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Chondroblastoma of Bone*
Arun J. Ramappa, M.D.†; Francis Y. I. Lee, M.D.‡; Peter Tang, M.D.§; Jeffrey R. Carlson, M.D.#; Mark C. Gebhardt, M.D.†; Henry J. Mankin, M.D.†
View Disclosures and Other Information
Investigation performed at the Orthopaedic Oncology Service, Massachusetts General Hospital, and Children's Hospital, Harvard Medical School, Boston, Massachusetts
*No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article. No funds were received in support of this study.
†Orthopaedic Service, Gray 604, Massachusetts General Hospital, Boston, Massachusetts 02114. E-mail address for H. J. Mankin: hmankin@partners.org.
‡Department of Orthopaedics, Columbia University School of Medicine, 622 West 168th Street, New York, N.Y. 10032.
§Orthopaedic Service, University of Pittsburgh, Kaufmann Building, 3471 Fifth Avenue, Pittsburgh, Pennsylvania 15213.
#751 J. Clyde Morris Boulevard, Newport News, Virginia 23601.

The Journal of Bone & Joint Surgery.  2000; 82:1140-1140 
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Abstract

Background: Chondroblastoma of bone is a rare lesion, and few large series have been reported. The purpose of this paper is to report forty-seven cases treated by one group of surgeons and to identify factors associated with more aggressive tumor behavior.

Methods: Seventy-three patients with chondroblastoma of bone were treated between 1977 and 1998. We were able to obtain historical data, imaging studies, histological findings, and adequate personal or telephone follow-up to determine the outcome for forty-seven patients.

Results: The lesions were distributed widely in the skeleton, but most were in the epiphyses or apophyses of the long bones, especially the proximal part of the tibia (eleven tumors) and the proximal part of the humerus (ten tumors). The principal presenting symptoms were pain and limitation of movement. The treatment consisted of a variety of procedures, but the majority of the patients had intralesional curettage and packing with allograft or autograft bone chips or polymethylmethacrylate. Most of the patients had an excellent functional result, although in three osteoarthritis developed in the adjacent joint. Seven patients (15 percent) had a local recurrence; three of them had a second recurrence and one, a third recurrence. One patient died of widespread metastases, and another who had metastases to multiple sites was alive and disease-free after aggressive treatment of the metastatic lesions.

Conclusions: While the size of the lesion, the age and gender of the patient, the status of the growth plate, and an aneurysmal-bone-cyst component to the tumor had no significant effect on the recurrence rate, lesions around the hip (the proximal part of the femur, the greater trochanter, and the pelvis) accounted for the majority (five) of the seven recurrent tumors and one of the two metastatic lesions.

Figures in this Article
    In a monumental paper written in 1931, Codman originally described an "epiphyseal chondromatous giant cell tumor of the proximal humerus."3 Although the diagnosis was subsequently correctly changed to chondroblastoma of bone by Jaffe and Lichtenstein in 19429, a tumor located at that site in children is still known as Codman's tumor2 (Fig. 1). As noted by many authors, the tumor most frequently presents in adolescence and seems to arise from secondary centers of ossification2,5,6,8,9,12,17,19. Most authorities agree that the cell of origin arises from the epiphyseal plate or some remnant of it2,8,9,17. The lesion is rare, accounting for approximately 1 to 2 percent of all benign bone tumors2,5,17,19.
    Most patients with chondroblastoma present with pain, which is often quite severe, and limitation of movement of the adjacent joint2,3,5,8,17,18,19. Radiographic and special imaging studies demonstrate a destructive lesion of the epiphyseal site, often with some expansion of the bone and a sclerotic margin2,5,12,18,20. Within the cartilaginous mass that contains the tumor, there is often punctate calcification2,12,19,20. Histologically, the lesion is quite distinct from other cartilage-containing tumors; it shows well defined chondroblasts with benign-appearing nuclei, multinucleated giant cells, chondroid and sometimes hyaline foci, and a pattern of tiny calcific bodies that surround the cells and hence have been named "chicken-wire calcification" (Fig. 2)2,5,9,17.
    Treatment has been highly variable but currently usually consists of curettage and packing with bone graft2,5,18,19. A relatively high rate of recurrence (10 to 35 percent) has been reported in the past, and metastasis has been described but is extremely rare2,5,10,11,14-16. Risk factors for these two forms of aggressive behavior (recurrence and metastasis) have not been clearly defined.
    The purpose of this article is to describe a series of forty-seven cases of chondroblastoma, all diagnosed, treated, and followed by our group, and to further define which factor or factors should be considered as possible evidence of more aggressive behavior and therefore conceivably dictate improved plans for management.
     
    Anchor for JumpAnchor for Jump
    +Fig. 1:Radiograph showing a Codman tumor, a proximal humeral chondroblastoma, principally based in the epiphysis but extending into the metaphysis of a sixteen-year-old boy.
     
    Anchor for JumpAnchor for Jump
    +Fig. 2:Microphotograph showing the classic histological characteristics of a chondroblastoma. Note especially the chondroblasts and the wire-like calcification (hematoxylin and eosin, ¥ 45).
     
    Anchor for JumpAnchor for Jump
    +Fig. 3:Magnetic resonance image of a chondroblastoma of the proximal part of the tibia in a sixteen-year-old boy. Note the possible invasion of the subchondral bone plate and the sclerotic changes around the lesion.
     
    Anchor for JumpAnchor for Jump
    +Fig. 4:Computed tomography scan of a chondroblastoma of the proximal part of the humerus in a twelve-year-old girl.
     
    Anchor for JumpAnchor for Jump
    +Fig. 5-A:Figs. 5-A and 5-B: Radiographs showing chondroblastomas in atypical locations.
    Fig. 5-A: A large acetabular lesion in a nineteen-year-old man.
     
    Anchor for JumpAnchor for Jump
    +Fig. 5-B:A lesion in the calcaneus of a twenty-six-year-old man.
     
    Anchor for JumpAnchor for Jump
    +Fig. 6:Light microphotograph of a specimen from a chondroblastoma with an aneurysmal-bone-cyst component. Note the presence of giant cells and the chondroid component (hematoxylin and eosin, ¥ 65).
    We reviewed the charts, imaging studies, and histological studies of seventy-three patients with chondroblastoma who had been treated by the Orthopaedic Oncology Service at the Massachusetts General Hospital, Boston, Massachusetts, and Boston Children's Hospital between 1977 and 1998. Of this group, twenty-six patients either were followed for too short a period or had received a major part of their care at another institution. We were able to obtain historical data, imaging studies, histological findings, and adequate follow-up by means of a personal visit or telephone communication to determine the results of treatment for the remaining forty-seven patients, who constituted our series. We identified the age at presentation, gender, anatomical site, presenting symptoms, physical findings, and treatment methods. By reviewing the imaging studies, we were able to define the location within the bone (the epiphysis or the metaphysis, or both), the size of the tumor, the presence or absence of growth-plate closure, and the amount of cortical destruction. The histological findings were reviewed, and the presence or absence of an aneurysmal-bone-cyst component was particularly noted. Operative complications, whether there had been a recurrence, current status in relation to the tumor, and functional status were also determined for each of the patients in the study. Recurrence rates were analyzed in relation to all of the above parameters, and statistical analyses with use of chi-square methods and power studies were performed.
    The average age at presentation (and standard deviation) was 22 9.9 years (range, eleven to fifty-six years). Twenty-nine (62 percent) of the patients were between ten and twenty years of age. The average duration of follow-up was 88 35 months (range, twenty-six to 240 months).
    Eleven tumors were located in the proximal part of the tibia (Fig. 3); ten, in the proximal part of the humerus (Fig. 4); and four each, in the proximal part of the femur, the greater trochanter, the hemipelvis (Fig. 5-A), and the distal part of the femur. Two lesions each were located in the calcaneus (Fig. 5-B), the talus, and the scapula, and one each was located in the patella, the distal part of the radius, the distal part of the humerus, and the proximal part of the fibula.
    Twenty-nine of the thirty-two tumors in the long bones were in the epiphyseal or apophyseal part, even when the epiphysis was closed. Twelve of the epiphyseal tumors involved the metaphysis as well. Only one of the lesions in the long bones was metaphyseal.
    The physis remained open and presumably functional in twelve patients, who had ages ranging from eleven to fourteen years. Five tumors, all in the proximal part of the humerus or the proximal part of the tibia, had violated the growth plate.
    All forty-seven tumors had the typical histological appearance of a chondroblastoma, and the histological features of the seven recurrent tumors and the two that metastasized were indistinguishable from those of the other tumors. Five tumors had violated the articular cartilage. An aneurysmal-bone-cyst component was identified in eleven of the tumors4,19 (Fig. 6).
    It was possible to estimate the sizes of forty of the forty-seven tumors, which averaged 4.5 centimeters (range, one to eleven centimeters) in their longest diameter.
    The primary treatment for these lesions varied and included curettage and packing with allograft (seventeen tumors); curettage and packing with polymethylmethacrylate (eight); curettage and packing with iliac crest autograft (seven); curettage alone (five); marginal resection (four); resection and allograft replacement in the proximal part of the humerus (two), the distal part of the femur (one), and the glenoid (one); curettage and fat implantation (one); and marginal resection without packing (one). The seven recurrences were treated with intralesional resection (two), curettage and packing with iliac crest autograft (one), resection and allograft implantation (two), curettage and packing with allograft (one), and radiofrequency ablation (one).

    Complications of Surgery

    The complications of surgery were not insubstantial. One patient required another operative procedure after no diagnostic tissue was obtained initially. In another patient, the hip became painful after curettage and bone-grafting of a proximal femoral lesion and subsequently required an osteotomy. One patient sustained an undisplaced subtrochanteric fracture in a postoperative fall. Four of the six patients who had osteoarticular allograft as well as three others in whom hardware had been implanted required hardware removal several years after the surgery. One scapular lesion and both talar lesions ultimately resulted in osteoarthritis of the adjacent joint. One patient had a limb-length discrepancy and angular deformity of the affected limb postoperatively.

    Recurrence

    Forty of the forty-seven tumors did not recur. The average duration of follow-up for this group was 84 51.3 months (range, twenty-six to 196 months), and the average age was 21 9 years (range, eleven to forty-six years). Twenty-four of these patients were twenty years of age or younger, and sixteen were older. Twenty-five patients were male and fifteen were female. The average size of the lesion was 3.7 3.4 centimeters (range, one to ten centimeters). The growth plate was documented to be open in ten patients. Five tumors involved only the epiphysis, and five crossed the physis.
    Seven of the patients had a recurrence. The duration of follow-up averaged 106 72.4 months (range, thirty-two to 240 months). The average age for this group was 23 15.7 years (range, eleven to fifty-six years). Five of the seven patients were twenty years of age or younger. There were four male and three female patients, and the average size of the lesion was 5.3 4.6 centimeters (range, two to eleven centimeters). Two patients had open physes, and both tumors involved a secondary center of ossification. Three of the tumors were originally treated with curettage and allograft; two, with curettage and iliac crest autograft; one, with intralesional resection; and one, with curettage alone. Four of the tumors recurred a second time: two of these recurrences were treated with curettage and allograft, and one each was treated with intralesional resection and radiofrequency ablation. Only one of the four recurred a third time. The third recurrence was treated with curettage and osteoarticular allograft, and the tumor had not recurred again at five years.
    With the small numbers available, there was no significant difference between the nonrecurrent and the recurrent tumors with regard to the age or gender of the patient, size of the lesion, duration of follow-up, or method of primary or secondary treatment. Only one feature stood out: there were no recurrences in the eight patients treated with implantation of polymethylmethacrylate, whereas the tumor recurred in three of the seventeen patients in whom allograft had been implanted and in two of the seven in whom iliac crest autograft had been used. Although these data are suggestive, they were not significant on chi-square analysis because a power study indicated that the total sample size necessary to arrive at a 95 percent confidence level would be eleven patients treated with cement and thirty-four treated with graft.
    Another finding that could potentially influence the recurrence rate was the presence of an aneurysmal-bone-cyst component, which was noted histologically in eleven of the forty-seven tumors. Two of these eleven tumors recurred, compared with five of the thirty-six that did not have a cystic component. This small difference was not significant.
    The only significant difference between the nonrecurrent and the recurrent tumors was related to their locations. The most common sites of recurrence were the proximal part of the femur and the greater trochanter; four of eight tumors in those locations recurred. One of the four tumors in the pelvis also recurred, so a total of five of twelve lesions around the hip recurred. This recurrence rate differs markedly from that at all of the other sites, for which the rate was two (6 percent) of thirty-five. This difference was significant according to the Fisher exact test at the p < 0.03 level.

    Current Status of the Patients

    Metastases developed in two patients in our series. A twenty-nine-year-old man presented with a pelvic lesion in 1981, which was treated by intralesional resection. The tumor recurred locally three years later and was again treated by resection. A second recurrence two years later was treated by wide resection. In 1994, thirteen years after the primary tumor was discovered, the patient had had metastases to the sternum, multiple long-bone sites, and the lungs, and he died of the disease one year later. The metastatic lesions were identified histologically as chondroblastoma not unlike the primary tumor of the pelvis. The second patient was initially seen, at another center, at the age of forty-nine years with a chondroblastoma of a rib, and a resection was performed. A recurrence was noted one year later, and it was also resected. Six years later, at the age of fifty-six years, he presented to our institution with a chondroblastoma of the proximal part of the femur and he subsequently had an additional recurrence at that site as well as metastases to the scalp and neck and later to the pubis. All of the soft-tissue lesions were excised, and the pubic lesion was treated with radiofrequency ablation. At the time of writing, the patient was disease-free but was still being followed closely.
    At the time of the most recent follow-up, thirty-nine of the remaining forty-five patients stated that they were pain-free and had only minimal functional limitation. However, the two patients who had had a talar lesion had peritalar arthritis. Two of the patients with proximal femoral disease had a painful hip, and one of them had had an osteotomy for the treatment of malalignment that resulted from a pathological fracture through the lesion. One patient with a glenoid lesion had a painful glenohumeral joint with limited motion, and one patient with a pelvic lesion was receiving disability compensation because of pain of unknown cause.
    We are reporting on a large series of patients with chondroblastoma who were treated operatively by one group of surgeons. Most of our data coincide with the results of other studies1,5-8,12,13,17-20. For example, male patients were affected more frequently than female patients, and, except for three, all of our patients presented with pain. The two most frequent sites of involvement were the proximal part of the humerus and the proximal part of the tibia, as has been reported in other series5,17,19. All but one of the long-bone lesions in our patients arose from a secondary center of ossification. One lesion was primarily metaphyseal, a rare occurrence1,7,13. Four of the lesions arose in the talus or calcaneus7.
    Our patients were older than those in previous reports1,8,17,19. In our series, 62 percent of the forty-seven patients were twenty years of age or younger, whereas 82 percent of seventy patients were twenty years or younger in the study by Springfield et al.19 and 73 percent of 231 were twenty years or younger in the composite series reported by Huvos and Marcove8. The average age at the time of presentation in our series was twenty-two years, and, as might be expected, we had a lower percentage of patients with open growth plates compared with the rates in other reports. Furthermore, patients with a lesion that had not occurred in a long bone tended to be older than those with a long-bone lesion. It is unclear why our patient population was older, but the reason may be related to the referral pattern for our center.
    We attempted to identify risk factors for recurrence of chondroblastoma, the rate of which was lower in our series than in those reported by others2,5,8,17,19. The ages of the patients with and without recurrence were similar. Although the finding was not significant, the lesions that recurred were on the average larger than those that did not (5.3 compared with 3.7 centimeters). Open growth plates have been considered to be a risk factor for recurrence2,4,5,19. It has been hypothesized that tumors in patients with open growth plates are more likely to recur secondary to less aggressive surgical curettage due to fear of injury to the physis19. However, in our study, patients with open growth plates did not have a significantly increased rate of recurrence. It is believed that 20 percent of chondroblastomas have an aneurysmal cystic component, which has been described as a precursor to recurrence4,5. This was not observed in our series.
    The only factors that seemed to affect the recurrence rate were anatomical location and, to a lesser extent, the method of treatment. Five of twelve lesions in the proximal part of the femur, the greater trochanter, or the pelvis recurred, and one of the tumors in the pelvis and another that developed first in a rib and then in the pelvis metastasized. One possible explanation for this phenomenon is difficulty with gaining access to these lesions because of the proximal femoral and pelvic anatomy combined with the surgeon's concern about compromising the blood supply to the femoral head. However, this anatomical site is known for harboring more aggressive lesions, particularly cartilage tumors2,18, and that may be the reason for the higher recurrence rate.
    Although the finding was not significant, perhaps because of the small number of patients, the recurrence rate in our series varied among the different treatment methods. Intralesional curettage was associated with a higher recurrence rate (one of five) than was marginal resection (none of four). Curettage and packing with bone graft was associated with a higher recurrence rate (21 percent) than was curettage and packing with polymethylmethacrylate (0 percent). The heat of polymerization of the cement may destroy residual tumor after curettage. On the basis of this finding, we now recommend that polymethylmethacrylate be chosen over bone graft to fill defects after removal of worrisome or recurrent lesions.
    Two patients had metastases, and one died. One case involved the pelvis, a site known to harbor more aggressive lesions. The second case had some unusual characteristics, including older age at presentation (forty-nine years), involvement of a rib (known to be an uncommon site13), and the development of a metachronous lesion some years later.
    On the basis of this study, we concluded that although chondroblastomas have a substantial recurrence rate and their juxta-articular nature can lead to arthritic changes secondary to treatment, surgery that is more aggressive than curettage and packing with polymethylmethacrylate is not warranted for classic chondroblastomas and even local recurrences should be treated in a similar fashion.
    Brien, E. W.; Mirra, J. M.; and Ippolito, V.: Chondroblastoma arising from a nonepiphyseal site. Skel. Radiol.,24: 220-222, 1995.24220  1995 
     
    Campanacci, M.: Bone and Soft Tissue Tumors: Clinical Features, Imaging, Pathology and Treatment. Ed. 2, pp. 247-264. New York, Springer, 1999. 
     
    Codman, E. A.: Epiphyseal chondromatous giant cell tumors of the upper end of the humerus. Surg., Gynec. and Obstet.,52: 543-548, 1931.52543  1931 
     
    Crim, J. R.; Gold, R. H.; Mirra, J. M.; and Eckardt, J.: Case report 748: chondroblastoma of the femur with an aneurysmal bone cyst. Skel. Radiol.,21: 403-405, 1992.21403  1992 
     
    Dahlin, D. C., and Ivins, J. C.: Benign chondroblastoma. A study of 125 cases. Cancer,,30: 401-413, 1972.30401  1972 
     
    Fechner, R. E., and Wilde, H. D.: Chondroblastoma in the metaphysis of the femoral neck. J. Bone and Joint Surg.,56-A: 413-415, March 1974.56-A413  1974 
     
    Fink, B. R.; Temple, H. T.; Chiricosta, F. M.; Mizel, M. S.; and Murphey, M. D.: Chondroblastoma of the foot. Foot and Ankle Internat.,18: 236-242, 1997.18236  1997 
     
    Huvos, A. G., and Marcove, R. C.: Chondroblastoma of bone: a critical review. Clin. Orthop.,95: 300-312, 1973.95300  1973  [PubMed]
     
    Jaffe, H. L., and Lichtenstein, L.: Benign chondroblastoma of bone. A reinterpretation of the so-called calcifying or chondromatous giant cell tumor. Am. J. Pathol.,18: 969-991, 1942.18969  1942  [PubMed]
     
    Kahn, L. B.; Wood, F. M.; and Ackerman, L. V.: Malignant chondroblastoma. Report of two cases and review of the literature. Arch. Pathol.,,88: 371-376, 1969.88371  1969 
     
    Kyriakos, M.; Land, V. J.; Penning, H. L.; and Parker, S. G.: Metastatic chondroblastoma. Report of a fatal case with a review of the literature on atypical, aggressive, and malignant chondroblastoma. Cancer,55: 1770-1789, 1985.551770  1985  [PubMed]
     
    McLeod, R. A., and Beabout, J. W: The roentgenographic features of chondroblastoma. Am. J. Roentgenol.,118: 464-471, 1973.118464  1973 
     
    Mayo-Smith, W.; Rosenberg, A. E.; Khurana, J. S.; Kattapuram, S. V.; and Romero, L. H.: Chondroblastoma of the ribs. A case report and review of the literature. Clin. Orthop.,251: 230-234, 1990.251230  1990  [PubMed]
     
    Mirra, J. M.; Ulich, T. R.; Eckardt, J. J.; and Bhuta, S.: "Aggressive" chondroblastoma. Light and ultramicroscopic findings after en bloc resection. Clin. Orthop.,178: 276-284, 1983.178276  1983  [PubMed]
     
    Riddell, R. J.; Louis, C. J.; and Bromberger, N. A.: Pulmonary metastases from chondroblastoma of the tibia: report of a case. J. Bone and Joint Surg.,55-B(4): 848-853, 1973.55-B(4)848  1973 
     
    Rodgers, W. B., and Mankin, H. J.: Metastatic malignant chondroblastoma. Am. J. Orthop.,25: 846-849, 1996.25846  1996  [PubMed]
     
    Schajowicz, F., and Gallardo, H.: Epiphysial chondroblastoma of bone. A clinico-pathological study of sixty-nine cases. J. Bone and Joint Surg.,52-B(2): 205-226, 1970.52-B(2)205  1970 
     
    Simon, M. A., and Springfield, D. S.: Surgery for Bone and Soft Tissue Tumors, pp. 190-191. Philadelphia, Lippincott-Raven, 1998. 
     
    Springfield, D. S.; Capanna, R.; Gherlinzoni, F.; Picci, P.; and Campanacci, M.: Chondroblastoma. A review of seventy cases. J. Bone and Joint Surg.,67-A: 748-755, June 1985.67-A748  1985 
     
    Weatherall, P. T.; Maale, G. E.; Mendelsohn, D. B.; Sherry, C. S.; Erdman, W. E.; and Pascoe, H. R.: Chondroblastoma: classic and confusing appearance at MR imaging. Radiology,190: 467-474, 1994.190467  1994  [PubMed]
     

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    Anchor for JumpAnchor for Jump
    +Fig. 1:Radiograph showing a Codman tumor, a proximal humeral chondroblastoma, principally based in the epiphysis but extending into the metaphysis of a sixteen-year-old boy.
    Anchor for JumpAnchor for Jump
    +Fig. 2:Microphotograph showing the classic histological characteristics of a chondroblastoma. Note especially the chondroblasts and the wire-like calcification (hematoxylin and eosin, ¥ 45).
    Anchor for JumpAnchor for Jump
    +Fig. 3:Magnetic resonance image of a chondroblastoma of the proximal part of the tibia in a sixteen-year-old boy. Note the possible invasion of the subchondral bone plate and the sclerotic changes around the lesion.
    Anchor for JumpAnchor for Jump
    +Fig. 4:Computed tomography scan of a chondroblastoma of the proximal part of the humerus in a twelve-year-old girl.
    Anchor for JumpAnchor for Jump
    +Fig. 5-A:Figs. 5-A and 5-B: Radiographs showing chondroblastomas in atypical locations.
    Fig. 5-A: A large acetabular lesion in a nineteen-year-old man.
    Anchor for JumpAnchor for Jump
    +Fig. 5-B:A lesion in the calcaneus of a twenty-six-year-old man.
    Anchor for JumpAnchor for Jump
    +Fig. 6:Light microphotograph of a specimen from a chondroblastoma with an aneurysmal-bone-cyst component. Note the presence of giant cells and the chondroid component (hematoxylin and eosin, ¥ 65).
    Brien, E. W.; Mirra, J. M.; and Ippolito, V.: Chondroblastoma arising from a nonepiphyseal site. Skel. Radiol.,24: 220-222, 1995.24220  1995 
     
    Campanacci, M.: Bone and Soft Tissue Tumors: Clinical Features, Imaging, Pathology and Treatment. Ed. 2, pp. 247-264. New York, Springer, 1999. 
     
    Codman, E. A.: Epiphyseal chondromatous giant cell tumors of the upper end of the humerus. Surg., Gynec. and Obstet.,52: 543-548, 1931.52543  1931 
     
    Crim, J. R.; Gold, R. H.; Mirra, J. M.; and Eckardt, J.: Case report 748: chondroblastoma of the femur with an aneurysmal bone cyst. Skel. Radiol.,21: 403-405, 1992.21403  1992 
     
    Dahlin, D. C., and Ivins, J. C.: Benign chondroblastoma. A study of 125 cases. Cancer,,30: 401-413, 1972.30401  1972 
     
    Fechner, R. E., and Wilde, H. D.: Chondroblastoma in the metaphysis of the femoral neck. J. Bone and Joint Surg.,56-A: 413-415, March 1974.56-A413  1974 
     
    Fink, B. R.; Temple, H. T.; Chiricosta, F. M.; Mizel, M. S.; and Murphey, M. D.: Chondroblastoma of the foot. Foot and Ankle Internat.,18: 236-242, 1997.18236  1997 
     
    Huvos, A. G., and Marcove, R. C.: Chondroblastoma of bone: a critical review. Clin. Orthop.,95: 300-312, 1973.95300  1973  [PubMed]
     
    Jaffe, H. L., and Lichtenstein, L.: Benign chondroblastoma of bone. A reinterpretation of the so-called calcifying or chondromatous giant cell tumor. Am. J. Pathol.,18: 969-991, 1942.18969  1942  [PubMed]
     
    Kahn, L. B.; Wood, F. M.; and Ackerman, L. V.: Malignant chondroblastoma. Report of two cases and review of the literature. Arch. Pathol.,,88: 371-376, 1969.88371  1969 
     
    Kyriakos, M.; Land, V. J.; Penning, H. L.; and Parker, S. G.: Metastatic chondroblastoma. Report of a fatal case with a review of the literature on atypical, aggressive, and malignant chondroblastoma. Cancer,55: 1770-1789, 1985.551770  1985  [PubMed]
     
    McLeod, R. A., and Beabout, J. W: The roentgenographic features of chondroblastoma. Am. J. Roentgenol.,118: 464-471, 1973.118464  1973 
     
    Mayo-Smith, W.; Rosenberg, A. E.; Khurana, J. S.; Kattapuram, S. V.; and Romero, L. H.: Chondroblastoma of the ribs. A case report and review of the literature. Clin. Orthop.,251: 230-234, 1990.251230  1990  [PubMed]
     
    Mirra, J. M.; Ulich, T. R.; Eckardt, J. J.; and Bhuta, S.: "Aggressive" chondroblastoma. Light and ultramicroscopic findings after en bloc resection. Clin. Orthop.,178: 276-284, 1983.178276  1983  [PubMed]
     
    Riddell, R. J.; Louis, C. J.; and Bromberger, N. A.: Pulmonary metastases from chondroblastoma of the tibia: report of a case. J. Bone and Joint Surg.,55-B(4): 848-853, 1973.55-B(4)848  1973 
     
    Rodgers, W. B., and Mankin, H. J.: Metastatic malignant chondroblastoma. Am. J. Orthop.,25: 846-849, 1996.25846  1996  [PubMed]
     
    Schajowicz, F., and Gallardo, H.: Epiphysial chondroblastoma of bone. A clinico-pathological study of sixty-nine cases. J. Bone and Joint Surg.,52-B(2): 205-226, 1970.52-B(2)205  1970 
     
    Simon, M. A., and Springfield, D. S.: Surgery for Bone and Soft Tissue Tumors, pp. 190-191. Philadelphia, Lippincott-Raven, 1998. 
     
    Springfield, D. S.; Capanna, R.; Gherlinzoni, F.; Picci, P.; and Campanacci, M.: Chondroblastoma. A review of seventy cases. J. Bone and Joint Surg.,67-A: 748-755, June 1985.67-A748  1985 
     
    Weatherall, P. T.; Maale, G. E.; Mendelsohn, D. B.; Sherry, C. S.; Erdman, W. E.; and Pascoe, H. R.: Chondroblastoma: classic and confusing appearance at MR imaging. Radiology,190: 467-474, 1994.190467  1994  [PubMed]
     
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