DOI: 10.1148/rg.273065031
RadioGraphics 2007;27:805-826
© RSNA, 2007
Pitfalls in MR Image Interpretation Prompting Referrals to an Orthopedic Oncology Clinic1
Gregory Scott Stacy, MD and
Larry B. Dixon, MD
1 From the Department of Radiology, University of Chicago Hospitals, 5841 S Maryland Ave, MC 2026, Chicago, IL 60637. Recipient of a Certificate of Merit award for an education exhibit at the 2005 RSNA Annual Meeting. Received March 17, 2006; revision requested August 14 and received August 25; accepted August 28. Authors have no financial relationships to disclose.
Address correspondence to G.S.S. (e-mail: sstacy{at}radiology.bsd.uchicago.edu).
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Abstract
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Patients referred to the authors hospital for evaluation on suspicion of a bone or soft-tissue malignancy frequently present to the Orthopaedic Oncology Clinic with magnetic resonance (MR) images that show typical features of nonmalignant or nonneoplastic entities. The purpose of this article is to review the benign entities that may be mistaken by the radiologist for a malignancy and thus lead to needless referral to an orthopedic oncologist. Normal hematopoietic marrow and marrow edema due to a stress reaction may mimic a neoplasm at MR imaging, but knowledge of the typical patterns and locations of these features allows an accurate radiologic interpretation. The MR imaging appearance of osteonecrosis, Paget disease, benign bone lesions, and rheumatologic conditions may be confusing; in such circumstances, radiographic findings may help formulate a correct diagnosis. Knowledge of the common locations and appearances of bursae and ganglia is necessary so that radiologists do not misinterpret these benign entities as soft-tissue sarcomas. Soft-tissue trauma and inflammation also may mimic tumors at MR imaging, but a familiarity with the imaging patterns of nonneoplastic change in muscle allows the avoidance of misinterpretation. The clinical history, as always, is an important component of proper diagnosis. The radiologist can be especially useful to both the clinician and the patient by recognizing entities that are highly unlikely to represent malignancy and by confidently reporting those entities as benign, thereby sparing the patient an unnecessary trip to the orthopedic oncologist.
© RSNA, 2007
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LEARNING OBJECTIVES FOR TEST 4
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After reading this article and taking the test, the reader will be able to:
- Recognize the importance of accurate radiologic interpretation of benign and nonneoplastic entities to avoid unnecessary referrals to an orthopedic oncologist.
- Describe the MR imaging features of nonneoplastic or benign marrow, articular, and soft-tissue processes that may mimic malignancy but that do not require referral to an orthopedic oncologist.
- Identify the MR imaging features specific to marrow, articular, and soft-tissues processes that warrant referral to an orthopedic oncologist.
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Introduction
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The orthopedic oncology team at our hospital includes surgeons, oncologists, pathologists, and radiologists who specialize in the diagnosis and treatment of tumors of bone and soft tissue. As the radiologists on this team, we are fortunate to be able to attend the Orthopaedic Oncology Clinic, where the surgeons see both new and returning patients. Most of the new patients are referred to the clinic from another institution, and they are asked to provide all pertinent imaging studies performed at the referring institution. We review these images with the orthopedic surgeons to decide whether the lesion truly represents a neoplasm that requires further work-up and possibly treatment. New patients also are asked to provide for our review the reports of imaging studies performed at the referring hospitals and clinics. While reviewing these reports, we noticed that radiologists often misinterpreted certain imaging patterns and nonneoplastic disease entities as representative of a possible malignancy (Table 1).
Over a 12-month period, 390 patients presented to the Orthopaedic Oncology Clinic at our institution with recently discovered imaging abnormalities interpreted by radiologists at the referring institutions as possibly representative of a neoplasm, findings that directly or indirectly resulted in the patients referral to our clinic. These patients did not have a biopsy-based diagnosis when they presented to the clinic. Approximately two-thirds of them had undergone imaging with subsequent findings indicative of an entity that required follow-up and possibly treatment (Table 2). Each of these entities was initially interpreted by the radiologist at the referring institution as a tumor or potential tumor; hence, these patients were appropriately referred to the clinic, even if the initial diagnosis did not match the subsequent consensus diagnosis by our orthopedic oncology team. The remaining one-third of the patients who were referred to the clinic had images with features that, in the opinion of the orthopedic oncology team, were clearly characteristic either of nonneoplastic entities or of benign tumors that did not require follow-up or treatment by an orthopedic oncologist. The entities that most commonly did not require follow-up by an orthopedic oncologist are the focus of this article. We have limited the detailed discussion to entities that were observed in at least five patients referred to our clinic during the 12-month period. We have classified these entities into three groups: marrow pitfalls, articular and juxta-articular pitfalls, and soft-tissue pitfalls.
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Marrow Pitfalls
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Normal Hematopoietic Marrow
The marrow cavity of the skeleton contains both fat cells and hematopoietic cells. When the hematopoietic elements predominate, the marrow is described as "red"; in "yellow" marrow, the fatty element predominates. The appendicular skeleton undergoes an orderly but variable conversion from predominantly red marrow at birth to yellow marrow (1,2). Within an extremity, conversion occurs earlier in the distal bones than in the proximal bones. Within a given long bone, the conversion occurs first in the epiphyses and apophyses, next in the diaphysis, and finally in the metaphyses; conversion also generally occurs first centrally and later peripherally (ie, subcortically) within the marrow.
On T1-weighted magnetic resonance (MR) images, the signal intensity of normal yellow marrow is like that of subcutaneous fat. Yellow marrow appears darker on MR images obtained with fat suppression. On T1-weighted MR images, the signal intensity of normal red marrow is lower than that of fat (and, hence, of yellow marrow) but generally higher than that of skeletal muscle because of an admixture of fatty elements with hematopoietic elements. On T2-weighted fat-suppressed MR images, the signal intensity of normal red marrow is higher than that of yellow marrow and often is similar to or slightly higher than that of skeletal muscle.
"Residual" red marrow is a typical component of the bones of the axial skeleton and frequently is present in the proximal metaphyses of the femora and humeri in normal adults (3). Residual red marrow is symmetric in distribution, and hence its observation in both proximal femora at pelvic MR imaging does not usually cause any diagnostic confusion. However, if one of the two extremities is unavailable for comparison, the nonfatty signal of residual red marrow may be mistaken for that of a neoplasm. Residual red marrow is seen fairly often in the distal femur at MR imaging of the knee (4), particularly in adolescents and women of menstruating age. Red marrow may persist in a focal, geographic, patchy pattern that occasionally mimics an intramedullary lesion (Fig 1). Knowledge of the typical distribution of residual red marrow in adults and the signal characteristics of normal red marrow should allow the avoidance of misdiagnosis.

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Figure 1a. Normal hematopoietic (or red) marrow in a 21-year-old woman with knee pain and no additional medical problems. (a) Coronal T1-weighted MR image shows patchy regions of intermediate signal intensity (arrows) in the distal femur. These regions have signal intensity higher than that in nearby skeletal muscle (*), and this characteristic is suggestive of residual red marrow. (b) Coronal T2-weighted fat-suppressed MR image shows a patchy area (arrow) with signal intensity similar to that of skeletal muscle (*). MR images from 1%2% of patients referred to the Orthopaedic Oncology Clinic showed similar features that are characteristic of residual red marrow but that were misinterpreted as potential malignancy.
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Figure 1b. Normal hematopoietic (or red) marrow in a 21-year-old woman with knee pain and no additional medical problems. (a) Coronal T1-weighted MR image shows patchy regions of intermediate signal intensity (arrows) in the distal femur. These regions have signal intensity higher than that in nearby skeletal muscle (*), and this characteristic is suggestive of residual red marrow. (b) Coronal T2-weighted fat-suppressed MR image shows a patchy area (arrow) with signal intensity similar to that of skeletal muscle (*). MR images from 1%2% of patients referred to the Orthopaedic Oncology Clinic showed similar features that are characteristic of residual red marrow but that were misinterpreted as potential malignancy.
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Yellow marrow may revert to red marrow if there is an increased hematopoietic demand. In the chronically ill, including those with myeloproliferative disorders, the signal of red marrow may appear isointense or even hypointense to that of skeletal muscle on T1-weighted images. The distribution of reverted red marrow and marrow affected by myeloproliferative disease tends to be symmetric. Imaging of the contralateral extremity therefore may be useful in certain cases.
Osteoid osteomas and stress fractures in the cortex may lead to edema in the adjacent marrow that may mimic the patchy pattern of normal hematopoietic red marrow on MR images; hence, careful evaluation of the cortex is recommended in cases where peripheral nonfatty marrow is evident.
Stress Fractures and Stress Reaction
Bone marrow edema may result from a variety of nonneoplastic disorders. In some cases, an associated abnormality, such as erosion (eg, from rheumatoid arthritis) or an abscess, may be evident. In other cases (eg, in bone contusion, early-stage osteonecrosis, and transient migratory edema), there may be no discrete underlying or adjacent lesion. Stress reaction and stress fracture were the most common causes of nonneoplastic edema seen at MR imaging in patients referred to the Orthopaedic Oncology Clinic.
The detection and interpretation of stress fractures pose challenges to radiologists. The radiographic features of stress fracture vary in accordance with the location and chronicity of the injury and may include periosteal reaction, endosteal sclerosis, cortical thickening, and a lucent fracture line (5). Often radiographs appear normal in the early stages of a fracture.
Even before they can be seen on radiographs, stress fractures often produce marrow edema that is visible at MR imaging. Although such edema may mimic a malignancy, a discrete hypointense fracture line within the area of edema in a patient suspected of having a stress fracture allows an accurate diagnosis (Fig 2). A focus of increased signal intensity in the adjacent cortex also may be visible, particularly in the long bones (6). MR images also may show periosteal and marrow edema, which have been referred to as a "stress reaction," before the development of a discrete hypointense fracture line (7). Initially, the edema may be apparent only on T2-weighted images; however, marrow edema becomes visible also on T1-weighted images as the stress reaction progresses, and a fracture line eventually develops. Adjacent soft-tissue edema and enhancement (Fig 3) may lead the interpreting radiologist to suspect a neoplasm. In some instances, computed tomography (CT) may be necessary to provide the specificity needed to diagnose a stress fracture, particularly in the sacrum (8). Radiologists should be familiar with the common locations of stress injuries (Table 3). Such familiarity is particularly important in cases where the injury is manifested on MR images as edema without a discrete fracture line (9). In our experience, the edema associated with stress fracture and stress reaction is frequently much more pronounced on T2-weighted fat-suppressed images than on T1-weighted images and is often ill defined, particularly on T1-weighted images (Fig 3b); in contrast, a well-defined hypointense rounded lesion is usually evident on T1-weighted images in patients with a neoplasm.

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Figure 2a. Fatigue fracture in a 25-year-old woman runner with low back pain. Coronal T1-weighted (a) and coronal T2-weighted fat-suppressed (b) MR images show edema in the left sacral ala as well as a linear band (arrow) that extends through the region of edema, a typical finding of stress fracture. MR images from nearly 2% of patients referred to the Orthopaedic Oncology Clinic showed features characteristic of stress fracture or stress reaction that were misinterpreted as a potential malignancy.
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Figure 2b. Fatigue fracture in a 25-year-old woman runner with low back pain. Coronal T1-weighted (a) and coronal T2-weighted fat-suppressed (b) MR images show edema in the left sacral ala as well as a linear band (arrow) that extends through the region of edema, a typical finding of stress fracture. MR images from nearly 2% of patients referred to the Orthopaedic Oncology Clinic showed features characteristic of stress fracture or stress reaction that were misinterpreted as a potential malignancy.
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Figure 3a. Metatarsal stress fracture in a 53-year-old woman with forefoot pain. (a) Short-axis T1-weighted fat-suppressed MR image, obtained after the intravenous administration of a gadolinium chelate, shows enhancement of the marrow of the fourth metatarsal (arrowhead) as well as the surrounding soft tissues (arrow). (b) Sagittal T1-weighted MR image shows mild and poorly defined low-signal-intensity edema (arrowhead) in the marrow of the distal fourth metatarsal, with a slight angulation of the dorsal cortex (arrow), findings suggestive of a stress fracture. Follow-up radiographs (not shown) revealed callus formation at the site, a finding that helped confirm the diagnosis. Stress fractures and stress reaction often result in relatively mild marrow edema on T1-weighted images, compared with more pronounced marrow and soft-tissue edema on T2-weighted images. Marrow and soft-tissue enhancement after gadolinium administration also is fairly common.
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Figure 3b. Metatarsal stress fracture in a 53-year-old woman with forefoot pain. (a) Short-axis T1-weighted fat-suppressed MR image, obtained after the intravenous administration of a gadolinium chelate, shows enhancement of the marrow of the fourth metatarsal (arrowhead) as well as the surrounding soft tissues (arrow). (b) Sagittal T1-weighted MR image shows mild and poorly defined low-signal-intensity edema (arrowhead) in the marrow of the distal fourth metatarsal, with a slight angulation of the dorsal cortex (arrow), findings suggestive of a stress fracture. Follow-up radiographs (not shown) revealed callus formation at the site, a finding that helped confirm the diagnosis. Stress fractures and stress reaction often result in relatively mild marrow edema on T1-weighted images, compared with more pronounced marrow and soft-tissue edema on T2-weighted images. Marrow and soft-tissue enhancement after gadolinium administration also is fairly common.
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Osteonecrosis
Osteonecrosis refers to changes that occur in bone as a result of ischemia. The many possible causes of osteonecrosis include trauma, hemoglobinopathies (eg, sickle cell disease), vasculitides (eg, lupus erythematosus), and medical treatments (eg, corticosteroid therapy) (10).
Osteonecrosis that occurs in subarticular locations (eg, in the femoral head) is easily recognized by most radiologists. Metadiaphyseal osteonecrosis, on the other hand, has received relatively little attention in the radiology literature and is more likely to be a source of uncertainty for radiologists, judging from the radiologic reports of imaging studies in patients referred to our clinic. The characteristic radiographic pattern of metadiaphyseal osteonecrosis is that of a serpentine ringlike band of sclerosis that separates a central necrotic zone of variable lucency from surrounding normal marrow; however, this pattern is a relatively late manifestation of osteonecrosis. Earlier in the course of disease, osteonecrosis may result in a poorly defined region of lucency within the medullary space, a feature that may be indistinguishable from a lytic neoplastic process at radiography (Fig 4) (11,12). In such cases, a correct diagnosis of osteonecrosis often can be rendered easily with the aid of MR imaging.

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Figure 4a. Myelodysplastic syndrome in a 43-year-old woman with ankle pain. (a) Lateral ankle radiograph shows a poorly defined region of lucency (arrowheads) centrally within the distal tibia. (b) Sagittal T1-weighted MR image shows a curvilinear band of low signal intensity (arrowhead) that surrounds a central region of fat signal intensity (*). (c) Sagittal T2-weighted fat-suppressed MR image shows a high-signal-intensity curvilinear band that surrounds a low-signal-intensity central region of necrotic bone. Note the double line sign (arrow), a feature that is virtually pathognomonic of osteonecrosis. Images from 2%3% of patients referred to the Orthopaedic Oncology Clinic showed findings characteristic of osteonecrosis but interpreted as potential malignancy. MR imaging should allow a confident diagnosis in most cases.
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Figure 4b. Myelodysplastic syndrome in a 43-year-old woman with ankle pain. (a) Lateral ankle radiograph shows a poorly defined region of lucency (arrowheads) centrally within the distal tibia. (b) Sagittal T1-weighted MR image shows a curvilinear band of low signal intensity (arrowhead) that surrounds a central region of fat signal intensity (*). (c) Sagittal T2-weighted fat-suppressed MR image shows a high-signal-intensity curvilinear band that surrounds a low-signal-intensity central region of necrotic bone. Note the double line sign (arrow), a feature that is virtually pathognomonic of osteonecrosis. Images from 2%3% of patients referred to the Orthopaedic Oncology Clinic showed findings characteristic of osteonecrosis but interpreted as potential malignancy. MR imaging should allow a confident diagnosis in most cases.
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Figure 4c. Myelodysplastic syndrome in a 43-year-old woman with ankle pain. (a) Lateral ankle radiograph shows a poorly defined region of lucency (arrowheads) centrally within the distal tibia. (b) Sagittal T1-weighted MR image shows a curvilinear band of low signal intensity (arrowhead) that surrounds a central region of fat signal intensity (*). (c) Sagittal T2-weighted fat-suppressed MR image shows a high-signal-intensity curvilinear band that surrounds a low-signal-intensity central region of necrotic bone. Note the double line sign (arrow), a feature that is virtually pathognomonic of osteonecrosis. Images from 2%3% of patients referred to the Orthopaedic Oncology Clinic showed findings characteristic of osteonecrosis but interpreted as potential malignancy. MR imaging should allow a confident diagnosis in most cases.
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On MR images, metadiaphyseal osteonecrosis usually manifests as a well-defined serpentine rim of low signal intensity on T1-weighted images (Fig 4). This feature corresponds to the sclerotic band that may be seen on radiographs but that is occasionally too faint to detect. On T2-weighted MR images, the rim may have low signal intensity, high signal intensity, or both, and a pathognomonic "double line" sign (bands of low and high signal intensity that course together in parallel) often is seen. The signal intensity of marrow inside the rim usually is the same as that of fat but occasionally is heterogeneously hypointense on T1-weighted images because of fibrosis or calcification (10).
One of the earliest MR imaging findings of osteonecrosis is nonspecific marrow edema (13). Marrow edema caused by osteonecrosis may be difficult or impossible to differentiate from marrow edema with other causes, including transient migratory edema. If the edema does not appear to be associated with a discrete lesion and if osteonecrosis is suspected clinically, then follow-up MR imaging may be indicated to monitor the regression of edema or its progression to a pattern more specific to osteonecrosis.
Metadiaphyseal osteonecrosis rarely may undergo sarcomatous degeneration. Such degeneration should be suspected if cortical destruction or a soft-tissue mass is seen (Fig 5). It is appropriate to refer patients with such findings to an orthopedic oncologist.

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Figure 5. Sarcomatous degeneration of bone in a 57-year-old man with right knee pain that did not respond to physical therapy. Anteroposterior radiograph of the knee shows sclerotic lesions typical of multifocal osteonecrosis (arrowheads). Destruction of the lateral cortex of the proximal tibia (arrow) is indicative of sarcomatous degeneration, a finding that was confirmed at MR imaging. This patient was appropriately referred to the Orthopaedic Oncology Clinic.
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Paget Disease
Paget disease of bone is estimated to affect approximately 3% of the population older than 40 years and approximately 10% of the elderly (older than 80 years) (14). It is characterized by abnormal activity of osteoclasts and osteoblasts that leads to the deposition of irregular new bone (15). Paget disease most commonly involves the pelvis but also may affect the remainder of the axial skeleton and the proximal femora.
Paget disease usually produces specific features on radiographs. In long bones, the initial "active" phase of disease manifests as osteolysis that extends from the end of the bone into the diaphysis with a characteristic flame-shaped advancing front. Cortical and trabecular thickening denote an "inactive" phase (14). Both phases may be evident at the same time. Radiologists may be hesitant to offer a diagnosis of Paget disease if the patient is relatively young or if the process is observed in an atypical location (Fig 6).

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Figure 6. Paget disease of bone in a 64-year-old woman. Lateral radiograph of the distal forearm shows the advancing lytic front typical of the "active" phase of disease (arrowhead) and cortical and trabecular thickening characteristic of the "sclerotic" phase (arrow), as well as bowing and generalized expansile remodeling of the distal radius. Patients with images that showed characteristic features of Paget disease in unusual locations (eg, bones of the upper extremity) occasionally were referred to the Orthopaedic Oncology Clinic with a presumptive diagnosis of neoplasm.
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MR imaging usually is not necessary for the diagnosis of Paget disease. The signal intensity of marrow in pagetoid bone is predominantly the same as that of fat; hence, Paget disease may be easily overlooked at MR imaging (15). Moreover, the MR imaging appearance of Paget disease in bone is variable, and this may exacerbate confusion. For example, fibrovascular or sclerotic elements may appear as focal or diffuse intermediate- or low-signal-intensity regions on T1-weighted images (Fig 7), and these features may be misinterpreted as neoplasms (16). Marrow may have increased signal intensity on T2-weighted fat-suppressed images if vascular tissue predominates. In cases of diffuse marrow changes, the presence of small residual fatty foci supports a diagnosis of Paget disease. Evaluation of cortical thickness also is useful; however, the cortical thickening typical in Paget disease may not be as obvious on MR images as on radiographs or CT scans.

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Figure 7a. Paget disease of bone in a 50-year-old woman. (a) Axial T1-weighted MR image of the pelvis shows abnormally low-signal-intensity marrow in the left ilium (arrowhead) and thickened cortex (arrow). (b) Axial CT image of the pelvis better illustrates the cortical thickening (arrow), a finding typical of Paget disease. Approximately 1% of patients referred to the Orthopaedic Oncology Clinic had abnormalities at MR imaging that could have been easily diagnosed as Paget disease at radiography or CT.
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Figure 7b. Paget disease of bone in a 50-year-old woman. (a) Axial T1-weighted MR image of the pelvis shows abnormally low-signal-intensity marrow in the left ilium (arrowhead) and thickened cortex (arrow). (b) Axial CT image of the pelvis better illustrates the cortical thickening (arrow), a finding typical of Paget disease. Approximately 1% of patients referred to the Orthopaedic Oncology Clinic had abnormalities at MR imaging that could have been easily diagnosed as Paget disease at radiography or CT.
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The development of sarcoma within pagetoid bone is a rare but well-described complication (17). In most patients with this complication, a soft-tissue mass is evident on radiographs and MR images. Referral of these patients to an orthopedic oncologist is appropriate.
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Fibroxanthoma (Nonossifying Fibroma) and Other Benign Lesions
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Many patients who were referred to the Orthopaedic Oncology Clinic had benign bone tumors that were correctly diagnosed by radiologists at the referring institution on the basis of typical imaging features. Tumors of this kind are often locally aggressive and require surgery, and therefore the referral of these patients to an orthopedic oncologist is appropriate. However, some of the patients who were referred to the clinic had imaging studies that showed typical "latent" or inactive lesions that were mistaken by radiologists for more aggressive lesions. In the latter group, the most common lesion was fibroxanthoma (nonossifying fibroma).
Fibroxanthomas are common in growing children and generally do not require referral to an orthopedic surgeon unless a fracture is present or the lesion is unusually large. They typically occur in the metadiaphyseal regions of the long bones, most commonly in the lower extremities, and are cortically based or eccentrically positioned within the bone (18). They have a characteristic radiographic appearance and should not be mistaken for a malignancy. The lesions are lucent early in their development, but they maintain well-defined and usually sclerotic margins. A multilocular appearance is typical (Fig 8a), and mild expansile remodeling of the bone may occur. As the lesions mature, sclerotic components develop. Most lesions eventually disappear.

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Figure 8a. Fibroxanthoma (nonossifying fibroma) in a 16-year-old girl. (a) Lateral radiograph of the knee shows a mixed lucent and sclerotic intramedullary lesion (arrowheads) along the posterior cortex of the distal femur. The sclerotic margin and multilocular appearance are typical of a fibroxanthoma. (b) Sagittal T2-weighted MR image of the knee shows areas of heterogeneous signal intensity (arrowheads) within the lesion. Images from 2%3% of patients referred to the Orthopaedic Oncology Clinic showed features characteristic of fibroxanthoma but interpreted as a potential malignancy. Several of these patients arrived with only MR images and probably would not have been referred if a radiograph had been obtained for correlation.
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Figure 8b. Fibroxanthoma (nonossifying fibroma) in a 16-year-old girl. (a) Lateral radiograph of the knee shows a mixed lucent and sclerotic intramedullary lesion (arrowheads) along the posterior cortex of the distal femur. The sclerotic margin and multilocular appearance are typical of a fibroxanthoma. (b) Sagittal T2-weighted MR image of the knee shows areas of heterogeneous signal intensity (arrowheads) within the lesion. Images from 2%3% of patients referred to the Orthopaedic Oncology Clinic showed features characteristic of fibroxanthoma but interpreted as a potential malignancy. Several of these patients arrived with only MR images and probably would not have been referred if a radiograph had been obtained for correlation.
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The MR imaging appearance of fibroxanthomas varies with the developmental stage of the lesion and correlates with the radiographic appearance. The lesion is eccentrically positioned within the bone and typically has hyperintense signal on T2-weighted images early in its development. As the lesion matures, foci of low signal intensity appear that correspond histologically to hypercellular fibrous tissue and hemosiderin deposits (18). Frequently, a combination of high-and low-signal-intensity components is observed (Fig 8b). A peripheral hypointense rim corresponds to marginal sclerosis on radiographs. Adjacent marrow edema is generally absent in uncomplicated lesions.
Occasionally, a fibroxanthoma may be unusually large and may cause so much expansile remodeling that it becomes difficult to distinguish from lesions such as an aneurysmal bone cyst or a chondromyxoid fibroma (19). Referral to an orthopedic oncologist in such cases is reasonable.
Several of the patients referred to our clinic had bone lesions with imaging features characteristic of benign entities that did not require further work-up or treatment. The images depicted classic examples of fibrous dysplasia, intraosseous lipoma, calcaneal solitary bone cyst, vertebral hemangioma, and other lesion types. These entities generally do not require referral to an orthopedic oncologist unless a fracture is present.
Patients with enchondromas were commonly referred to our clinic. Because it may be difficult to distinguish a large enchondroma from a low-grade chondrosarcoma on the basis of imaging features alone (ie, without a precise correlation with clinical symptoms), the referral of such cases to an orthopedic oncologist may be well founded; referral at least allows appropriate examination and follow-up. There were, however, a few cases of small enchondromas of the finger seen on radiographs and small enchondromas with the classic lobular appearance seen on MR images (Fig 9) that were misinterpreted as likely malignancies, and these patients were needlessly referred to the clinic (20).

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Figure 9. Enchondroma in a 40-year-old woman. Coronal T1-weighted MR image of the knee shows a small lobulated lesion (arrow) in the medullary cavity of the proximal tibia, a typical appearance of a benign enchondroma. Patients with a small, painless, lobulated lesion such as this need not be referred to an orthopedic oncologist.
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Articular and Juxta-articular Pitfalls
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Arthritis and Rheumatologic Conditions
True primary intra-articular malignant neoplasms are rare. Processes that result in nonneoplastic soft-tissue abnormalities in and around the joint as well as nonneoplastic subarticular marrow abnormalities are common. Apparent masses in intra-articular and juxta-articular locations may result from synovitis, loose bodies, and a variety of depositional diseases that typically have classic radiographic appearances but potentially confusing MR imaging features. Various rheumatologic conditions also may result in prominent subchondral cysts or erosions, occasionally with adjacent marrow edema, that may mimic a more sinister process at MR imaging.
In our opinion, the key to diagnosing a rheumatologic condition at MR imaging is to search for the same features that would establish the diagnosis at radiography. Does the process result in abnormalities on both sides of the joint? Are multiple joints involved? Is the articular cartilage abnormally thinned, with resultant narrowing of the joint?
Subchondral degenerative cysts are common in patients with osteoarthritis. These cysts can become quite large, particularly those in the femoral head and acetabulum. In our experience, however, such cysts are invariably associated with other features of osteoarthritis, including narrowing of the joint and osteophyte formation; these other features may be more readily appreciated on radiographs than on large-field-of-view MR images. Furthermore, subchondral cysts are often multiple and located on both sides of the joint. Bone proliferation from osteophyte formation, particularly at the sternoclavicular joint, occasionally produces an apparent mass both at physical examination and at MR imaging; CT may help secure the diagnosis of osteoarthritis in such questionable cases.
Synovitis is the hallmark of inflammatory arthritides, and radiologists who are unfamiliar with the MR imaging appearance of a thickened enhancing pannus may mistake it for a tumor. Gadolinium eventually passes from the synovium into the joint fluid, where it may produce enhancement of the entire joint and its contents, enhancement that is suggestive of a solid intra-articular mass. Hence, delayed imaging after gadolinium administration is generally discouraged. Observation of synovitis in other joints or adjacent tendon sheaths supports the diagnosis of inflammatory arthritis. Like degenerative cysts, subchondral erosions in inflammatory arthritis may become quite large, may be surrounded by marrow edema, and occasionally may mimic a tumor. The presence of multiple subchondral lesions with accompanying synovitis in a joint, or the involvement of multiple joints, opposes a diagnosis of malignancy (Fig 10).

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Figure 10. Rheumatoid arthritis in a 61-year-old man. Coronal T2-weighted fat-suppressed image of the ankle shows a high-signal-intensity lesion with a surrounding hypointense rim (large arrow) in the inferior aspect of the talar body, features that represent an area of subcortical erosion with adjacent bone marrow edema. Several smaller areas of erosion in the calcaneus (small arrows) and high-signal-intensity synovitis in the tarsal sinus (*) support a diagnosis of erosive inflammatory arthritis rather than a neoplasm. Subchondral erosions and degenerative cysts, particularly larger (13-cm) lesions with adjacent edema and enhancement, were commonly misinterpreted as a neoplasm and resulted in needless referrals to the Orthopaedic Oncology Clinic. This case demonstrates the importance of recognizing an arthritic process.
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Tophaceous gout, particularly in the hands and feet, may appear on MR images as an intra-articular or periarticular mass mimicking a tumor. However, gouty tophi, unlike most soft-tissue sarcomas, often have intermediate to low signal intensity on T2-weighted images (21). The radiographic features of goutmainly calcification of tophi and marginal erosion of the adjacent bonemay be more familiar to radiologists. Apart from the tophi and bone erosion, features that may be depicted as areas of low signal intensity on T2-weighted MR images include intra-articular amyloid deposits, rice bodies (synovial debris classically observed in patients with rheumatoid arthritis or tuberculosis), and chronic hemorrhage. Several well-written review articles about intra-articular masses are available in the radiology literature (21,22).
Other entities, such as pigmented villonodular synovitis and "primary" synovial (osteo)chondromatosis, also result in intra-articular masses that may require surgical debulking or biopsy. As patients with these disorders are treated at our institution by orthopedic oncologists, we considered their referral appropriate. However, patients with synovitis due to a rheumatologic condition or loose bodies in the joint secondary to prior trauma or osteoarthritis do not need to be referred to an orthopedic oncologist.
Recesses, Bursae, Cysts, and Ganglia
Distention of a synovial recess or bursa can produce a soft-tissue mass that may be misinterpreted as a neoplasm on MR examinations, particularly if it contains heterogeneous material (eg, loose bodies, nodular synovitis) or if the radiologist is not familiar with normal articular-bursal anatomy. A synovial recess is generally defined as a direct extension of a joint cavity, whereas a bursa is a synovium-lined compartment that exists separately from a joint (23). However, this distinction is not always clear, because what constitutes a bursa embryologically may appear at later imaging studies as a synovial recess, and vice versa. Articular communication with periarticular bursae is not uncommon (24). A list of commonly encountered recesses and bursae, compiled from various sources (2333), is provided in Table 4.
In our experience at the clinic, the knee has been the most common site of fluid- or debris-filled bursae. Fluid frequently is seen within the gastrocnemiosemimembranous bursa at MR imaging of the knee. Distention of this pouch results in a popliteal or Baker cyst. The diagnosis of a Baker cyst is easily made if one sees a fluid collection in the posteromedial compartment of the knee, with a "neck" that extends into the joint between the distal tendon of the semimembranosus muscle and the proximal tendon of the medial head of the gastrocnemius muscle. However, loose bodies, blood products, or other material filling the bursa may produce a more heterogeneous appearance that may lead to an incorrect diagnosis of neoplasm (Fig 11). Radiography may help confirm the presence of calcified or ossified loose bodies and allow an accurate diagnosis.

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Figure 11a. Popliteal cyst with ossified loose bodies in a 64-year-old woman. (a) Sagittal T2-weighted MR image of the knee shows an apparent mass with small internal foci of low signal intensity (arrowhead) posterior to the medial femoral condyle. (b) Axial intermediate-weighted fat-suppressed MR image shows round foci of low signal intensity (arrowhead) in the popliteal cyst. The "neck" of the cyst extends between the tendons of the semi-membranosus muscle (small arrow) and the medial head of the gastrocnemius muscle (large arrow). (c) Lateral radiograph shows ossified loose bodies (arrow) that correspond to the round low-signal-intensity foci seen on MR images. This case emphasizes the importance of knowing the bursal anatomy and correlating MR images with radiographs.
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Figure 11b. Popliteal cyst with ossified loose bodies in a 64-year-old woman. (a) Sagittal T2-weighted MR image of the knee shows an apparent mass with small internal foci of low signal intensity (arrowhead) posterior to the medial femoral condyle. (b) Axial intermediate-weighted fat-suppressed MR image shows round foci of low signal intensity (arrowhead) in the popliteal cyst. The "neck" of the cyst extends between the tendons of the semi-membranosus muscle (small arrow) and the medial head of the gastrocnemius muscle (large arrow). (c) Lateral radiograph shows ossified loose bodies (arrow) that correspond to the round low-signal-intensity foci seen on MR images. This case emphasizes the importance of knowing the bursal anatomy and correlating MR images with radiographs.
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Figure 11c. Popliteal cyst with ossified loose bodies in a 64-year-old woman. (a) Sagittal T2-weighted MR image of the knee shows an apparent mass with small internal foci of low signal intensity (arrowhead) posterior to the medial femoral condyle. (b) Axial intermediate-weighted fat-suppressed MR image shows round foci of low signal intensity (arrowhead) in the popliteal cyst. The "neck" of the cyst extends between the tendons of the semi-membranosus muscle (small arrow) and the medial head of the gastrocnemius muscle (large arrow). (c) Lateral radiograph shows ossified loose bodies (arrow) that correspond to the round low-signal-intensity foci seen on MR images. This case emphasizes the importance of knowing the bursal anatomy and correlating MR images with radiographs.
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Distended recesses and bursae typically have a signal intensity that is characteristic of fluid at MR imaging, and they enhance peripherally on images obtained after the intravenous administration of gadolinium. The diagnosis of less commonly distended recesses and bursae requires knowledge of their existence and their anatomic extent (Table 4). Several bursae around the knee may become inflamed and filled with fluid, conditions that may mimic a neoplasm at MR imaging (31). The cases we observed in the clinic involved the prepatellar bursa, the superficial infrapatellar bursa, and the pes anserine bursa. Cases involving recesses and bursae around the hip joint also are relatively common. Most radiologists are familiar with cases involving the trochanteric bursa; however, some patients referred to our clinic had MR images showing only distention of the iliopsoas and obturator externus bursae, both of which may communicate with the hip joint (2830). Patients with distended upper-extremity bursae were less frequently seen in the clinic. Distention of the subdeltoid bursa of the shoulder is common and usually can be diagnosed with confidence on the basis of anatomic location. Distention of the bicipitoradial bursa, however, is less commonly encountered and may mimic a tumor of the anterior elbow (26). The diagnosis of bursitis, like that of stress fractures, is reinforced by the clinical manifestation of pain, because most soft-tissue sarcomas are not painful.
Cysts and ganglia are fluid- or mucin-filled masses that typically occur around joints. They may cause symptoms and may require orthopedic surgical intervention; however, referral to an orthopedic oncologist is usually unnecessary. The distinction between what represents a cyst and what represents a ganglion is not clear, in large part because the pathogenesis of cysts and ganglia is uncertain (24,34). The terms often are used interchangeably.
Cysts and ganglia typically have homogeneous signal intensity similar to that of fluid (Fig 12a), although lobulation and septation frequently are evident. On MR images obtained after intravenous gadolinium is administered, a thin rim of peripheral enhancement is commonly seen, a feature that is occasionally accompanied by enhanced septal lines (Fig 12b). Paralabral cysts of the shoulder and acetabulum and parameniscal cysts of the knee are typically associated with underlying labral tears and meniscal tears, respectively (24,31). Identification of the underlying tear is essential for the diagnosis of a paralabral or parameniscal cyst, although the tear may not always be evident. In the knee, cysts and ganglia adjacent to the cruciate ligaments and the tibio-fibular joint are fairly common. In the shoulder, cysts arising above the acromioclavicular joint often represent an extension of fluid from the glenohumeral joint through a torn rotator cuff and acromioclavicular joint capsule (35). Cysts also may arise within muscle, and these, too, show signal intensity similar to that of fluid. Cysts in the rotator cuff musculature have been shown to be associated with underlying cuff tears (36). Ganglia are commonly found in the hands and feet, often adjacent to tendons. Cysts and ganglia may extend into adjacent bone; occasionally, these are seen as lucent lesions on radiographs.
The keys to diagnosing benign cysts and ganglia are knowing their common locations and recognizing the characteristic homogeneous fluidlike signal intensity and enhanced thin peripheral rim (and occasionally enhanced septa).

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Figure 12a. Ganglion of the Guyon canal in a 38-year-old man. (a) Axial T2-weighted MR image of the wrist shows a lobulated homogeneous mass (arrowhead) with fluid signal intensity volar to the hook of the hamate. (b) Axial T1-weighted fat-suppressed image of the wrist after intravenous administration of a gadolinium chelate shows only peripheral enhancement of the mass (arrowhead), a feature typical of a ganglion. Nearly 2% of patients referred to the Orthopaedic Oncology Clinic arrived with MR images that showed characteristic features of a juxta-articular cyst or ganglion that was misinterpreted as a potential malignancy. The signal intensity and enhancement patterns usually allow a confident diagnosis.
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Figure 12b. Ganglion of the Guyon canal in a 38-year-old man. (a) Axial T2-weighted MR image of the wrist shows a lobulated homogeneous mass (arrowhead) with fluid signal intensity volar to the hook of the hamate. (b) Axial T1-weighted fat-suppressed image of the wrist after intravenous administration of a gadolinium chelate shows only peripheral enhancement of the mass (arrowhead), a feature typical of a ganglion. Nearly 2% of patients referred to the Orthopaedic Oncology Clinic arrived with MR images that showed characteristic features of a juxta-articular cyst or ganglion that was misinterpreted as a potential malignancy. The signal intensity and enhancement patterns usually allow a confident diagnosis.
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Certain malignancies can be confused with benign cysts on unenhanced MR images. Synovial sarcoma is a malignant soft-tissue tumor that typically occurs near joints (particularly the knee) and can have a predominantly cystic appearance on MR images (Fig 13a). It occasionally mimics a synovial recess, bursa, or cyst; however, heterogeneously enhancing solid components are usually evident on contrast materialenhanced images (Fig 13b), and such findings should arouse suspicion about the presence of a neoplasm (21). Rarely, synovial sarcoma arises within a joint or bursa. Myxoid tumors (for example, myxoid liposarcoma) also appear cystic on unenhanced MR images but show more marked contrast enhancement than do synovial recesses, bursae, and cysts. The referral of a patient who is believed to have such a malignancy to an orthopedic oncologist is appropriate.

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Figure 13a. Synovial sarcoma in an 18-year-old man. (a) Axial T2-weighted fat-suppressed MR image of the knee shows a relatively homogeneously hyperintense mass (arrowhead) deep to the medial retinaculum. The mass mimics a large cyst. (b) Axial T1-weighted fat-suppressed MR image of the knee, obtained after the intravenous administration of a gadolinium chelate, shows diffuse enhancement of the mass (arrowhead), a finding indicative of a solid tumor. This patient was appropriately referred to the Orthopaedic Oncology Clinic.
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Figure 13b. Synovial sarcoma in an 18-year-old man. (a) Axial T2-weighted fat-suppressed MR image of the knee shows a relatively homogeneously hyperintense mass (arrowhead) deep to the medial retinaculum. The mass mimics a large cyst. (b) Axial T1-weighted fat-suppressed MR image of the knee, obtained after the intravenous administration of a gadolinium chelate, shows diffuse enhancement of the mass (arrowhead), a finding indicative of a solid tumor. This patient was appropriately referred to the Orthopaedic Oncology Clinic.
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Soft-Tissue Pitfalls
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Soft-Tissue Trauma
Musculotendinous injuries include myotendinous strain, muscle contusion, and tendon avulsion (37,38). A first-degree (mild) myotendinous strain results in edema without architectural distortion and hence is rarely confused with a neoplasm. Second- and third-degree strains are often accompanied by hematoma formation, and, in our experience, are more likely to be misinterpreted as neoplasms and to result in patient referral to our clinic (Fig 14). A contusion is caused by a direct blow to the muscle. MR imaging in such cases may show enlargement of and edema within the affected muscle. The edema may result in a feathery pattern like that seen in a first-degree myotendinous strain. However, a discrete mass is not evident unless a hematoma has formed. Complete tendon avulsion from the site of origin or insertion may mimic a soft-tissue neoplasm on cross-sectional images if the retracted tendon and muscle form a mass (Fig 15). The true nature of such a mass may be discovered through a careful evaluation of images in all planes to locate the torn end of the retracted tendon. A fragment of bone may come away with the avulsed tendon, and subsequent healing of the avulsion fracture may result in a prominent bone formation that mimics an aggressive neoplasm such as osteosarcoma on radiographs (Fig 16). This occurs most often in children and adolescents because of incompletely fused apophyses (39,40). The MR imaging appearance of such an injury may result in further confusion, particularly if the reactive bone formation produces a soft-tissue "mass" or if there is edema in the underlying bone. CT often helps secure the diagnosis by revealing the benign nature of ossification and depicting the donor site of the fracture. Like the healing process in an avulsion fracture, posttraumatic heterotopic ossification (myositis ossificans) may produce radiographic features that mimic a mineralized neoplasm (Fig 17). The MR imaging appearance is variable and depends on the maturity of the lesion (41).
Chronic ossification typically has an appearance comparable with that of bone, with peripheral low signal intensity and central high signal intensity on T1-weighted images. Earlier phases of myositis ossificans may mimic a soft-tissue neoplasm with heterogeneous low signal intensity on T1-weighted images, high signal intensity on T2-weighted images, and enhancement after gadolinium administration. Observation of a low-signal-intensity rim, which corresponds to early peripheral ossification, is suggestive of the diagnosis; however, this feature may be difficult to distinguish from a pseudocapsule surrounding a tumor. CT is usually the best imaging modality for characterizing the mass, which, unlike most soft-tissue malignancies, often demonstrates the most mature mineralization at its periphery (Fig 17). If the mineralization is nonspecific but myositis ossificans is suspected on the basis of the clinical history, then follow-up CT in 4 weeks may be necessary (38). Parosteal osteosarcomas may mimic myositis ossificans. These low-grade osteosarcomas arise on the surface of a bone (most commonly the femur) and ossify. Ossification of the tumor initially occurs at its base, adjacent to the underlying bone, and the ossified area is surrounded by a soft-tissue mass, whereas ossification in myositis ossificans first occurs peripherally.

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Figure 14a. Muscle strain injury in a 20-year-old man. (a) Axial T2-weighted MR image of the thigh shows a mass with high signal intensity (arrowhead) within the rectus femoris. (b) Axial T1-weighted MR image shows the location of the high-signal-intensity mass (arrowhead) adjacent to the distal tendon (arrow) of the rectus femoris muscle, findings compatible with a subacute hematoma from a previous myotendinous strain injury. The low-signal-intensity rim that partially surrounds the hematoma represents hemosiderin deposition. Knowledge of the MR imaging appearance of hematomas should allow the avoidance of a mistaken diagnosis of malignancy in most cases.
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Figure 14b. Muscle strain injury in a 20-year-old man. (a) Axial T2-weighted MR image of the thigh shows a mass with high signal intensity (arrowhead) within the rectus femoris. (b) Axial T1-weighted MR image shows the location of the high-signal-intensity mass (arrowhead) adjacent to the distal tendon (arrow) of the rectus femoris muscle, findings compatible with a subacute hematoma from a previous myotendinous strain injury. The low-signal-intensity rim that partially surrounds the hematoma represents hemosiderin deposition. Knowledge of the MR imaging appearance of hematomas should allow the avoidance of a mistaken diagnosis of malignancy in most cases.
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Figure 15a. Avulsion injury and tendon retraction in a 58-year-old woman. (a) Axial T2-weighted MR image of the proximal thigh shows an apparent mass with a rim of high signal intensity (arrowhead) in the posterior soft tissues. Note the absence of the normal hamstring musculature. (b) Coronal T2-weighted fat-suppressed MR image shows the retracted hamstring musculature surrounded by fluid (arrowhead).
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Figure 15b. Avulsion injury and tendon retraction in a 58-year-old woman. (a) Axial T2-weighted MR image of the proximal thigh shows an apparent mass with a rim of high signal intensity (arrowhead) in the posterior soft tissues. Note the absence of the normal hamstring musculature. (b) Coronal T2-weighted fat-suppressed MR image shows the retracted hamstring musculature surrounded by fluid (arrowhead).
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Figure 16a. Avulsion injury in a 15-year-old boy. (a) Anteroposterior radiograph of the right hip shows lobulated ossification (arrow) along the proximal ischium. (b) Coronal T2-weighted MR image of the pelvis shows high-signal-intensity edema within the right ischium (arrowhead) as well as at the origin of the hamstring musculature (arrow). (c) Transverse CT image through the pelvis shows an avulsion fracture (arrowhead) arising from the right ischium at the hamstring origin. Healing avulsion injuries in children may mimic an ossifying neoplasm on radiographs; MR imaging or CT may be useful for follow-up evaluation.
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Figure 16b. Avulsion injury in a 15-year-old boy. (a) Anteroposterior radiograph of the right hip shows lobulated ossification (arrow) along the proximal ischium. (b) Coronal T2-weighted MR image of the pelvis shows high-signal-intensity edema within the right ischium (arrowhead) as well as at the origin of the hamstring musculature (arrow). (c) Transverse CT image through the pelvis shows an avulsion fracture (arrowhead) arising from the right ischium at the hamstring origin. Healing avulsion injuries in children may mimic an ossifying neoplasm on radiographs; MR imaging or CT may be useful for follow-up evaluation.
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Figure 16c. Avulsion injury in a 15-year-old boy. (a) Anteroposterior radiograph of the right hip shows lobulated ossification (arrow) along the proximal ischium. (b) Coronal T2-weighted MR image of the pelvis shows high-signal-intensity edema within the right ischium (arrowhead) as well as at the origin of the hamstring musculature (arrow). (c) Transverse CT image through the pelvis shows an avulsion fracture (arrowhead) arising from the right ischium at the hamstring origin. Healing avulsion injuries in children may mimic an ossifying neoplasm on radiographs; MR imaging or CT may be useful for follow-up evaluation.
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Figure 17a. Posttraumatic heterotopic ossification in a 15-year-old boy. (a) Anteroposterior radiograph of the left hip shows soft-tissue ossification (arrows) overlying the superolateral acetabulum and proximal femur. (b) Axial T1-weighted MR image of the hip shows a mass (arrowhead) of heterogeneous signal intensity in the approximate location of the rectus femoris muscle. (c) Axial T2-weighted MR image reveals that the mass (arrowhead) is of heterogeneously high signal intensity. (d) Axial T1-weighted MR image obtained after the intravenous administration of a gadolinium chelate shows enhancement of the mass (arrowhead). (e) Axial CT image reveals peripheral ossification of the mass (arrowhead), a typical feature of myositis ossificans traumatica. Myositis ossificans may mimic a soft-tissue sarcoma on MR images, but CT often reveals the true nature of the mass.
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Figure 17b. Posttraumatic heterotopic ossification in a 15-year-old boy. (a) Anteroposterior radiograph of the left hip shows soft-tissue ossification (arrows) overlying the superolateral acetabulum and proximal femur. (b) Axial T1-weighted MR image of the hip shows a mass (arrowhead) of heterogeneous signal intensity in the approximate location of the rectus femoris muscle. (c) Axial T2-weighted MR image reveals that the mass (arrowhead) is of heterogeneously high signal intensity. (d) Axial T1-weighted MR image obtained after the intravenous administration of a gadolinium chelate shows enhancement of the mass (arrowhead). (e) Axial CT image reveals peripheral ossification of the mass (arrowhead), a typical feature of myositis ossificans traumatica. Myositis ossificans may mimic a soft-tissue sarcoma on MR images, but CT often reveals the true nature of the mass.
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Figure 17c. Posttraumatic heterotopic ossification in a 15-year-old boy. (a) Anteroposterior radiograph of the left hip shows soft-tissue ossification (arrows) overlying the superolateral acetabulum and proximal femur. (b) Axial T1-weighted MR image of the hip shows a mass (arrowhead) of heterogeneous signal intensity in the approximate location of the rectus femoris muscle. (c) Axial T2-weighted MR image reveals that the mass (arrowhead) is of heterogeneously high signal intensity. (d) Axial T1-weighted MR image obtained after the intravenous administration of a gadolinium chelate shows enhancement of the mass (arrowhead). (e) Axial CT image reveals peripheral ossification of the mass (arrowhead), a typical feature of myositis ossificans traumatica. Myositis ossificans may mimic a soft-tissue sarcoma on MR images, but CT often reveals the true nature of the mass.
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Figure 17d. Posttraumatic heterotopic ossification in a 15-year-old boy. (a) Anteroposterior radiograph of the left hip shows soft-tissue ossification (arrows) overlying the superolateral acetabulum and proximal femur. (b) Axial T1-weighted MR image of the hip shows a mass (arrowhead) of heterogeneous signal intensity in the approximate location of the rectus femoris muscle. (c) Axial T2-weighted MR image reveals that the mass (arrowhead) is of heterogeneously high signal intensity. (d) Axial T1-weighted MR image obtained after the intravenous administration of a gadolinium chelate shows enhancement of the mass (arrowhead). (e) Axial CT image reveals peripheral ossification of the mass (arrowhead), a typical feature of myositis ossificans traumatica. Myositis ossificans may mimic a soft-tissue sarcoma on MR images, but CT often reveals the true nature of the mass.
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Figure 17e. Posttraumatic heterotopic ossification in a 15-year-old boy. (a) Anteroposterior radiograph of the left hip shows soft-tissue ossification (arrows) overlying the superolateral acetabulum and proximal femur. (b) Axial T1-weighted MR image of the hip shows a mass (arrowhead) of heterogeneous signal intensity in the approximate location of the rectus femoris muscle. (c) Axial T2-weighted MR image reveals that the mass (arrowhead) is of heterogeneously high signal intensity. (d) Axial T1-weighted MR image obtained after the intravenous administration of a gadolinium chelate shows enhancement of the mass (arrowhead). (e) Axial CT image reveals peripheral ossification of the mass (arrowhead), a typical feature of myositis ossificans traumatica. Myositis ossificans may mimic a soft-tissue sarcoma on MR images, but CT often reveals the true nature of the mass.
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As mentioned earlier, hematomas in the extremities may manifest as soft-tissue masses that mimic neoplasms at MR imaging. However, the clinical history and the signal intensity pattern in the mass usually allow a confident diagnosis of hematoma (42). Increased signal intensity within a mass on unenhanced T1-weighted fat-suppressed images is suggestive of methemoglobin and a subacute hematoma (Fig 14b). A lack of enhancement after intravenous gadolinium administration also supports the diagnosis of hematoma, as do areas of relatively low signal intensity within or along the periphery of the mass on T2-weighted images, the latter being due to intracellular deoxyhemoglobin or hemosiderin deposition.
Malignant soft-tissue tumors may bleed, and it may be difficult to distinguish between a simple hematoma and a hemorrhagic neoplasm at MR imaging (38). Nodular or masslike enhancement following intravenous gadolinium administration is suggestive of a neoplasm, whereas a lack of enhancement essentially excludes that diagnosis. However, fibrovascular tissue within a hematoma may show some enhancement following gadolinium administration; furthermore, delayed imaging after gadolinium administration may allow diffusion of the contrast material into the hematoma, with resultant enhancement mimicking that in a tumor. If a hematoma is observed but an underlying soft-tissue neoplasm is suspected, then the hematoma should be followed up until it resolves, or biopsy should be considered.
Nontraumatic Muscle Edema and Inflammation
Edema in a muscle or a group of muscles may be seen at MR imaging in various nontraumatic and nonneoplastic conditions, including autoimmune myositis, subacute muscle denervation, recent surgery or radiation therapy, rhabdomyolysis, and compartment syndrome (38,43). Although myositis typically results in muscle edema and enlargement rather than a discrete tumoral mass, occasionally an infiltrative and aggressive masslike appearance may manifest at MR imaging and mimic a sarcoma (4345), particularly in cases of infectious myositis. What appears to be a mass in one imaging plane may be more confidently diagnosed as an inflamed muscle in another plane (Fig 18) if the muscle maintains its normal fusiform contour. Persistence of the normal feathery pattern of muscle signal intensity (despite signal alterations caused by edema) also argues against the presence of a tumor. More extensive inflammation results in the disappearance of this pattern, with enlargement of the affected muscle and edema of the fascial planes; stranding of the subcutaneous fat from cellulitis may be seen in cases of infectious myositis. An examination of the myotendinous junction may help distinguish inflammation from a neoplasm: Tendons typically are displaced by tumors but may retain their normal position within an inflamed muscle.

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Figure 18a. Inflammatory myopathy in a 39-year-old man. (a) Axial T1-weighted fat-suppressed MR image of the arm shows enhancement of the brachialis muscle (arrowhead), a finding that mimics a mass. (b) Sagittal T1-weighted fat-suppressed MR image shows diffuse enhancement of the distal brachialis muscle (arrowheads); the muscle maintains its normal contour, and no mass is evident, two features that oppose a diagnosis of neoplasm. Muscle injury may have a similar appearance on MR images.
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Figure 18b. Inflammatory myopathy in a 39-year-old man. (a) Axial T1-weighted fat-suppressed MR image of the arm shows enhancement of the brachialis muscle (arrowhead), a finding that mimics a mass. (b) Sagittal T1-weighted fat-suppressed MR image shows diffuse enhancement of the distal brachialis muscle (arrowheads); the muscle maintains its normal contour, and no mass is evident, two features that oppose a diagnosis of neoplasm. Muscle injury may have a similar appearance on MR images.
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An abscess also may mimic a tumor. The typical intramuscular abscess manifests as a thick rim of peripheral enhancement around a central non-enhancing region representative of pus. A diabetic muscle infarction may result in signal alterations and enhancement of muscle that might be mistaken for a tumor as well. The radiologist may suggest the diagnosis of infarction if he or she observes an irregular rim of enhancement within edematous musculature, without a focal mass or fluid collection, and if the clinical history includes poorly controlled diabetes and acute painful swelling of the affected extremity (46,47).
Necrotic or cystic tumors may mimic abscesses at MR imaging. Gadolinium administration in such cases often helps demonstrate nodular or masslike solid enhancing components in the tumor. It may be possible to distinguish neoplastic from nonneoplastic muscle abnormalities by using MR imaging, even without knowledge of the patients condition (eg, pain, fever, underlying disease processes). However, aspiration or tissue biopsy may be required in some instances, and referral to an orthopedic oncologist is certainly appropriate if there is a reasonable probability that the abnormality is a neoplasm (48).
Lipoma
Fat-containing soft-tissue masses of the extremities are one of the most common reasons for referral to the Orthopaedic Oncology Clinic. This is not surprising, as lipoma is the most common soft-tissue neoplasm (49). Although many of the patients who presented to our clinic with benign lipomas were referred for elective resection, a few were referred with reports that erroneously suggested a diagnosis of liposarcoma. A lipoma can be confidently diagnosed at MR imaging if all pulse sequences depict a mass with signal that is completely isointense to the signal of normal subcutaneous fat (Fig 19). The presence of a few nonenhancing thin (<2-mm) septa within the mass need not undermine confidence in a diagnosis of lipoma. In addition, the interdigitation of an intramuscular lipoma with skeletal muscle may create a striated appearance; this finding has not been described as occurring in liposarcomas, and it, too, allows a confident diagnosis of lipoma.

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Figure 19. Lipoma in a 49-year-old woman. Axial T1-weighted MR image shows a mass (arrowhead) in the musculature of the medial aspect of the right arm. The mass had homogeneous signal intensity characteristic of fat on all MR images, a finding indicative of a lipoma. Liposarcoma should not be included in the differential diagnosis.
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The so-called well-differentiated liposarcoma (Fig 20) is composed largely of fat but, unlike most lipomas, contains thick (>2-mm) septa, nodular or globular nonfatty elements, or a combination thereof (50). A small percentage of masses with an appearance typical of well-differentiated liposarcomas at MR imaging ultimately are diagnosed as lipomas with nonmalignant non-fatty elements at pathologic analysis; the initial misdiagnosis of such lesions probably is unavoidable. Although a well-differentiated liposarcoma has no metastatic potential, the referral of patients with such lesions to an orthopedic oncologist is appropriate, as the rate of local recurrence is high for deep-seated lesions. Furthermore, some well-differentiated liposarcomas over time undergo a change known as dedifferentiation, in which a dominant nonadipose nodule (usually a high-grade pleomorphic sarcoma or fibrosarcoma) larger than 1 cm arises within the mass. Dedifferentiation portends a poorer prognosis and requires a more aggressive approach to treatment (50).

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Figure 20. Well-differentiated liposarcoma in a 63-year-old woman. Axial T1-weighted MR image of the arm shows a predominantly fatty mass (arrowhead) with prominent septa. Focal areas with signal that is slightly hypointense to that of fat are indicative of nonadipose elements (*). Although such findings might be representative also of a benign lipoma with nonadipose elements, referral to an orthopedic oncologist is appropriate.
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Fatty elements also may be seen in soft-tissue hemangiomas and elastofibromas. The MR imaging appearance of these tumors has been well described in the literature (51,52), and further description in this article is unnecessary. Patients with such lesions may be referred to an orthopedic oncologist for elective resection.
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Summary
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A couple of observations can be made on the basis of our experience in the Orthopaedic Oncology Clinic. First, radiologists tend to overdiagnose nonfatty marrow on MR examinations as a potential neoplasm. Normal hematopoietic marrow and osteonecrosis have typical MR imaging features that should allow a confident diagnosis in most cases. The MR imaging appearances of Paget disease and fibroxanthoma (nonossifying fibroma) may not be familiar to radiologists and hence may lead to a diagnosis of malignancy; this underscores the importance of correlating MR images with radiographs, which show the usually pathognomonic appearance of these lesions. MR images of a suspected malignant lesion should never be interpreted without radiographic correlation. In addition, marrow edema may be due to trauma, osteonecrosis, or a host of other processes and should not invoke an automatic finding of neoplasm.
Second, radiologists tend to overdiagnose benign soft-tissue and juxta-articular conditions (eg, muscle edema, distended bursae, and cysts) as potential malignancies on MR images. MR imaging is generally the best modality for evaluating soft-tissue abnormalities; however, knowledge of the anatomy of joints and bursae and an appreciation of signal intensity and enhancement patterns that may be seen in nonneoplastic disease processes are essential for accurate diagnosis.
Our consideration of the entities described in this article was no doubt aided by the fact that when we reviewed the imaging studies, we were situated in the Orthopaedic Oncology Clinic, where we almost certainly had greater access to pertinent clinical data than did the radiologists at the referring institutions. Furthermore, other factors unrelated to the radiologists interpretation (eg, cosmetic deformity) may lead to referral to an orthopedic oncologist. Finally, very few of these entities undergo biopsy, and hence histologic confirmation of the consensus diagnoses made by the orthopedic oncology team is not usually available. Nevertheless, a radiologists report stating that a malignant neoplasm cannot be excluded but describing an entity with classically benign imaging features may leave the clinician with little choice but to refer the patient to a tumor specialist. The evaluation of solitary lesions in bone or soft tissue may be a daunting task, particularly for radiologists who do not see many bone and soft-tissue tumors. In many cases, the lesion clearly appears aggressive, and a confident diagnosis of malignancy can be rendered. In other cases, the lesion may be described as indeterminate despite evaluation with multiple modalities, and referral of the patient to an orthopedic oncologist is appropriate. The radiologist can be most useful by recognizing entities that are highly unlikely to represent malignancy and by confidently reporting them as benign, thereby sparing the patient an unnecessary trip to the tumor specialist.
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Footnotes
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See the commentary by Bancroft following this article.
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