponders.[61] Thus, FDG PET/CT can be potentially used as a noninvasive surrogate marker to predict pathological response as well for prognostication in patients of localized OS and EWS after chemotherapy.
Figure 24: a-b: 21/M with OGS of the femur evaluated with FDG PET/CT at baseline and after 3 cycles of neoadjuvant chemotherapy show significant reduction in FDG uptake at the primary site suggesting metabolic response. Histopathological necrosis of 90% was seen after surgery. c-d: 18/F with tibial OGS evaluated with FDG PET/CT at baseline and after neoadjuvant chemotherapy show no significant change in FDG uptake suggesting metabolic non-responder. Histopathological necrosis of 20 % was seen after surgery

Click here to view

   Pitfalls and False Positives Top

Infection and inflammations affecting various organs of the body including the musculoskeletal system concentrate FDG. One of the proposed mechanisms explaining FDG uptake in inflammatory cells is the overexpression of GLUT-1 subtype receptors in activated macrophages, neutrophils, and lymphocytes. This is the primary cause of FDG uptake in osteomyelitis [Figure 25].[62],[63] Likewise, FDG is known to concentrate in inflammatory arthritis, fractures, healing bone, and recent postsurgical changes.[64] Pelvic insufficiency fractures post radiation therapy for malignancies of the pelvic organs also demonstrate varying intensities of FDG uptake.[65] FDG uptake in these conditions can be a potential cause of false-positive result when FDG PET/CT is performed for an oncologic indication. Correlating the pattern of FDG uptake with clinical symptoms and treatment history along with knowledge of CT features of infection can help diagnose infections and inflammations and avoid potential diagnostic pitfalls.
Figure 25: 64 yr old lady with backache, cough and weight loss underwent FDG PET/CT (a) CT shows an lytic lesion in the right iliac bone (arrow) with an associatedcollection (arrowhead). (b) FDG PET/CT shows increased FDG uptake in the lytic area (arrow) and low grade uptake in the walls of the collection (arrowhead). (c) CT chest shows multiple cavitatory lesions (arrows) in the lungs. Diagnosis of multifocal TB (bone and lungs) was confirmed after growth of acid fast bacilli from the caseous aspirate

Click here to view

Variations in physiological FDG uptake in muscles and bones can occasionally be confusing and simulate disease. Asymmetric physiological uptake in muscles of the head-neck region such as the masseter, pterygoid, and paraspinal muscles can mimic pathology.[66] Excessive muscle activity due to coughing, abnormal muscular strain due to asymmetric weight bearing or a painful condition can also give rise to increased physiological FDG uptake.[67] Focal areas of increased FDG avidity due to red marrow reconversion after administration of marrow stimulating agents is a common cause of abnormal appearing physiological bone uptake.[68] Focal physiological uptake in the region of the growth plate and near tendons attachment of muscles can lead to an erroneous diagnosis.[69] Awareness of these variable patterns of physiological uptake and knowledge of their causative factors is important to avoid potential diagnostic errors.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

   References Top

Johnston J. Giant cell tumor of bone: The role of the giant cell in orthopaedic pathology. Orthop Clin North Am 1977;8:751-70.  Back to cited text no. 1
Ling L, Klein MJ, Sissons HA, Steiner GC, Winchester RJ. Expression of IA and monocyte-macrophage lineage antigens in giant cell tumor of bone and related lesions. Arch Pathol Lab Med 1988;112:65-9.  Back to cited text no. 2
Mészáros K, Lang CH, Bagby GJ, Spitzer JJ. Contribution of different organs to increased glucose consumption after endotoxin administration. J Biol Chem 1987;262:10965-70.  Back to cited text no. 3
Gamelli RL, Liu H, He LK, Hofmann CA. Augmentations of glucose uptake and glucose transporter-1 in macrophages following thermal injury and sepsis in mice. J Leukoc Biol 1996;59:639-47.  Back to cited text no. 4
Schulte M, Brecht-Krauss D, Heymer B, Guhlmann A, Hartwig E, Sarkar MR, et al. Grading of tumors and tumorlike lesions of bone: Evaluation by FDG PET. J Nucl Med 2000;41:1695-701.  Back to cited text no. 5
Aoki J, Watanabe H, Shinozaki T, Takagishi K, Ishijima H, Oya N, et al. FDG PET of primary benign and malignant bone tumors: Standardized uptake value in 52 lesions. Radiology 2001;219:774-7.  Back to cited text no. 6
Shin DS, Shon OJ, Han DS, Choi JH, Chun KA, Cho IH. The clinical efficacy of 18F-FDG-PET/CTin benign and malignant musculoskeletal tumors. Ann Nucl Med 2008;22:603-9.  Back to cited text no. 7
Hermoye A, Malghem J, Lecouvet F, Goffin E, Lonneux M, Lhommel R. F-18 FDG PET/CT as a noninvasive diagnostic and follow-up tool in browntumors due to secondary hyper-parathyroidism. Clin Nucl Med 2009;34:330-2.  Back to cited text no. 8
Lim CH, Park YH, Lee SY, Chung SK. F-18 FDG uptake in the nidus of an osteoid osteoma. Clin Nucl Med 2007;32:628-30.  Back to cited text no. 9
Mungo DV, Zhang X, O'Keefe RJ, Rosier RN, Puzas JE, Schwarz EM. COX-1 and COX-2 expression in osteoid osteomas. J Orthop Res 2002;20:159-62.  Back to cited text no. 10
Purandare NC, Rangarajan V, Shah SA, Sharma AR, Kulkarni SS, Kulkarni AV, et al. Therapeutic response to radiofrequency ablation of neoplastic lesions: FDG PET/CT findings. Radiographics 2011;31:201-13.  Back to cited text no. 11
Rosenthal DI, Hornicek FJ, Torriani M, Gebhardt MC, Mankin HJ. Osteoid osteoma: Percutaneous treatment with radiofrequency energy. Radiology 2003;229:171-5.  Back to cited text no. 12
Petsas T, Megas P, Papathanassiou Z. Radiofrequency ablation of two femoral head chondroblastomas. Eur J Radiol 2007;63:63-7.  Back to cited text no. 13
Martel Villagrán J, Bueno Horcajadas A, Ortiz CruzEJ. Percutaneous radiofrequency ablation of benignbone tumors: Osteoid osteoma, osteoblastoma, andchondroblastoma [in Spanish]. Radiologia 2009;51:549-58.  Back to cited text no. 14
Dahlin DC, Unni KK. Bone Tumors: Generalaspects and Data on 8,542 Cases. 4th ed. Springfield, Ill: Thomas; 1986. p. 413-20.  Back to cited text no. 15
Kubota K, Kubota R, Yamada S. FDG accumulationin tumor tissue. J Nucl Med 1993;34:419-21.  Back to cited text no. 16
Costelloe CM, Chuang HH, Chasen BA, Pan T, Fox PS, Bassett RL, et al. Bone windows for distinguishing malignant from benign primary bone tumors on FDG PET/CT. J Cancer 2013;4:524-30.  Back to cited text no. 17
Feldman F, Heertum RV, Saxena C, Parisien M. 18 F-FDG PET applications for cartilage neoplasms. Skeletal Radiol 2005;34:367-74.  Back to cited text no. 18
Lee FY, Yu J, Chang SS, Fawwaz R, Parisien MV. Diagnostic value and limitations of fluorine-18 fluorodeoxyglucose positron emission tomography for cartilaginous tumors of bone. J Bone Joint Surg Am 2004;86:2677-85.  Back to cited text no. 19
Tsuchiya T, Osanai T, Ishikawa A, Kato N, Watanabe Y, Ogino T. Hibernomas show intense accumulation of FDG positron emission tomography. J Comput Assist Tomogr 2006;30:333-6.  Back to cited text no. 20
Smith CS, Teruya-Feldstein J, Caravelli JF, Yeung HW. False-positive findings on 18F-FDG PET/CT: Differentiation of hibernoma and malignant fatty tumor on the basis of fluctuating standardized uptake values. AJR Am J Roentgenol 2008;190:1091-6.  Back to cited text no. 21
Daigeler A, Vogt PM, Busch K, Pennekamp W, Weyhe D, Lehnhardt M, et al. Elastofibromadorsi – Differentialdiagnosis in chest wall tumours. World J Surg Oncol 2007;5:15.  Back to cited text no. 22
Onishi Y, Kitajima K, Senda M, Sakamoto S, Suzuki K, Maeda T, et al. FDG-PET/CT imaging of elastofibromadorsi. Skeletal Radiol 2011;40:849-53.  Back to cited text no. 23
Fang N, Wang YL, Zeng L, Wu ZJ, Cui XJ, Wang Q, et al. Characteristics of elastofibroma dorsi on PET/CT imaging with (18) F-FDG. Clin Imaging 2016;40:110-3.  Back to cited text no. 24
Järvi OH, Saxén AE, Hopsu-Havu VK, Wartiovaara JJ, Vaissalo VT. Elastofibroma – A degenerative pseudotumor. Cancer 1969;23:42-63.  Back to cited text no. 25
Battaglia M, Vanel D, Pollastri P, Balladelli A, Alberghini M, Staals EL, et al. Imaging patterns in elastofibromadorsi. Eur J Radiol 2009;72:16-21.  Back to cited text no. 26
Davidson T, Goshen E, Eshed I, Goldstein J, Chikman B, Ben-Haim S. Incidental detection of elastofibromadorsi on PET-CT: Initial findings and changes in tumorsize and standardized uptake value on serial scans. Nucl Med Commun 2016;37:837-42.  Back to cited text no. 27
Ogose A, Hotta T, Morita T, Yamamura S, Hosaka N, Kobayashi H, et al. Tumors of peripheral nerves: Correlation of symptoms, clinical signs, imaging features, and histologic diagnosis. Skeletal Radiol 1999;28:183-8.  Back to cited text no. 28
Beaulieu S, Rubin B, Djang D, Conrad E, Turcotte E, Eary JF. Positron emissiontomography of schwannomas: Emphasizing its potential in preoperativeplanning. Am J Roentgenol 2004;182:971-4.  Back to cited text no. 29
Benz MR, Czernin J, Dry SM, Tap WD, Allen-Auerbach MS, Elashoff D, et al. Quantitative F18-fluorodeoxyglucose positron emission tomography accurately characterizes peripheral nerve sheath tumors as malignant or benign. Cancer 2010;116:451-8.  Back to cited text no. 30
Phillips M, Allen C, Gerson P, McClain K. Comparison of FDG-PET scans to conventional radiography and bone scans in management of Langerhans cell histiocytosis. Pediatr Blood Cancer 2009;52:97-101.  Back to cited text no. 31
Feldman F, Vanheertum R, Saxena C. 18Fluoro-deoxyglucose positron emission tomography evaluation of benign versus malignant osteochondromas: Preliminaryobservations. J Comput Assist Tomogr 2006;30:858-64.  Back to cited text no. 32
Purandare NC, Rangarajan V, Agarwal M, Sharma AR, Shah S, Arora A, et al. Integrated PET/CT in evaluating sarcomatous transformation in osteochondromas. Clin Nucl Med 2009;34:350-4.  Back to cited text no. 33
Fisher MJ, Basu S, Dombi E, Yu JQ, Widemann BC, Pollock AN, et al. The role of [18F]-fluorodeoxyglucose positron emissiontomography in predicting plexiform neurofibroma progression. J Neurooncol 2008;87:165-71.  Back to cited text no. 34
Karabatsou K, Kiehl TR, Wilson DM, Hendler A, Guha A. Potential role of 18fluorodeoxyglucose-positron emission tomography/computed tomography indifferentiating benign neurofibroma from malignant peripheral nerve sheath tumor associated with neurofibromatosis 1. Neurosurgery 2009;65 4 Suppl: A160-70.  Back to cited text no. 35
Chirindel A, Chaudhry M, Blakeley JO, Wahl R. 18F-FDG PET/CT qualitative and quantitative evaluation in neurofibromatosis type 1 patients for detection ofmalignant transformation: Comparison of early to delayed imaging with and withoutliver activity normalization. J Nucl Med 2015;56:379-85.  Back to cited text no. 36
Anderson DC. Paget's disease of bone is characterized by excessive bone resorption coupled with excessive and disorganized bone formation. Bone 2001;29:292-3.  Back to cited text no. 37
Cook GJ, Maisey MN, Fogelman I. Fluorine-18-FDG PET in Paget's disease of bone. J Nucl Med 1997;38:1495-7.  Back to cited text no. 38
Völker T, Denecke T, Steffen I, Misch D, Schönberger S, Plotkin M, et al. Positron emission tomographyfor staging of pediatric sarcoma patients: Results of a prospective multicenter trial. J Clin Oncol 2007;25:5435-41.  Back to cited text no. 39
Kneisl JS, Patt JC, Johnson JC, Zuger JH. Is PET useful in detecting occult nonpulmonary metastases in pediatric bone sarcomas? Clin Orthop Relat Res 2006;450:101-4.  Back to cited text no. 40
Newman EN, Jones RL, Hawkins DS. An evaluation of [F-18]-fluorodeoxy-D-glucose positron emission tomography, bone scan, and bone marrow aspiration/biopsy as staging investigations in Ewing sarcoma. Pediatr Blood Cancer 2013;60:1113-7.  Back to cited text no. 41
Byun BH, Kong CB, Lim I, Kim BI, Choi CW, Song WS, et al. Comparison of (18) F-FDG PET/CT and (99 m) Tc-MDP bone scintigraphy for detection of bone metastasis in osteosarcoma. Skeletal Radiol 2013;42:1673-81.  Back to cited text no. 42
Hurley C, McCarville MB, Shulkin BL, Mao S, Wu J, Navid F, et al. Comparison of (18) F-FDG-PET-CT and bone scintigraphy for evaluation of osseous metastases in newly diagnosed and recurrent osteosarcoma. Pediatr Blood Cancer 2016;63:1381-6.  Back to cited text no. 43
Roberge D, Vakilian S, Alabed YZ, Turcotte RE, Freeman CR, Hickeson M. FDG PET/CT in initial staging of adult soft-tissue sarcoma. Sarcoma 2012;2012:960194.  Back to cited text no. 44
Rodeberg D, Paidas C. Childhood rhabdomyosarcoma. Semin Pediatr Surg 2006;15:57-62.  Back to cited text no. 45
Tateishi U, Hosono A, Makimoto A, Nakamoto Y, Kaneta T, Fukuda H, et al. Comparative study of FDG PET/CT andconventional imaging in the staging of rhabdomyosarcoma. Ann Nucl Med 2009;23:155-61.  Back to cited text no. 46
Norman G, Fayter D, Lewis-Light K, Chisholm J, McHugh K, Levine D, et al. An emerging evidence base for PET-CT in the management of childhood rhabdomyosarcoma: Systematic review. BMJ Open 2015;5:e006030.  Back to cited text no. 47
Fouquet G, Guidez S, Herbaux C, Van de Wyngaert Z, Bonnet S, Beauvais D, et al. Impact of initial FDG-PET/CT and serum-free light chain on transformation of conventionally defined solitary plasmacytoma to multiple myeloma. Clin Cancer Res 2014;20:3254-60.  Back to cited text no. 48
Salaun PY, Gastinne T, Frampas E, Bodet-Milin C, Moreau P, Bodéré-Kraeber F. FDG-positron-emission tomography for staging and therapeutic assessment in patients with plasmacytoma. Haematologica 2008;93:1269-71.  Back to cited text no. 49
Bailly C, Leforestier R, Jamet B, Carlier T, Bourgeois M, Guérard F, et al. PET imaging for initial staging and therapy assessment in multiple myeloma patients. Int J Mol Sci 2017;18:E445.  Back to cited text no. 50
Siontis B, Kumar S, Dispenzieri A, Drake MT, Lacy MQ, Buadi F, et al. Positron emission tomography-computed tomography in the diagnostic evaluation of smoldering multiple myeloma: Identification of patients needing therapy. Blood Cancer J 2015;5:e364.  Back to cited text no. 51
Rakheja R, Makis W, Skamene S, Nahal A, Brimo F, Azoulay L, et al. Correlating metabolic activity on 18F-FDG PET/CT with histopathologic characteristics of osseous and soft-tissue sarcomas: A retrospective review of 136 patients. AJR Am J Roentgenol 2012;198:1409-16.  Back to cited text no. 52
Brenner W, Conrad EU, Eary JF. FDG PET imaging for grading and prediction of outcome in chondrosarcoma patients. Eur J Nucl Med Mol Imaging 2004;31:189-95.  Back to cited text no. 53
Sheah K, Ouellette HA, Torriani M, Nielsen GP, Kattapuram S, Bredella MA. Metastatic myxoid liposarcomas: Imaging and histopathologic findings. Skeletal Radiol 2008;37:251-8.  Back to cited text no. 54
Schwab JH, Healey JH. FDG-PET lacks sufficient sensitivity to detect myxoid liposarcoma spinal metastases detected by MRI. Sarcoma 2007;2007:36785.  Back to cited text no. 55
Kubo T, Furuta T, Johan MP, Ochi M. Prognostic significance of (18) F-FDG PET at diagnosis in patients with soft tissue sarcoma and bone sarcoma; systematic review and meta-analysis. Eur J Cancer 2016;58:104-11.  Back to cited text no. 56
Picci P, Böhling T, Bacci G, Ferrari S, Sangiorgi L, Mercuri M, et al. Chemotherapy-induced tumor necrosis as a prognostic factor in localized Ewing's sarcoma of the extremities. J Clin Oncol 1997;15:1553-9.  Back to cited text no. 57
Davis AM, Bell RS, Goodwin PJ. Prognostic factors in osteosarcoma: A critical review. J Clin Oncol 1994;12:423-31.  Back to cited text no. 58
Franzius C, Sciuk J, Brinkschmidt C, Jürgens H, Schober O. Evaluation of chemotherapy response in primary bone tumors with F-18 FDG positron emission tomography compared with histologically assessed tumor necrosis. Clin Nucl Med 2000;25:874-81.  Back to cited text no. 59
Hawkins DS, Rajendran JG, Conrad EU 3rd, Bruckner JD, Eary JF. Evaluation of chemotherapy response in pediatric bone sarcomas by [F-18]-fluorodeoxy- D-glucose positron emission tomography. Cancer 2002;94:3277-84.  Back to cited text no. 60
Hawkins DS, Schuetze SM, Butrynski JE, Rajendran JG, Vernon CB, Conrad EU 3rd, et al. Fluorodeoxyglucose positron emission tomography predicts outcome for Ewing sarcoma family of tumors. J Clin Oncol 2005;23:8828-34.  Back to cited text no. 61
Guhlmann A, Brecht-Krauss D, Suger G, Glatting G, Kotzerke J, Kinzl L, et al. Chronic osteomyelitis: Detection with FDG PET and correlation with histopathologic findings. Radiology 1998;206:749-54.  Back to cited text no. 62
Sugawara Y, Braun DK, Kison PV, Russo JE, Zasadny KR, Wahl RL. Rapid detection of human infections with fluorine-18 fluorodeoxyglucose and positron emission tomography: Preliminary results. Eur J Nucl Med 1998;25:1238-43.  Back to cited text no. 63
Zhuang H, Sam JW, Chacko TK, Duarte PS, Hickeson M, Feng Q, et al. Rapid normalization of osseous FDG uptake following traumatic or surgical fractures. Eur J Nucl Med Mol Imaging 2003;30:1096-103.  Back to cited text no. 64
Long NM, Smith CS. Causes and imaging features of false positives and false negatives on F-PET/CT in oncologic imaging. Insights Imaging 2011;2:679-98.  Back to cited text no. 65
Blodgett TM, Fukui MB, Snyderman CH, Branstetter BF 4th, McCook BM, Townsend DW, et al. Combined PET-CT in the head and neck: part 1. Physiologic, altered physiologic, and artifactual FDG uptake. Radiographics 2005;25:897-912.  Back to cited text no. 66
Jackson RS, Schlarman TC, Hubble WL, Osman MM. Prevalence and patterns of physiologic muscle uptake detected with whole-body 18F-FDG PET. J Nucl Med Technol 2006;34:29-33.  Back to cited text no. 67
Okuyama C, Sasaki N, Nishimura M, Matsushima S, Yoshimatsu R. Active bone marrow with focal FDG accumulation mimicking bone metastasis with a case of early esophageal cancer. Clin Nucl Med 2018;43:258-61.  Back to cited text no. 68
Sopov V, Bernstine H, Stern D, Yefremov N, Sosna J, Groshar D. Spectrum of focal benign musculoskeletal 18F-FDG uptake at PET/CT of the shoulder and pelvis. AJR Am J Roentgenol 2009;192:1029-35.  Back to cited text no. 69


  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8], [Figure 9], [Figure 10], [Figure 11], [Figure 12], [Figure 13], [Figure 14], [Figure 15], [Figure 16], [Figure 17], [Figure 18], [Figure 19], [Figure 20], [Figure 21], [Figure 22], [Figure 23], [Figure 24], [Figure 25]

  [Table 1]


    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

  In this article
    Prediction of Ma...
    Pitfalls and Fal...
    Benign Soft-Tiss...
    Benign Bone Lesi...
    Article Figures
    Article Tables

 Article Access Statistics
    PDF Downloaded49    
    Comments [Add]    

Recommend this journal