eMedicine Specialties > Orthopedic Surgery > Neoplasms

Cartilage Tumors, Low Grade

Author: Anthony E Johnson, MD, Chief, Department of Specialty Care, Chief, Orthopaedic Surgery and Podiatry Service, Specialty Care, McDonald Army Hospital
Coauthor(s): Josefine M Heim-Hall, MD, Clinical Associate Professor, Department of Pathology, University of Texas Health Science Center at San Antonio; Ronald P Williams, MD, PhD, Chair, Department of Orthopedics, University of Texas Health Science Center at San Antonio
Contributor Information and Disclosures

Updated: May 8, 2008

Introduction

Cartilage tumors vary in severity from benign enchondroma to low-grade malignant chondrosarcoma to the highest-grade dedifferentiated chondrosarcoma. Chondrosarcoma is the second most common primary malignant bone tumor, accounting for 10-20% of all primary bony malignancies.^1,2 Enchondroma, which consists of benign endosteal cartilage, is much more common than chondrosarcoma. The true incidence of cartilage tumors is unknown because many are discovered incidentally. Distinguishing benign cartilage tumors from low-grade malignant cartilage tumors is often challenging, but there are some established principles regarding location, size, and pain, as well as characteristics on radiography, computed tomography (CT), and magnetic resonance imaging (MRI).^3,4,5,6,7

• Location: Most cartilage tumors of the hands and feet are benign, whereas cartilage tumors of the pelvis, scapula, and sternum are more likely to be malignant.⁸
• Size: Most enchondromas are smaller than 3 cm; benign tumors larger than 5 cm are uncommon.
• Pain: Both benign and malignant cartilage tumors may be associated with pain. However, a careful history characterizing the pain may help distinguish pain due to arthrosis of an adjacent joint or other causes of limb pain from pain associated with an underlying bone lesion. If an injection in the adjacent joint completely relieves the pain, the associated bone lesion is a doubtful source of symptoms.
• Radiographic features: Radiographs are crucial in distinguishing chondrosarcomas from enchondromas. Enchondromas are usually radiographically well marginated and are much more likely to demonstrate the characteristic punctate or flocculent intralesional mineralization pattern that is the hallmark of calcified hyaline cartilage. Enchondromas may also cause expansion of the cortex, especially in flat bones. More extensive endosteal erosion, especially involving greater than one half to two thirds the width of the cortex, should increase suspicion of malignancy, whereas frank cortical destruction and soft tissue extension should be considered evidence of malignancy.
• Computed tomography: CT scanning is particularly useful in evaluating the relationship of an endosteal cartilage tumor to the adjacent cortex. An enchondroma is expected to have an intact rind of cortical bone surrounding it.⁹
• Magnetic resonance imaging: MRI signal characteristics, such as increased signal intensity on T2-weighted images, heterogeneity of the matrix, and lack of intralesional mineralization, are suggestive of malignancy.

Even with optimal clinical, radiographic, and histologic data, there is often no clear distinction between benign and low-grade malignant cartilage tumors.^1,10,11,12 This distinction is particularly difficult with very low grade chondrosarcomas, or so-called borderline chondrosarcomas. These cartilage tumors have cytology resembling enchondromas; cortical erosions or scalloping without frank full-thickness cortical destruction visible on plain radiographs; clinical presentation of intermittent to constant pain; and local recurrences similar to those of low-grade chondrosarcomas.^13,14 Low-grade malignant chondrosarcomas, which constitute the majority of malignant cartilage tumors, have been described as having a slow growth rate, infrequent metastases, and a 90% 5-year survival rate.^1,2,15

In addition to the conventional intramedullary tumors, both benign and malignant cartilage tumors may be found in periosteal locations or in soft tissue. Secondary chondrosarcomas may arise in an osteochondroma, in an enchondroma, or in the setting of enchondromatosis (Ollier disease or Maffucci syndrome) or multiple osteochondromatosis. The secondary chondrosarcomas are more likely to occur in patients with multiple cartilage tumors and typically present as a painful, progressively enlarging bony mass. Dedifferentiated chondrosarcoma is a distinct subgroup of chondrosarcoma in which a high-grade noncartilaginous sarcoma is adjacent to either a low-grade chondrosarcoma or enchondroma.

Lee et al monitored 227 patients with chondrosarcoma for an average of 6 years and reported predictive factors for metastasis to be local recurrence, pelvic location, tumor volume greater than 100 cc, aneuploidy of the tumor coupled with a high mean DNA index, histologic grade 3, and dedifferentiated chondrosarcomas. The reported recurrence rate ranges from 4-12%, depending on initial treatment modality and tumor grade.^16,17

Classically, because chondrosarcomas are known to be resistant to radiotherapy and chemotherapy, wide resection has generally been accepted as recommended treatment for low-grade chondrosarcoma.^18,19,20,21 Borderline cartilage tumors have an even lower metastatic potential than the true low-grade (grade 1) malignant chondrosarcoma.^9,13 Thus, recommended treatment of these borderline tumors has ranged from marginal curettage and grafting to limited local resection. There has been a push for more conservative treatment of borderline and low-grade malignant chondrosarcomas, with extended intralesional curettage being considered a viable alternative to wide resection.^9,13,14

Related Medscape topics:
Specialty Site Orthopaedics
Specialty Site Oncology
Resource Center Cancer: Biologic Therapies
Metastases or Osteoma?

Case Studies

The following discussion is a description of 2 cases that initially presented as clinically, radiographically, and pathologically borderline cartilage tumors and eventually demonstrated aggressive metastatic behavior, as well as a third case in which a radiographically and histologically benign enchondroma was detected only after it had undergone dedifferentiation into a high-grade osteosarcoma and resulted in a pathologic fracture. Case 1

A 38-year-old female athlete presented with a minimally painful lump on the medial side of her left knee (see Image 1). She underwent open biopsy with curettage later that same month. Histology at that time showed benign enchondroma with focal atypia (see Image 2). The patient developed a recurrence of the mass 19 months later. She underwent augmented (phenol) marginal resection 2 months after the recurrence, after refusing wide resection. Histology showed progression from a purely low-grade to a mixed low- and intermediate-grade lesion (ie, chondrosarcoma grade 1-2 of 3 [see Image 3]).

One year after the first recurrence, she developed a second recurrence and underwent wide resection and reconstruction of the distal femur. The tumor within the distal femur was a high-grade dedifferentiated chondrosarcoma with osteosarcomatous features (see Image 4). She then underwent adjuvant chemotherapy for osteosarcoma.

Five months after the second recurrence, she developed lung metastases. Biopsy of the lung lesions revealed dedifferentiated chondrosarcoma. One month later, she developed a recurrence of the high-grade sarcoma in the popliteal fossa. The patient underwent above-knee amputation and died of progression of the lung metastases 1 year later.

A 39-year-old man presented with anterior bowing of his right femur and a leg-length discrepancy. At age 16 years, he had undergone an osteotomy to correct the angular deformity. Plain radiography of the right distal femur revealed a cartilage tumor in the distal femur. MRI demonstrated disruption of the anterior femoral cortex, with thinning of the articular cartilage. The patient underwent curettage and bone grafting. Histologic examination revealed a well-differentiated cartilaginous tumor, and a diagnosis of benign enchondroma was favored (see Image 5). The original osteotomy was apparently through the enchondroma (see Image 6).

The patient reported recurrent knee pain 20 months after curettage and bone grafting and underwent repeat curettage. The histology showed progression to grade 2 chondrosarcoma (see Image 7). Follow-up CT scan showed a lytic lesion in the posterior femoral condyle extending to the distal femoral joint line. He underwent wide resection with distal femoral replacement 2 months later. The histologic examination confirmed grade 2 chondrosarcoma.

Thirteen months later, CT scanning of the chest revealed approximately 20 small pulmonary nodules. The resected lung nodules all revealed grade 2 chondrosarcoma histologically identical to the tumor excised from the distal femur (see Image 8). The patient initiated chemotherapy. Six months later, he had multiple enlarging nodules but remained asymptomatic, and he refused further treatment.

A 70-year-old man sustained a right supracondylar femur fracture after stepping out of the bathtub. Incisional biopsy of the fracture site was performed. Histologic examination revealed a high-grade osteosarcoma with soft tissue extension sharply juxtaposed to an enchondroma (see Image 9). He underwent right hip disarticulation 1 week later. He declined chemotherapy. Lung nodules appeared on chest radiography 2 months postoperatively. CT scanning confirmed the presence of multiple pulmonary nodules consistent with metastases.

Discussion

Differentiation of benign active and low-grade (grade 1) malignant cartilaginous lesions is difficult. Recent diagnostic schemata have included a borderline category of cartilage tumors.^13,14 Some authors have supported a more conservative intralesional curettage with or without surgical adjuvant therapy (such as liquid nitrogen or phenol) as effective therapy for these borderline tumors. Although the overall recurrence rate of low-grade chondrosarcoma is low, a substantial proportion of the recurrent tumors manifest themselves at a higher histologic grade than their corresponding primary tumors. The reported frequency of this recurrence varies in the literature but may be as high as 61%.¹⁷

Case 1 and Case 2 are examples of grade progression from a borderline tumor to a grade 2 chondrosarcoma. Both patients underwent limited resection of their original borderline chondrosarcomas, but the disease recurred as higher-grade tumors at 19 and 20 months from initial presentation, respectively. The patient in Case 1 refused wide resection at recurrence and eventually developed lung metastases after dedifferentiation at the primary site. Whether this poor outcome could have been prevented with wide resection of the recurrent tumor is unknown. The patient in Case 2, on the other hand, did undergo wide resection of recurrent tumor, but metastasis occurred nevertheless. Although both cases underscore the need for wide resection of the recurrent chondrosarcoma, the second case questions the safety of conservative management for borderline chondrosarcoma.

Case 3 is an example of what appeared to be a solitary benign enchondroma that dedifferentiated into a high-grade osteosarcoma. This is a rare event, with only a few cases reported in the literature.²² Although wide excision would not be the recommended treatment for a benign enchondroma, this case serves as another example of an unusually aggressive cartilage tumor.

Conclusion

Currently, no prospective, controlled studies describe the appropriate treatment for borderline or low-grade (grade 1) malignant chondrosarcomas. Some authors have suggested that extended intralesional curettage may be acceptable for both types. However, limited resection was clearly insufficient to control borderline cartilage tumors in the case studies described above and resulted in an unexpectedly poor outcome. Caution should be utilized both in making the distinction between benign and malignant cartilage tumors and in selecting the appropriate surgical treatment for grade I chondrosarcomas.

Multimedia

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Media file 1: Original MRI of a patient demonstrating a lesion extending beyond the boundary of normal bone.

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Media file 2: Histology of original lesion demonstrating what was thought to be a benign enchondroma with some atypical features.

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Media file 3: Recurrent tumor demonstrating progression from a purely low-grade lesion to a mixed low- and intermediate-grade lesion.

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Media file 4: Tumor from distal femur at time of reconstruction demonstrating dedifferentiated chondrosarcoma.

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Media file 5: Tumor from pin sites revealing a well-differentiated cartilaginous tumor. The diagnosis of benign enchondroma was favored at this point.

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Media file 6: AP radiograph of the knee demonstrating a tumor around screw holes.

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Media file 7: Histology at time of recurrence showing progression to grade 2 chondrosarcoma.

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Media file 8: Histology showing grade 2 chondrosarcoma within lung metastases. This tumor was identical to the tumor resected from the distal femur.

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Media file 9: Histology at fracture site demonstrating sharp juxtaposition of benign enchondroma with osteosarcoma.

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Media file 10: This patient has an enchondroma. Radiography typically shows well-defined, sharply marginated medullary lesions, often with punctate ring and arclike calcifications. Bone infarcts may appear similar to enchondromata on plain radiography. CT scanning is recommended to evaluate the extent of endosteal scalloping.

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Media file 11: This patient has a chondrosarcoma. The MRI demonstrates a lesion in the proximal humerus, with extension through the cortex into the soft tissues. The distinction between enchondroma and chondrosarcoma is extremely difficult, even with complete radiographic and histopathologic evaluation.

Keywords

chondrosarcomas, enchondromas, osteosarcoma, multiple enchondromatosis, Ollier disease, Ollier's disease

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