DOI: 10.1148/rg.271065092
RadioGraphics 2007;27:189-205
© RSNA, 2007
Anatomically Based Guidelines for Core Needle Biopsy of Bone Tumors: Implications for Limb-sparing Surgery1
Patrick T. Liu, MD,
Scott D. Valadez, MD,
F. Spencer Chivers, MD,
Catherine C. Roberts, MD and
Christopher P. Beauchamp, MD
1 From the Departments of Radiology (P.T.L., S.D.V., F.S.C., C.C.R.) and Orthopedic Surgery (C.P.B.), Mayo Clinic College of Medicine, 13400 E Shea Blvd, Scottsdale, AZ 85259. Recipient of a Certificate of Merit award for an education exhibit at the 2005 RSNA Annual Meeting. Received May 5, 2006; revision requested August 14 and received September 18; accepted September 21. P.T.L. is a research consultant for the Bracco Group, and C.P.B. is a consultant for Zimmer; all remaining authors have no financial relationships to disclose.
Address correspondence to P.T.L. (e-mail: liu.patrick{at}mayo.edu).
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Abstract
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Diagnostic image-guided needle biopsy plays a vital role in the work-up and treatment of patients with extremity bone tumors. The radiologist and the orthopedic oncologic surgeon should take a team approach to this procedure, especially when the bone lesion might be a primary sarcoma for which limb-sparing surgery (LSS) would be considered. A set of anatomically based guidelines were developed that can be used by the radiologist, in combination with case-by-case consultation with the surgeon, to plan image-guided core needle biopsies of extremity long bone lesions that may be treatable with LSS. By using these guidelines, along with the aforementioned consultation, the radiologist will be able to preserve the patients chances of receiving optimal surgical treatment.
© RSNA, 2007
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Introduction
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Over the past 30 years, the prognosis for patients with primary bone malignancies of the extremities has greatly improved due to innovations in imaging, chemotherapy, and surgical techniques. Orthopedic oncologic surgeons can now remove bone sarcomas without amputation in the vast majority of patients, with only a limited loss of limb function, using a class of procedures known as limb-sparing surgery (LSS) (14). Radiologists often play an important role in the work-up of these patients by performing image-guided needle biopsy, which has been shown to be nearly as accurate as open biopsy for the diagnosis and staging of musculoskeletal sarcomas, but with fewer complications and lower costs (58).
Bone sarcomas have been shown to recur locally from tumor seeding along biopsy tracks after core needle biopsy (9,10), procedures that are generally performed with needles 16 gauge or larger (11). Survival rates for patients who experience local recurrence of these sarcomas are very low, even after repeat surgery (often amputation) and chemotherapy. Therefore, orthopedic oncologic surgical principles require that the biopsy track and immediately surrounding tissue be removed en bloc with the tumor at the time of resection (1215). The 5-year overall survival rates after local recurrence of osteogenic sarcoma or Ewing sarcoma are only 29% and 14%, respectively (16,17).
Although the recurrence risk has not been quantified for core needle biopsy tracks, it is perceived as a significant issue in the orthopedic oncologic surgery community (14,18). This perception is likely due to reports that the local recurrence rate for sarcomas after open biopsy procedures has been shown to increase over fivefold (from 7% to 38%) when the biopsy scar is not removed at the time of definitive tumor resection (9). Studies have shown that biopsy tracks from fine-needle aspiration (2225-gauge needles) do not pose a significant risk of tumor seeding (19); however, the accuracy of fine-needle aspiration biopsy is less than that of core needle biopsy in the evaluation of bone lesions (2022). Because core needle biopsy and fine-needle aspiration are complementary and are frequently performed together, we plan all needle biopsies of potential bone sarcomas as if the needle track will be resected en bloc with the tumor at the time of surgery.
In this article, we describe optimal planning of core needle biopsies of extremity long bone tumors and review the surgical implications of a poorly planned biopsy approach. In addition, we briefly discuss the "knowledge gap" that exists in the general radiology community regarding biopsy planning. We also discuss and illustrate some proposed biopsy guidelines that will help the radiologist ensure patients chances of receiving optimal surgical treatment.
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Biopsy Planning
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When planning a core needle biopsy of a bone lesion, the radiologist should first decide whether the lesion may possibly be a primary sarcoma. To avoid hurting the patients chances for successful surgery, nearly all bone lesions that are solitary should be included in this "possible sarcoma" category.
With the exception of a few benign bone lesions that may have characteristic imaging appearances (eg, fibrous dysplasia, osteochondroma, fibrous cortical defects), it is difficult to exclude sarcoma in solitary bone lesions on the basis of imaging findings alone. Necrotic or myxoid tumors, for instance, can mimic cysts, whereas tel-angiectatic osteosarcomas have been shown to mimic aneurysmal bone cysts at radiography, computed tomography (CT), and even magnetic resonance (MR) imaging (23).
On the other hand, a patient with a bone lesion that appears coincidentally with multiple widespread similar-appearing bone lesions need not be considered a candidate for LSS. In this situation, metastases would be strongly suspected, and surgical resection would almost certainly not be a treatment option. Core needle biopsy of the lesion would not need to be restricted to a planned incision and could be performed via the easiest, least complex pathway.
If the target bone lesion is considered to be a possible primary malignancy, the radiologist should consult with the orthopedic oncologic surgeon to select a biopsy entry site and pathway that would align with the plane of incision for potential surgery (24). This cooperative planning will ensure that the biopsy track could easily be removed with the tumor at the time of surgical resection, in case the lesion should prove to be a primary bone sarcoma treatable with LSS.
All available cross-sectional images should be reviewed during the planning process to ensure that the patient is eligible for LSS and to find the ideal site within the tumor for biopsy. It is important to visualize the interface between the tumor and nearby major neurovascular bundles, since contamination of major neurovascular structures can necessitate their surgical removal and disqualify the patient from future LSS (25). Invasion of an adjacent muscle will necessitate resection of a large portion of the muscle but not necessarily amputation. Joint involvement introduces increased complexity to the surgery by necessitating a total arthroplasty.
MR imaging is the imaging modality that best delineates tumor boundaries and interfaces with myofascial compartmental boundaries and neurovascular structures. CT better demonstrates permeative cortical bone destruction, bone erosion, and tumor matrix calcification. Osteolytic bone lesions should be examined to find regions of maximal cortical thinning or destruction for the easiest point of access; however, the biopsy track would still need to adhere to the plane of incision for planned LSS. Ultrasonography can be used to identify vascular areas in tumors that would be more likely than other areas to yield positive biopsy results, as well as any avascular areas that may be necrotic or cystic and therefore likely to yield only nondiagnostic tissue. Contrast materialenhanced MR images or CT scans can also be examined to find nonenhancing areas of tumors that could be necrotic or hemorrhagic and that should, therefore, be avoided during biopsy because of the likelihood of a nondiagnostic sample.
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Surgical Implications
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If a core needle bone biopsy were to pass through tissues outside the planned incision plane, the surgical procedure may have to be altered to include the potentially contaminated tissue in the resection. Less attractive alternatives for the patient would consist of either a wider irradiation field (if the tumor is radiosensitive) or a greater chance of local tumor recurrence at the biopsy site (Fig 1).

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Figure 1. Suboptimal biopsy of Ewing sarcoma in the distal right femur in a 36-year-old man. CT scan obtained during core needle biopsy performed at an outside institution without orthopedic oncologic surgical consultation reveals that the needle was incorrectly inserted using an anterior approach through the rectus femoris muscle. LSS was performed using the standard lateral approach, but the surgeon was forced to perform an additional resection of the anterior portion of the biopsy track. Postoperative knee extension was compromised. Despite the administration of preoperative radiation therapy and chemotherapy and clean surgical margins, the tumor recurred adjacent to the resected biopsy track 9 months later.
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LSS procedures were designed to allow removal and replacement of the tumor-containing bone while leaving intact the major neurovascular and myotendinous structures needed to maintain limb function. Patient outcome will suffer unnecessarily if additional, functionally important structures must be resected owing to a poorly planned biopsy approach.
A multicenter study conducted by the Musculoskeletal Tumor Society in 1996 (13) showed that inappropriately performed biopsies of musculoskeletal tumors posed a significant clinical problem. In a review of 597 cases, the authors found that 19% of patients with musculoskeletal tumors had encountered problems with initial image-guided and open biopsy that forced the orthopedic oncologic surgeon to perform more complex resection or order additional chemotherapy or radiation therapy (13).
Perhaps the most striking finding in this study was that poorly planned biopsies led to unnecessary amputations in 5%8% of patients (13). The authors concluded with a recommendation that biopsies of primary musculoskeletal sarcomas be performed only at institutions with active orthopedic oncologic surgery programs because of deficiencies in knowledge and training among the general radiology and surgery communities.
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Knowledge Gap
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Probably the major reason these deficiencies exist among the general radiology community is that the need to coordinate biopsy approaches with surgical plans is unique to musculoskeletal tumors and, therefore, not widely known among radiologists in other subspecialty areas. For organs outside the musculoskeletal system, surgeons do not routinely resect needle biopsy tracks when removing tumors. Even though tumor seeding along biopsy tracks has been reported and discussed in cases of tumors arising in the prostate gland, liver, kidney, lung, colon, pancreas, thyroid gland, and breast, the incidence of such tumor seeding is low (2633). Therefore, radiologists performing percutaneous biopsies of non-musculoskeletal tumors have been able to select biopsy pathways without concern for planned surgical incisions, instead considering only factors such as the shortest skin-to-lesion distance and the avoidance of neurovascular structures and adjacent organs.
Few articles have been published in the radiology or orthopedics literature detailing the correct methods for radiologists to plan biopsies of potential musculoskeletal sarcomas. The need for radiologists to discuss the biopsy approach with the orthopedic oncologic surgeon before performing biopsies of bone lesions has been briefly mentioned in two articles in the radiology literature dealing with bone biopsy techniques (34,35). The standard surgical approaches for LSS have been presented in several musculoskeletal tumor surgical textbooks (14,15,36); to our knowledge, however, only one article in the radiology literature and one in the orthopedics literature have described specific biopsy approaches based on these surgical guidelines (24,37), and these discussions were limited to biopsies of the proximal humerus, pelvis, distal femur, and proximal tibia.
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Proposed Biopsy Guidelines
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In Tables 14, we propose comprehensive planning guidelines for image-guided needle biopsies of potential sarcomas in the long bones of the extremities from the hips to the ankles (Tables 1, 2) and from the shoulders to the wrists (Tables 3, 4). Multiple levels in each extremity segment are discussed, since the relationships of the bones, compartmental anatomy, and neurovascular structures shift as one moves from proximal to distal. These biopsy guidelines are based on the standard surgical approaches used for LSS of the extremities (14,15,36). The recommended biopsy approaches are illustrated for various anatomic regions as follows: hip and upper leg, Figures 15; lower leg, Figures 68; upper arm, Figures 911; and elbow and forearm, Figures 12 and 13. Although MR imaging can usually delineate soft-tissue planes and neurovascular bundles better than CT, we have chosen to illustrate these approaches with CT scans, since CT is better suited for biopsy guidance. On the whole, CT is faster and more easily accessible than MR imaging and does not require any specialized biopsy equipment.

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Figure 2a. Coronal (a) and axial oblique (b) multi-planar reformatted CT images (inset in b shows the location of the section) show a normal left hip. An angled subtrochanteric approach (green strip) should be used for biopsy of lesions in the femoral neck or head. The greater trochanter bursa (outlined in red in a) and the hip joint capsule should be avoided. GM = gluteus maximus muscle, GMed = gluteus medius muscle, TFL = tensor fascia lata muscle, VL = vastus lateralis muscle.
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Figure 2b. Coronal (a) and axial oblique (b) multi-planar reformatted CT images (inset in b shows the location of the section) show a normal left hip. An angled subtrochanteric approach (green strip) should be used for biopsy of lesions in the femoral neck or head. The greater trochanter bursa (outlined in red in a) and the hip joint capsule should be avoided. GM = gluteus maximus muscle, GMed = gluteus medius muscle, TFL = tensor fascia lata muscle, VL = vastus lateralis muscle.
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Figure 3a. Three-dimensional volume-rendered (VR) CT images show a normal thigh. The green line on the lateral image (a) shows the standard lateral surgical incision site for LSS of lesions in the femur. The green line on the medial image (b) shows an additional surgical incision site for distal femoral medial lesions. Horizontal white lines indicate the levels at which the CT scans in Figure 4 were obtained.
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Figure 3b. Three-dimensional volume-rendered (VR) CT images show a normal thigh. The green line on the lateral image (a) shows the standard lateral surgical incision site for LSS of lesions in the femur. The green line on the medial image (b) shows an additional surgical incision site for distal femoral medial lesions. Horizontal white lines indicate the levels at which the CT scans in Figure 4 were obtained.
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Figure 4a. Contrast-enhanced CT scans of the left thigh obtained at the level of the proximal femoral diaphysis (a), midfemoral diaphysis (b), distal femoral diametaphysis (c), distal femoral metaphysis (d), and femoral condyles (e) demonstrate the recommended biopsy paths (green strips). BF-LH = long head of the biceps femoris muscle, BF-SH = short head of the biceps femoris muscle, GM = gluteus maximus muscle, VI = vastus intermedius muscle, VL = vastus lateralis muscle, VM = vastus medialis muscle.
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Figure 4b. Contrast-enhanced CT scans of the left thigh obtained at the level of the proximal femoral diaphysis (a), midfemoral diaphysis (b), distal femoral diametaphysis (c), distal femoral metaphysis (d), and femoral condyles (e) demonstrate the recommended biopsy paths (green strips). BF-LH = long head of the biceps femoris muscle, BF-SH = short head of the biceps femoris muscle, GM = gluteus maximus muscle, VI = vastus intermedius muscle, VL = vastus lateralis muscle, VM = vastus medialis muscle.
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Figure 4c. Contrast-enhanced CT scans of the left thigh obtained at the level of the proximal femoral diaphysis (a), midfemoral diaphysis (b), distal femoral diametaphysis (c), distal femoral metaphysis (d), and femoral condyles (e) demonstrate the recommended biopsy paths (green strips). BF-LH = long head of the biceps femoris muscle, BF-SH = short head of the biceps femoris muscle, GM = gluteus maximus muscle, VI = vastus intermedius muscle, VL = vastus lateralis muscle, VM = vastus medialis muscle.
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Figure 4d. Contrast-enhanced CT scans of the left thigh obtained at the level of the proximal femoral diaphysis (a), midfemoral diaphysis (b), distal femoral diametaphysis (c), distal femoral metaphysis (d), and femoral condyles (e) demonstrate the recommended biopsy paths (green strips). BF-LH = long head of the biceps femoris muscle, BF-SH = short head of the biceps femoris muscle, GM = gluteus maximus muscle, VI = vastus intermedius muscle, VL = vastus lateralis muscle, VM = vastus medialis muscle.
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Figure 4e. Contrast-enhanced CT scans of the left thigh obtained at the level of the proximal femoral diaphysis (a), midfemoral diaphysis (b), distal femoral diametaphysis (c), distal femoral metaphysis (d), and femoral condyles (e) demonstrate the recommended biopsy paths (green strips). BF-LH = long head of the biceps femoris muscle, BF-SH = short head of the biceps femoris muscle, GM = gluteus maximus muscle, VI = vastus intermedius muscle, VL = vastus lateralis muscle, VM = vastus medialis muscle.
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Figure 5a. Atypical bone infarct in the left femur at the level of the middiaphysis in a 64-year-old man. (a) CT scan obtained for prebiopsy planning with the patient in the left anterior oblique position shows the biopsy site facing upward. (b) CT fluoroscopic image obtained during biopsy shows the biopsy needle track immediately anterior to the lateral intermuscular septum.
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Figure 5b. Atypical bone infarct in the left femur at the level of the middiaphysis in a 64-year-old man. (a) CT scan obtained for prebiopsy planning with the patient in the left anterior oblique position shows the biopsy site facing upward. (b) CT fluoroscopic image obtained during biopsy shows the biopsy needle track immediately anterior to the lateral intermuscular septum.
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Figure 6a. Three-dimensional VR CT images show a normal lower leg. The green line on the anteromedial image (a) shows the standard surgical incision site for LSS of lesions in the tibia, whereas the green line on the lateral image (b) shows the standard surgical incision site for LSS of lesions in the fibula. Horizontal white lines indicate the levels at which the CT scans in Figure 7 were obtained.
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Figure 6b. Three-dimensional VR CT images show a normal lower leg. The green line on the anteromedial image (a) shows the standard surgical incision site for LSS of lesions in the tibia, whereas the green line on the lateral image (b) shows the standard surgical incision site for LSS of lesions in the fibula. Horizontal white lines indicate the levels at which the CT scans in Figure 7 were obtained.
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Figure 7a. Contrast-enhanced CT scans of the lower left leg obtained at the levels of the tibial plateau (a), proximal tibial metaphysis (b), middiaphysis (c), distal diaphysis (d), and distal metaphysis (e) demonstrate the recommended biopsy paths (green strips). EDL = extensor digitorum longus muscle, EHL = extensor hallucis longus muscle, FDL = flexor digitorum longus muscle, G-L = lateral head of the gastrocnemius muscle, PB = peroneus brevis muscle, PL = peroneus longus muscle, S = soleus muscle, TA = tibialis anterior muscle.
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Figure 7b. Contrast-enhanced CT scans of the lower left leg obtained at the levels of the tibial plateau (a), proximal tibial metaphysis (b), middiaphysis (c), distal diaphysis (d), and distal metaphysis (e) demonstrate the recommended biopsy paths (green strips). EDL = extensor digitorum longus muscle, EHL = extensor hallucis longus muscle, FDL = flexor digitorum longus muscle, G-L = lateral head of the gastrocnemius muscle, PB = peroneus brevis muscle, PL = peroneus longus muscle, S = soleus muscle, TA = tibialis anterior muscle.
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Figure 7c. Contrast-enhanced CT scans of the lower left leg obtained at the levels of the tibial plateau (a), proximal tibial metaphysis (b), middiaphysis (c), distal diaphysis (d), and distal metaphysis (e) demonstrate the recommended biopsy paths (green strips). EDL = extensor digitorum longus muscle, EHL = extensor hallucis longus muscle, FDL = flexor digitorum longus muscle, G-L = lateral head of the gastrocnemius muscle, PB = peroneus brevis muscle, PL = peroneus longus muscle, S = soleus muscle, TA = tibialis anterior muscle.
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Figure 7d. Contrast-enhanced CT scans of the lower left leg obtained at the levels of the tibial plateau (a), proximal tibial metaphysis (b), middiaphysis (c), distal diaphysis (d), and distal metaphysis (e) demonstrate the recommended biopsy paths (green strips). EDL = extensor digitorum longus muscle, EHL = extensor hallucis longus muscle, FDL = flexor digitorum longus muscle, G-L = lateral head of the gastrocnemius muscle, PB = peroneus brevis muscle, PL = peroneus longus muscle, S = soleus muscle, TA = tibialis anterior muscle.
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Figure 7e. Contrast-enhanced CT scans of the lower left leg obtained at the levels of the tibial plateau (a), proximal tibial metaphysis (b), middiaphysis (c), distal diaphysis (d), and distal metaphysis (e) demonstrate the recommended biopsy paths (green strips). EDL = extensor digitorum longus muscle, EHL = extensor hallucis longus muscle, FDL = flexor digitorum longus muscle, G-L = lateral head of the gastrocnemius muscle, PB = peroneus brevis muscle, PL = peroneus longus muscle, S = soleus muscle, TA = tibialis anterior muscle.
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Figure 8a. Osteomyelitis of the left tibia at the level of the proximal metaphysis in a 45-year-old woman. (a) CT scan obtained for prebiopsy planning shows the biopsy site facing upward. (b) CT fluoroscopic image obtained during core needle biopsy illustrates the recommended anteromedial approach.
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Figure 8b. Osteomyelitis of the left tibia at the level of the proximal metaphysis in a 45-year-old woman. (a) CT scan obtained for prebiopsy planning shows the biopsy site facing upward. (b) CT fluoroscopic image obtained during core needle biopsy illustrates the recommended anteromedial approach.
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Figure 9a. Three-dimensional VR CT images show a normal upper arm. The green line on the anterior image (a) shows the standard surgical incision site for LSS of lesions in the humerus. The green line on the medial image (b) shows the standard medial surgical incision site for LSS of lesions in the distal humerus. Horizontal white lines indicate the levels at which the CT scans in Figure 10 were obtained.
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Figure 9b. Three-dimensional VR CT images show a normal upper arm. The green line on the anterior image (a) shows the standard surgical incision site for LSS of lesions in the humerus. The green line on the medial image (b) shows the standard medial surgical incision site for LSS of lesions in the distal humerus. Horizontal white lines indicate the levels at which the CT scans in Figure 10 were obtained.
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Figure 10a. Contrast-enhanced CT scans of the left humerus obtained at the levels of the humeral neck (a), proximal diaphysis (b), middiaphysis (c), distal diaphysis (d), and humeral epicondyles (e) demonstrate the recommended biopsy paths (green strips). B = brachialis muscle, BB = biceps brachii muscle, B-L = long head of the biceps muscle, Br = brachioradialis muscle, B-S = short head of the biceps muscle, C = coracobrachialis muscle, D = deltoid muscle, D-A = anterior portion of the deltoid muscle, D-P = posterior portion of the deltoid muscle, Ssc = subscapularis muscle.
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Figure 10b. Contrast-enhanced CT scans of the left humerus obtained at the levels of the humeral neck (a), proximal diaphysis (b), middiaphysis (c), distal diaphysis (d), and humeral epicondyles (e) demonstrate the recommended biopsy paths (green strips). B = brachialis muscle, BB = biceps brachii muscle, B-L = long head of the biceps muscle, Br = brachioradialis muscle, B-S = short head of the biceps muscle, C = coracobrachialis muscle, D = deltoid muscle, D-A = anterior portion of the deltoid muscle, D-P = posterior portion of the deltoid muscle, Ssc = subscapularis muscle.
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Figure 10c. Contrast-enhanced CT scans of the left humerus obtained at the levels of the humeral neck (a), proximal diaphysis (b), middiaphysis (c), distal diaphysis (d), and humeral epicondyles (e) demonstrate the recommended biopsy paths (green strips). B = brachialis muscle, BB = biceps brachii muscle, B-L = long head of the biceps muscle, Br = brachioradialis muscle, B-S = short head of the biceps muscle, C = coracobrachialis muscle, D = deltoid muscle, D-A = anterior portion of the deltoid muscle, D-P = posterior portion of the deltoid muscle, Ssc = subscapularis muscle.
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Figure 10d. Contrast-enhanced CT scans of the left humerus obtained at the levels of the humeral neck (a), proximal diaphysis (b), middiaphysis (c), distal diaphysis (d), and humeral epicondyles (e) demonstrate the recommended biopsy paths (green strips). B = brachialis muscle, BB = biceps brachii muscle, B-L = long head of the biceps muscle, Br = brachioradialis muscle, B-S = short head of the biceps muscle, C = coracobrachialis muscle, D = deltoid muscle, D-A = anterior portion of the deltoid muscle, D-P = posterior portion of the deltoid muscle, Ssc = subscapularis muscle.
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Figure 10e. Contrast-enhanced CT scans of the left humerus obtained at the levels of the humeral neck (a), proximal diaphysis (b), middiaphysis (c), distal diaphysis (d), and humeral epicondyles (e) demonstrate the recommended biopsy paths (green strips). B = brachialis muscle, BB = biceps brachii muscle, B-L = long head of the biceps muscle, Br = brachioradialis muscle, B-S = short head of the biceps muscle, C = coracobrachialis muscle, D = deltoid muscle, D-A = anterior portion of the deltoid muscle, D-P = posterior portion of the deltoid muscle, Ssc = subscapularis muscle.
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Figure 11a. Chondromyxoid fibroma of the proximal left humerus in a 21-year-old man. (a) CT scan obtained for prebiopsy planning shows the biopsy site facing upward. (b) CT fluoroscopic image obtained during core needle biopsy shows the biopsy track just lateral to the cephalic vein and deltopectoral groove.
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Figure 11b. Chondromyxoid fibroma of the proximal left humerus in a 21-year-old man. (a) CT scan obtained for prebiopsy planning shows the biopsy site facing upward. (b) CT fluoroscopic image obtained during core needle biopsy shows the biopsy track just lateral to the cephalic vein and deltopectoral groove.
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Figure 12a. Three-dimensional VR CT images show a normal forearm. The green line on the dorsolateral image (a) shows the standard incision site for LSS of lesions in the radius. The green line on the dorsomedial image (b) shows the standard surgical incision site for LSS of lesions in the ulna. Horizontal white lines indicate the levels at which the CT scans in Figure 13 were obtained.
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Figure 12b. Three-dimensional VR CT images show a normal forearm. The green line on the dorsolateral image (a) shows the standard incision site for LSS of lesions in the radius. The green line on the dorsomedial image (b) shows the standard surgical incision site for LSS of lesions in the ulna. Horizontal white lines indicate the levels at which the CT scans in Figure 13 were obtained.
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Figure 13a. Contrast-enhanced CT scans of the forearm obtained at the level of the elbow (a), proximal forearm (b), middle forearm (c), distal forearm (d), and distal radioulnar joint (e) demonstrate the recommended biopsy paths (green strips) for LSS of lesions in the ulna and radius. A = anconeus muscle, APL = abductor pollicis longus muscle-tendon, Br = brachialis muscle-tendon, ECRB = extensor carpi radialis brevis muscle-tendon, ECRL = extensor carpi radialis longus muscle-tendon, ECU = extensor carpi ulnaris muscle-tendon, EI = extensor indicis muscle, EPB = extensor pollicis brevis muscle-tendon, FDP = flexor digitorum profundus muscle, R = radius, U = ulna.
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Figure 13b. Contrast-enhanced CT scans of the forearm obtained at the level of the elbow (a), proximal forearm (b), middle forearm (c), distal forearm (d), and distal radioulnar joint (e) demonstrate the recommended biopsy paths (green strips) for LSS of lesions in the ulna and radius. A = anconeus muscle, APL = abductor pollicis longus muscle-tendon, Br = brachialis muscle-tendon, ECRB = extensor carpi radialis brevis muscle-tendon, ECRL = extensor carpi radialis longus muscle-tendon, ECU = extensor carpi ulnaris muscle-tendon, EI = extensor indicis muscle, EPB = extensor pollicis brevis muscle-tendon, FDP = flexor digitorum profundus muscle, R = radius, U = ulna.
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Figure 13c. Contrast-enhanced CT scans of the forearm obtained at the level of the elbow (a), proximal forearm (b), middle forearm (c), distal forearm (d), and distal radioulnar joint (e) demonstrate the recommended biopsy paths (green strips) for LSS of lesions in the ulna and radius. A = anconeus muscle, APL = abductor pollicis longus muscle-tendon, Br = brachialis muscle-tendon, ECRB = extensor carpi radialis brevis muscle-tendon, ECRL = extensor carpi radialis longus muscle-tendon, ECU = extensor carpi ulnaris muscle-tendon, EI = extensor indicis muscle, EPB = extensor pollicis brevis muscle-tendon, FDP = flexor digitorum profundus muscle, R = radius, U = ulna.
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Figure 13d. Contrast-enhanced CT scans of the forearm obtained at the level of the elbow (a), proximal forearm (b), middle forearm (c), distal forearm (d), and distal radioulnar joint (e) demonstrate the recommended biopsy paths (green strips) for LSS of lesions in the ulna and radius. A = anconeus muscle, APL = abductor pollicis longus muscle-tendon, Br = brachialis muscle-tendon, ECRB = extensor carpi radialis brevis muscle-tendon, ECRL = extensor carpi radialis longus muscle-tendon, ECU = extensor carpi ulnaris muscle-tendon, EI = extensor indicis muscle, EPB = extensor pollicis brevis muscle-tendon, FDP = flexor digitorum profundus muscle, R = radius, U = ulna.
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View larger version (46K):
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Figure 13e. Contrast-enhanced CT scans of the forearm obtained at the level of the elbow (a), proximal forearm (b), middle forearm (c), distal forearm (d), and distal radioulnar joint (e) demonstrate the recommended biopsy paths (green strips) for LSS of lesions in the ulna and radius. A = anconeus muscle, APL = abductor pollicis longus muscle-tendon, Br = brachialis muscle-tendon, ECRB = extensor carpi radialis brevis muscle-tendon, ECRL = extensor carpi radialis longus muscle-tendon, ECU = extensor carpi ulnaris muscle-tendon, EI = extensor indicis muscle, EPB = extensor pollicis brevis muscle-tendon, FDP = flexor digitorum profundus muscle, R = radius, U = ulna.
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Biopsy techniques for primary soft-tissue sarcomas of the extremities have been described in two recent articles (37,38) and will not be discussed in detail here. The recommendations for image-guided biopsy of soft-tissue sarcomas are similar to those for biopsy of bone sarcomas, although the surgical approaches for soft-tissue sarcomas are targeted more specifically to the involved compartment. Biopsy tracks should still be located along the plane of the planned incision for the definitive resection surgery as noted by the orthopedic oncologic surgeon, thereby avoiding needle penetration and contamination of uninvolved myofascial compartments.
The guidelines presented in this article are not intended to be strictly applied to all bone tumor biopsy cases, since individual patients clinical situations and surgeons preferences will vary. For each case, we recommend that the radiologist review the relevant imaging studies with the surgeon whenever possible to determine the plane of the planned incision. Factors that may alter the usual surgical approach include (a) local tumor extension into the surrounding muscles, skin, or joint capsule; and (b) scarring and grafts from previous operations.
Because malignancies in the hands and feet call for surgical approaches to resection that will vary widely depending on tumor location, biopsy planning for masses in these regions is beyond the scope of this article. These biopsies should be performed only after the orthopedic surgeon has first been consulted regarding his or her planned approach for tumor resection.
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Biopsy Technique
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The choice of bone biopsy needle depends on the location of the lesion within the bone, the integrity of the overlying bone cortex, and the internal consistency of the target lesion. For lesions located more than a few centimeters beneath the skin, a coaxial system will allow multiple biopsy passes through a stationary sheath. Multiple sites within a lesion should be sampled to avoid nondiagnostic results that could arise from sampling a region of tumor necrosis or cystic degeneration.
If the lesion is intramedullary and covered by intact bone cortex, a biopsy needle system with a drill tip will provide the easiest and quickest access. Of the many bone biopsy needles that are commercially available, we have found the RADI Bonopty coaxial drill and biopsy needle system (RADI Medical Systems, Uppsala, Sweden), with a 14-gauge sheath and eccentrically cutting 15-gauge drill tip, to be the most effective in penetrating intact cortical bone (11).
Once the target lesion has been accessed, the internal consistency of the lesion will guide the choice of the core biopsy needle. For "hard" lesions that are sclerotic, calcified, ossified, or composed of intact trabeculae infiltrated with tumor cells, biopsy should be performed with a stiff bone-cutting needle at least 15 gauge in diameter. Fine-needle aspiration of hard lesions should be performed after core biopsy has been performed, with a needle 22 gauge or smaller. Without the access to the interior of a hard lesion afforded by a bone-cutting needle, the aspiration of material from the center of the lesion with a thin, flexible needle would be difficult.
In contrast, "soft" lesions that are composed of soft tissue or fluid usually yield little diagnostic tissue when sampled with bone-cutting needles. Adding vacuum suction by attaching a syringe to a bone-cutting needle, or substituting a soft-tissue biopsy needle combined with a vacuum syringe, will provide the highest biopsy yield for these soft lesions (39). Numerous soft-tissue biopsy needles are commercially available, and all of them typically yield satisfactory biopsy specimens.
Spring-loaded core biopsy needles are not well suited for bone biopsies. In hard lesions, the spring mechanism and needle are insufficiently strong for biopsy of intact or sclerotic bone. In soft lesions that are adjacent to or surrounded by intact bone, the use of these spring-loaded needles may be problematic owing to the possibility of damage to the fragile trochar.
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Conclusions
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By using the anatomically based guidelines presented in this article in combination with case-by-case consultation with the orthopedic oncologic surgeon, the radiologist should be able to plan a core needle biopsy of an indeterminate bone lesion in a manner that will ensure the patients chances of receiving optimal surgical treatment. If the biopsy results confirm the diagnosis of a primary bone sarcoma and LSS is elected, the surgeon will be able to resect the biopsy track using a standard incision, without the need for additional soft-tissue resection, radiation therapy, or amputation.
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Footnotes
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Abbreviations: LSS = limb-sparing surgery, VR = volume-rendered
See the commentary by Kransdorf following this article.
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References
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