Radiologic Evaluation of Tumors and Tumor-Like Lesions



Radiologic Evaluation of Tumors and Tumor-Like Lesions





Classification of Tumors and Tumor-like Lesions

Tumors, including tumor-like lesions, can generally be divided into two groups: benign and malignant. The latter group can be further subclassified into primary malignant tumors, secondary malignant tumors (from the transformation of benign conditions), and metastatic tumors (Fig. 16.1). All of these lesions can be still further classified according to their tissue of origin (Table 16.1). Table 16.2 lists benign conditions that have the potential for malignant transformation.

To understand the terminology applied to tumors and tumor-like lesions of the bone, it is important to redefine certain terms pertinent to lesions and their location in the bone. The term tumor generally means mass; in common radiologic and orthopedic parlance, however, it is the equivalent of the term neoplasm. By definition, a neoplasm, ruled by an uncontrolled process of aberrant cellular and morphologic mechanisms, demonstrates autonomous growth; if in addition it produces local or remote metastases, it is defined as a malignant neoplasm or malignant tumor. Beyond this (and not dealt with in this chapter) are specific histopathologic criteria for defining a tumor as benign or malignant. It is nevertheless worth mentioning that certain giant cell tumors, despite a “benign” histopathology, may produce distant metastases and that certain cartilage tumors, despite adhering to a benign histopathologic pattern, can behave locally like malignant neoplasms, even though this is detectable only radiologically. Moreover, certain lesions discussed here and termed tumor-like lesions are not true neoplasms but rather have a developmental or inflammatory origin. They are included in this chapter because they display an imaging pattern that is almost indistinguishable from that of true neoplasms. Their cause is, in some cases, still being debated.

Equally important is the redefinition of certain terms pertinent to the location of a lesion in the bone. In the growing skeleton, one can clearly distinguish the epiphysis, growth plate (physis), metaphysis, and diaphysis (Fig. 16.2A), and when lesions are located at these sites they are named accordingly. The greatest confusion is in the use of the term metaphysis. The metaphysis is a histologically very thin zone of active bone growth, adjacent to the growth plate. Consequently, for a lesion to be called metaphyseal in location, it must extend into and abut the growth plate. However, it is customary—however incorrect—to use the same term for locating a lesion after skeletal maturity has occurred. By the time of maturity, the growth plate is scarred, and neither the epiphysis nor metaphysis remains. More proper and less confusing would be a terminology such as articular end of the bone and shaft for locating lesions in the bone whose growth plate has been obliterated and whose metaphysis has ceased to exist (Fig. 16.2B). Some other terms used to describe the location of bone lesions are illustrated in Figure 16.3.


Radiologic Imaging Modalities

In general, the imaging of musculoskeletal neoplasms can be considered from three standpoints: detection, diagnosis (and differential diagnosis), and staging (Fig. 16.4). The detection of a bone or a soft-tissue tumor does not always require the expertise of a radiologist. The clinical history and the physical examination are often sufficient to raise the suspicion of a tumor, although radiologic imaging is the most common means of revealing one. The radiologic modalities most often used in analyzing tumors and tumor-like lesions include (a) conventional radiography, (b) angiography (usually arteriography), (c) computed tomography (CT), (d) magnetic resonance imaging (MRI); (e) scintigraphy (radionuclide bone scan), (f) positron emission tomography (PET) and PET-CT, and (g) fluoroscopy-guided or CT-guided percutaneous soft-tissue and bone biopsy.


Conventional Radiography

In most instances, the standard radiographic views specific for the anatomic site under investigation suffice to make a correct diagnosis (Fig. 16.5), which can subsequently be confirmed by biopsy and histopathologic examination. Conventional radiography yields the most useful information about the location and morphology of a lesion, particularly concerning the type of bone destruction, calcifications, ossifications, and periosteal reaction. Moreover, it is important to compare recent radiographic studies with earlier films. This point cannot be emphasized enough. The comparison can reveal not only the nature of a bone lesion (Fig. 16.6) but also its aggressiveness, a critical factor in a diagnostic workup. Chest radiography may also be required in cases of suspected metastasis, the most frequent complication of malignant lesions. This should be done before any treatment of a malignant primary bone tumor because most bone malignancies metastasize to the lung.







FIGURE 16.1 Classification of tumors and tumor-like lesions.








TABLE 16.1 Classification of Tumors and Tumor-like Lesions by Tissue of Origin
























































Tissue of Origin


Benign Lesion


Malignant Lesion


Bone forming (osteogenic)


Osteoma


Osteoid osteoma


Osteoblastoma


Osteosarcoma (and variants)


Juxtacortical osteosarcoma (and variants)


Cartilage forming (chondrogenic)


Enchondroma (chondroma)


Chondrosarcoma (central)



Periosteal (juxtacortical) chondroma


Enchondromatosis (Ollier disease)


Osteochondroma (osteocartilaginous exostosis, solitary or multiple)



Conventional


Mesenchymal


Clear cell


Dedifferentiated



Chondroblastoma


Chondrosarcoma (peripheral)



Chondromyxoid fibroma


Fibrocartilaginous mesenchymoma



Periosteal (juxtacortical)


Fibrous, osteofibrous, and fibrohistiocytic (fibrogenic)


Fibrous cortical defect (metaphyseal fibrous defect)


Nonossifying fibroma


Benign fibrous histiocytoma


Fibrous dysplasia (monostotic and polyostotic)


Fibrocartilaginous dysplasia


Focal fibrocartilaginous dysplasia of long bones


Periosteal desmoid


Desmoplastic fibroma


Osteofibrous dysplasia (Kempson-Campanacci lesion)


Ossifying fibroma (Sissons lesion)


Fibrosarcoma


Malignant fibrous histiocytoma


Vascular


Hemangioma


Glomus tumor


Cystic angiomatosis


Angiosarcoma


Hemangioendothelioma


Hemangiopericytoma


Hematopoietic, reticuloendothelial, and lymphatic


Giant cell tumor (osteoclastoma)


Langerhans cell histiocytosis


Lymphangioma


Malignant giant cell tumor


Histiocytic lymphoma


Hodgkin lymphoma


Leukemia


Myeloma (plasmacytoma)


Ewing sarcoma


Neural (neurogenic)


Neurofibroma


Neurilemoma


Morton neuroma


Malignant schwannoma


Neuroblastoma


Primitive neuroectodermal tumor (PNET)


Chordoma


Notochordal


Lipoma


Liposarcoma


Fat (lipogenic)


Simple bone cyst


Unknown


Aneurysmal bone cyst


Intraosseous ganglion


Adamantinoma










TABLE 16.2 Benign Conditions with Potential for Malignant Transformation



































Benign Lesion


Malignancy


Enchondroma (in the long or flat bonesa; in the short, tubular bones almost always as a part of Ollier disease or Maffucci syndrome)


Chondrosarcoma


Osteochondroma


Peripheral chondrosarcoma


Synovial chondromatosis


Chondrosarcoma


Fibrous dysplasia (usually polyostotic, or treated with radiation)


Fibrosarcoma


Malignant fibrous histiocytoma


Osteosarcoma


Osteofibrous dysplasiab (Kempson-Campanacci lesion)


Adamantinoma


Neurofibroma (in plexiform neurofibromatosis)


Malignant schwannoma


Liposarcoma


Malignant mesenchymoma


Medullary bone infarct


Fibrosarcoma


Malignant fibrous histiocytoma


Osteomyelitis with chronic draining sinus tract (usually more than 15-20 years duration)


Squamous cell carcinoma


Fibrosarcoma


Paget disease


Osteosarcoma


Chondrosarcoma


Fibrosarcoma


Malignant fibrous histiocytoma


a Some authorities believe that, at least in some “malignant transformations” of enchondroma to chondrosarcoma, there was in fact from the very beginning a malignant lesion masquerading as benign and not recognized as such.

b Some authorities believe that this is not a true malignant transformation but rather independent development of malignancy in the benign condition.



Computed Tomography

Although CT by itself is rarely helpful in making a specific diagnosis, it can provide a precise evaluation of the extent of a bone lesion and may demonstrate breakthrough of the cortex and involvement of surrounding soft tissues (Fig. 16.7). CT is moreover very helpful in delineating a bone tumor having a complex anatomic structure. The scapula (Fig. 16.8), pelvis (Fig. 16.9), and sacrum, for example, may be difficult to image fully with conventional radiographic techniques. At times, three-dimensional CT (3D CT) reconstructed images are used to better and more comprehensively demonstrate the tumors. This technique can be useful, for example, in depicting surface lesions of bone, such as osteochondroma (Fig. 16.10), parosteal osteosarcoma, or juxtacortical chondrosarcoma. CT examination is crucial in determining the extent and spread of a tumor in the bone if limb salvage is contemplated, so that a safe margin of resection can be planned (Fig. 16.11). It can effectively demonstrate the intraosseous extension of a tumor and its extraosseous involvement of soft tissues such as muscles and neurovascular bundles. CT is also useful for monitoring the results of treatment, evaluating for recurrence of a resected tumor, and demonstrating the effect of nonsurgical treatment such as radiation therapy or chemotherapy (Fig. 16.12). It is also helpful in evaluating soft-tissue tumors (Fig. 16.13), which on standard radiographs are indistinguishable from one another (with the exception of lipomas, which usually demonstrate low-density features), blending imperceptibly into the surrounding normal tissue.






FIGURE 16.2 Parts of the bone. (A) In the maturing skeleton, the epiphysis, growth plate, metaphysis, and diaphysis are clearly recognizable areas. (B) With skeletal maturity, distinct epiphyseal and metaphyseal zones have ceased to exist. The terminology for describing the location of lesions should alter accordingly. The inset illustrates an alternate terminology.






FIGURE 16.3 Terminology used to describe the location of lesions in the bone.

Contrast enhancement of CT images aids in the identification of major neurovascular structures and well-vascularized lesions. Evaluating the relationship between the tumor and the surrounding soft tissues
and neurovascular structures is particularly important for planning limb-salvage surgery.






FIGURE 16.4 Imaging of tumors. Imaging of musculoskeletal neoplasms can be considered from three aspects: detection, diagnosis and differential diagnosis, and staging. (Modified from Greenspan A, Jundt G, Remagen W. Differential diagnosis in orthopaedic oncology, 2nd ed. Philadelphia: Lippincott Williams & Wilkins; 2007.)


PET and PET-CT

Recently, 2-fluoro[fluorine-18]-2-deoxy-D-glucose (F-18 FDG) PET and PET-CT have emerged as very effective metabolic-anatomic imaging techniques for the assessment of variety of neoplastic conditions. The simultaneous detection and precise localization of metabolic and biochemical activities by PET combined with anatomic details obtained by CT into a single superimposed image provides the radiologist with an unique opportunity not only to make a distinction between the normal and pathologic processes but frequently between the various pathologic disorders as well. Although the most common use of PET-CT is to improve the staging of musculoskeletal tumors and evaluate their response to therapy and emergence of recurrences, this technique is also a powerful tool for the detection and evaluation of metastatic disease (Fig. 16.14; see also Figs. 2.29B and 2.32) and some primary musculoskeletal tumors (Fig. 16.15; see also Figs. 2.30 and 2.31). In addition, recent trials using dual-time point F-18 FDG PET to distinguish malignant tumors from benign conditions yielded promising results.






FIGURE 16.5 Specific location of a tumor. Anteroposterior (A) and lateral (B) radiographs of the right knee of a 13-year-old girl reveal a radiolucent lesion located eccentrically in the proximal epiphysis of the tibia, with sharply defined borders and a thin, sclerotic margin (arrows). Here, the lesion’s location and appearance on the standard radiographs led to the correct diagnosis of chondroblastoma.


Arteriography

Arteriography is used mainly to map out bone lesions and to assess the extent of disease. It is also used to demonstrate the vascular supply of a tumor and to locate vessels suitable for preoperative intraarterial chemotherapy as well as to demonstrate the area suitable for open biopsy because the most vascular area of a tumor contains the most aggressive component. Occasionally, arteriography can be used to demonstrate abnormal





tumor vessels, corroborating findings with conventional radiography (Fig. 16.16). Arteriography is often useful in planning for limb-salvage procedures because it demonstrates the regional vascular anatomy and thus permits a plan to be drawn up for the resection procedure. It is also sometimes used to outline the major vessels before resection of a benign tumor (Fig. 16.17), and it can be combined with an interventional procedure, such as embolization of hypervascular tumors, before further treatment (Fig. 16.18). In selected cases, arteriography may help make a differential diagnosis, such as of osteoid osteoma versus a bone abscess.






FIGURE 16.6 Comparison radiography: a simple bone cyst. (A) Anteroposterior radiograph of the left humerus in a 26-year-old woman with vague pain for 2 months shows an ill-defined lesion in the medullary region, with a periosteal reaction medially and laterally. There appear to be scattered calcifications in the proximal portion of the lesion. The possibility of a cartilage tumor such as chondrosarcoma was considered, but a radiograph taken 17 years earlier (B) shows an unquestionably benign lesion (a simple bone cyst) that had been treated by curettage and the application of bone chips. In view of this, the later findings were interpreted as representing a healed bone cyst. The patient’s pain was found to be related to muscle strain.






FIGURE 16.7 Soft-tissue extension of malignant tumor: effectiveness of CT. (A) Anteroposterior radiograph of the right proximal femur of a 70-year-old man shows a destructive lesion in the medullary portion of the bone (arrows) displaying focal chondroid calcifications. The soft-tissue extension of the tumor cannot be well evaluated. (B) Axial CT demonstrates a large soft-tissue mass, which on biopsy proved to be a chondrosarcoma.






FIGURE 16.8 CT of chondrosarcoma. Standard radiographs were ambiguous in this 70-year-old man with a palpable mass over the right scapula. However, two CT sections demonstrate a destructive lesion of the glenoid portion and body of the scapula (arrows) (A), with a large soft-tissue mass extending to the rib cage and containing calcifications (curved arrows) (B).






FIGURE 16.9 CT of osteosarcoma. (A) Standard anteroposterior radiograph of the pelvis was not sufficient to delineate the full extent of the destructive lesion of the iliac bone in this 66-year-old woman. (B) CT scan, however, showed a pathologic fracture of the ilium (arrow) and the full extent of soft-tissue involvement. The high Hounsfield values of the multiple soft-tissue densities suggested bone formation. Enhancement of the CT images with contrast agent showed an increased vascularity of the lesion. Collectively, the CT findings suggested a diagnosis of osteosarcoma that, although unusual for a person of this age, was confirmed by open biopsy.






FIGURE 16.10 Osteochondroma: effectiveness of 3D CT. (A) Conventional CT section through the chest shows an osteochondroma at the site of the anteromedial portion of the right forth rib (arrow). It is difficult to determine if the lesion is sessile or pedunculated. (B) 3D CT reconstructed image in maximum intensity projection (MIP) delivers a much more informative image of osteochondroma and allows one to characterize the internal architecture of the lesion; note typical chondroid matrix of the tumor. (C) 3D CT reconstructed image in shaded surface display (SSD) renders better conspicuity of the lesion; the pedicle of osteochondroma (arrow) is now clearly demonstrated. (From Greenspan A, Jundt G, Remagen W. Differential diagnosis in orthopaedic oncology, 2nd ed. Philadelphia: Lippincott Williams & Wilkins; 2007.)






FIGURE 16.11 Osteosarcoma: effectiveness of CT. (A) Anteroposterior radiograph of the left proximal femur of a 12-year-old boy demonstrates an osteolytic lesion in the intertrochanteric region, with a poorly defined margin and amorphous densities in the center associated with a periosteal reaction medially—features suggesting osteosarcoma, which was confirmed on open biopsy. Because a limb-salvage procedure was contemplated, a CT scan was performed to determine the extent of marrow infiltration and the required level of bone resection. The most proximal section (B) shows obvious gross tumor involvement of the marrow cavity of the left femur (arrow). A more distal section (C) shows no gross marrow abnormality, but a positive Hounsfield value of 52 units indicates tumor involvement of the marrow, which was not shown on the standard radiographs. By comparison, the section of the right femur shows a normal Hounsfield value of -26 for bone marrow.






FIGURE 16.12 Osteosarcoma after chemotherapy: effectiveness of CT. Before surgery, this 14-year-old girl with an osteosarcoma of the left femur underwent a full course of chemotherapy. (A) CT section before the therapy was begun shows involvement of the bone and marrow cavity. Note the soft-tissue extension of the tumor, with heterogeneous, amorphous tumor bone formation. After combined treatment with doxorubicin hydrochloride, vincristine, methotrexate, and cisplatin, a repeat CT scan (B) shows calcifications and ossifications in the periphery of the lesion, which represents reactive rather than tumor bone and demonstrates the success of chemotherapy. Radical excision of the femur and a subsequent histopathologic examination showed almost complete eradication of malignant cells, confirming the CT findings.






FIGURE 16.13 CT of malignant fibrous histiocytoma (MFH) of the soft tissue. A 56-year-old woman presented with a soft-tissue mass on the posteromedial aspect of the right thigh. (A) Lateral \ radiograph of the femur demonstrates only a soft-tissue prominence posteriorly (arrows). (B) CT section shows an axial image of the mass, which is contained by a fibrotic capsule. The overlying skin is not infiltrated. Despite the benign appearance, the mass proved on biopsy to be an MFH.






FIGURE 16.14 PET and PET-CT of metastases. A 61-year-old woman was diagnosed with lung carcinoma. (A) A whole-body PET scan shows several hypermetabolic foci in the internal organs, lymph nodes, and osseous structures, representing metastatic disease. The fused PET-CT images demonstrate metastatic lesions in the right scapula (B), thoracic vertebral body (C), and right ilium (D).






FIGURE 16.15 PET and PET-CT of primary bone and primary soft-tissue tumors. (A,B) A hypermetabolic focus in the proximal left fibula in a 23-year-old man proved to be an Ewing sarcoma. (C,D) A hypermetabolic lesion in the vastus lateralis and medialis in the proximal left thigh in a 58-year-old woman was diagnosed on histopathologic examination as MFH of the soft tissues.






FIGURE 16.16 Arteriography of dedifferentiated chondrosarcoma. (A) Anteroposterior radiograph of the pelvis in a 79-year-old woman with an 8-month history of pain in the right buttock and weight loss demonstrates a poorly defined destructive lesion of the right iliac bone, with multiple small calcifications and a soft-tissue mass extending into the pelvic cavity. Note the effect of the mass on the urinary bladder filled with contrast (arrow). A chondrosarcoma was suspected, and a femoral arteriogram was performed as part of the diagnostic workup. (B) Subtraction study of an arteriogram demonstrates hypervascularity of the tumor. Note the abnormal tumor vessels, encasement and stretching of some vessels, and “pulling” of contrast medium into small “lakes”—all characteristic signs of a malignant lesion. Biopsy revealed a highly malignant, dedifferentiated chondrosarcoma. In this case, the vascular study corroborated the radiographic findings of a malignant bone tumor.






FIGURE 16.17 Arteriography of osteochondroma. A 12-year-old boy with osteochondroma of the distal femur (arrow) underwent arteriography to demonstrate the relationship of the distal superficial femoral artery to the lesion. This subtraction study shows no major vessels near the planned site of resection at the base of the lesion, important information for surgical planning.


Myelography

Myelography may be helpful in dealing with tumors that invade the vertebral column and thecal sac (Fig. 16.19), although recently this procedure has been almost completely replaced by MRI.







FIGURE 16.18 Vertebral arteriography and embolization of hemangioma. A 73-year-old woman presented with a collapsed T11 vertebra, which showed a corduroy-like pattern suggestive of hemangioma. Vertebral angiography was performed. (A) Arteriogram of the 11th right intercostal artery outlines a vascular paraspinal mass associated with hemangioma and indicating extension of the lesion into the soft tissues. (B) After embolization, the lesion shows a marked decrease in vascularity. Subsequently, the patient underwent decompression laminectomy and anterior fusion at T10-11 using a fibular strut graft.


Magnetic Resonance Imaging

MRI is indispensable in evaluating bone and soft-tissue tumors. Particularly with soft-tissue masses, MRI offers distinct advantages over CT. There is improved visualization of tissue planes surrounding the lesion, for example, and neurovascular involvement can be evaluated without the use of intravenous contrast.

In the evaluation of intraosseous and extraosseous extensions of a tumor, MRI is crucial because it can determine with high accuracy the presence or absence of soft-tissue invasion by a tumor (Fig. 16.20). MRI has often proved to be superior to CT in delineating the extraosseous and intramedullary extent of the tumor and its relationship to surrounding structures (Fig. 16.21). By showing sharper demarcation between normal and abnormal tissue than CT, MRI—particularly in evaluation of the extremities—reliably identifies the spatial boundaries of tumor masses (Fig. 16.22), the encasement and displacement of major neurovascular bundles, and the extent of joint involvement. Spin echo (SE) T1-weighted

images enhance tumor contrast with bone, bone marrow, and fatty tissue, whereas SE T2-weighted images enhance tumor contrast with muscle and accentuate peritumoral edema. Axial and coronal images have been used in determining the extent of soft-tissue invasion in relation to important vascular structures. However, in comparison with CT, MR images do not clearly demonstrate calcification in the tumor matrix; in fact, large amounts of calcification or ossification may be almost undetectable. Moreover, MRI has been shown to be less satisfactory than CT in the demonstration of cortical destruction. It is important to realize that both MRI and CT have advantages and disadvantages, and circumstances exist in which either can be the preferential or complementary study. But it is even more important that the surgeon tell the radiologist who is performing and interpreting the study what information is needed.






FIGURE 16.19 Myelography of aneurysmal bone cyst. Initial radiographic examination of the lumbar spine of this 14-year-old girl with an 18-month history of pain in the lower back and sciatica of the left leg did not disclose any abnormalities; myelography was performed because of suspected herniation of a lumbar disk, but it was inconclusive. A repeat study was requested when the symptoms became more severe after 3 months. (A) Posteroanterior radiograph of the lumbosacral spine shows destruction of the left pedicle of L4 (arrow) and the left part of the L5 body (open arrows). Note the residual contrast in the subarachnoid space. A repeat myelogram using a water-soluble contrast (metrizamide) shows, on the posteroanterior view (B), extradural compression of the thecal sac on the left side with displacement of the nerve roots (arrows). Biopsy confirmed the radiographic diagnosis of an aneurysmal bone cyst.






FIGURE 16.20 MRI of chondrosarcoma. (A) Conventional radiograph of the left femur in anteroposterior projection of a 67-year-old woman demonstrates a tumor in the distal shaft destroying the medullary portion of the bone and breaking through the cortex. The soft-tissue extension cannot be determined. (B) Axial T2-weighted MR image (SE; repitition time [TR] 2500/echo time [TE] 70 msec) demonstrates a tumor infiltrating bone marrow, destroying the posterolateral cortex, and breaking into the soft tissues with the formation of a large mass (arrows). Compare with a normal contralateral extremity.






FIGURE 16.21 MRI of parosteal osteosarcoma. (A) From this lateral radiograph of the distal femur of a 22-year-old woman with parosteal osteosarcoma, it is difficult to evaluate if the tumor (arrow) is on the surface of the bone or already infiltrated through the cortex. (B) Sagittal T1-weighted MRI (SE; TR 500/TE 20 msec) demonstrates invasion of the cancellous portion of the bone, as represented by an area of low signal intensity (arrows).






FIGURE 16.22 MRI of MFH and osteosarcoma. (A) Coronal T1-weighted MRI (SE; TR 500/TE 20 msec) demonstrates involvement of the medullary cavity of the right femur in this 16-year-old girl with MFH (the entire tumor is not imaged on this study). Note the excellent demonstration of the interface between normal bone displaying high signal intensity and a tumor displaying intermediate signal intensity. (B) Coronal T1-weighted MRI in another patient with osteosarcoma of the distal femur demonstrates the intramedullary extension of the tumor. Again, note demonstration of sharp interface between tumor and not-affected bone. (C) Sagittal T2-weighted MRI shows a small focal area of cortical breakthrough in the anterior cortex of the distal femur (arrow) and posterior periosteal elevation (arrowhead). (D) Anteroposterior radiograph of the knee of another patient sows a sclerotic lesion within the medullary cavity of the proximal tibia (arrow). Note the subtle widening of the medial aspect of the physis (arrowhead), suspicious for trans-physeal extension of the tumor. (E) Coronal T1-weighted MRI of the proximal tibia outlines the intramedullary extent of osteosarcoma (long arrow), the extraosseous mass (short arrows), and confirms the extension of the tumor across the physis into the epiphysis (arrowhead). (F) Sagittal T2-weighted MR image demonstrates the intramedullary (long arrow) and extraosseous (arrowhead) extension of the tumor. Note the typical Codman triangle in the inferior aspect of the lesion (short arrow), and the surrounding bone marrow and soft-tissue edema.

Several investigators have stressed the superior contrast enhancement of MR images using intravenous injection of gadopentetate dimeglumine (gadolinium diethylenetriamine-penta-acetic acid [Gd-DTPA]). Enhancement was found to give better delineation of the tumor’s richly vascularized parts and of the compressed tissue immediately surrounding the tumor. It was also found to assist in the differentiation of intraarticular tumor extension from joint effusion, and, as Erlemann pointed out, improved the differentiation of necrotic tissue from viable areas in various malignant tumors.

According to the recent investigations, MRI may have an additional application in evaluating both the tumor’s response to radiation and chemotherapy and any local recurrence. On gadolinium-enhanced T1-weighted images, signal intensity remains low in avascular, necrotic areas of tumor while it increases in viable tissue. Although static MRI was of little value for the assessment of response to the treatment, dynamic MRI using Gd-DTPA as a contrast enhancement, according to Erlemann, had the highest degree of accuracy (85.7%) and was superior to scintigraphy, particularly in patients who were receiving intraarterial chemotherapy. In general, drug-sensitive tumors display slower uptake of Gd-DTPA after preoperative chemotherapy than do nonresponsive lesions. As Vaupel contended, the rapid uptake of Gd-DTPA by malignant tissues may be due to increased vascularity and more rapid perfusion of the contrast material
through an expanded interstitial space. The latest observation by Dewhirst and associates suggests that MR spectroscopy may also be useful in the evaluation of patients undergoing chemotherapy.

It must be stressed, however, that most of the time MRI is not suitable for establishing the precise nature of a bone tumor. In particular, too much faith has been placed in MRI as a method of distinguishing benign lesions from malignant ones. An overlap between the classic characteristics of benign and malignant tumors is often observed. Moreover, some malignant bone tumors can appear misleadingly benign on MR images and, conversely, some benign lesions may exhibit a misleadingly malignant appearance. Attempts to formulate precise criteria for correlating MRI findings with histologic diagnosis have been largely unsuccessful. Tissue characterization on the basis of MRI signal intensities is still unreliable. Because of the wide spectrum of bone tumor composition and their differing histologic patterns, as well as in tumors of similar histologic diagnosis, signal intensities of histologically different tumors may overlap or there may be variability of signal intensity in histologically similar tumors.

Trials using combined hydrogen-1 MRI and P-31 MR spectroscopy also failed to distinguish most benign lesions from malignant tumors. Despite the use of various criteria, the application of MRI to tissue diagnosis has rarely brought satisfactory results. This is because, in general, the small number of protons in calcified structures renders MRI less effective in diagnosing bone lesions, and hence, valuable evidence concerning the production of the tumor matrix can be missed. Moreover, as several investigations have shown, MRI is an imaging modality of low specificity. T1 and T2 measurements are generally of limited value for histologic characterization of musculoskeletal tumors. There are, however, some exceptions to this general rule. Some bone tumors demonstrate morphologic characteristic that allows a specific diagnosis, such as the typical “popcorn” appearance of chondroid matrix (Fig. 16.23) or “fluid-fluid” levels characteristic of aneurysmal bone cyst (see Fig. 20.19) and telangiectatic osteosarcoma (Fig. 16.24). Quantitative determination of relaxation times has not proved to be clinically valuable in identifying various tumor types, although, as noted by Sundaram, it has proved to be an important technique in the staging of osteosarcoma and chondrosarcoma. T2-weighted images in particular are a crucial factor in delineating extraosseous tumor extension and peritumoral edema as well as in assessing the involvement of major neurovascular bundles. Necrotic areas change from a low-intensity signal in the T1-weighted image to a very bright, intense signal in the T2-weighted image and can be differentiated from viable, solid tumor tissue. Although MRI cannot predict the histology of bone tumors, as Sundaram pointed out, it is a useful tool for distinguishing round cell tumors and metastases from stress fractures or medullary infarcts in symptomatic patients with normal radiographs, and, it can occasionally differentiate benign from pathologic fracture.






FIGURE 16.23 MRI of chondroid matrix. Axial T2-weighted (A), sagittal T1-weighted (B), and coronal short time inversion recovery (STIR) (C) images demonstrate a typical popcorn pattern of chondroid matrix in the bone marrow space of the distal femur. Note also the slight endosteal scalloping on the axial image (arrow).


Skeletal Scintigraphy

The radionuclide bone scan is an indicator of mineral turnover, and because there is usually enhanced deposition of bone-seeking radiopharmaceuticals in areas of bone undergoing change and repair, a bone scan is useful in localizing tumors and tumor-like lesions in the skeleton, particularly in such conditions as fibrous dysplasia, Langerhans cell histiocytosis, or metastatic cancer, in which more than one lesion is encountered (Fig. 16.25). It also plays an important role in localizing small lesions such as osteoid osteomas, which may not always be seen on conventional radiographs (see Fig. 17.11B). Although in most instances, a radionuclide bone scan cannot distinguish benign lesions from malignant tumors, because increased blood flow with increased isotope deposition and increased osteoblastic activity takes place in benign and malignant conditions, it is still occasionally capable of making such differentiation in benign lesions that do not absorb the radioactive isotope (Fig. 16.26). The radionuclide bone scan is sometimes also useful for differentiating multiple myeloma, which usually shows no significant uptake of the tracer, from metastatic cancer, which usually does.

Aside from routine radionuclide scans performed using 99mTc-labeled phosphate compounds, occasionally, 67Ga is used for the detection and staging of bone and soft-tissue neoplasms. Gallium is handled by the body much like iron in that the protein transferrin carries it in the plasma, and it also competes for extravascular iron-binding proteins such as lactoferrin. The administered dose for adults ranges from 3 mCi (111 MBq) to 10 mCi (370 MBq) per study. The exact mechanism of tumor uptake of gallium remains unsettled, and its uptake varies with tumor type. In particular, Hodgkin lymphomas and histiocytic lymphomas are prone to significant gallium uptake.




Tumors and Tumor-like Lesions of the Bone