Orthopedic Basic 2026 MCQs (Part 2): Fracture Healing, Bone Tumors & Joint Anatomy Board Review

Multidisciplinary treatment combining systemic chemotherapy and adequate surgical resection has resulted in a 5-year survival rate of 70% in patients with nonmetastatic osteosarcoma of the extremity . The advent of effective chemotherapy has increased the overall survival rate from 20% to 70% in current studies. Arndt CA, Crist WM: Common musculoskeletal tumors of childhood and adolescence. N Engl J Med 1999;341:342-352.

16b 16c 16d 16e The imaging studies are consistent with a chondrosarcoma. The radiograph shows a radiolucent lesion in the pelvis, and there are stippled calcifications on the CT scan. The histology shows a low-grade cellular hyaline cartilage neoplasm with stellate, occasionally binucleated chondrocytes. Enchondroma has a more benign histologic appearance.

17b 17c The patient has a Charcot arthropathy of the knee, which is associated with amyloidosis. The rapid joint destruction shown in the radiographs is most consistent with that diagnosis. Drennan D, Fahey J, Maylahn D: Important factors in achieving arthrodesis of the Charcot knee. J Bone Joint Surg Am 1971;53:1180-1193. Soudry M, Binazzi R, Johanson N, et al: Total knee arthroplasty in Charcot and Charcot like joints. Clin Orthop 1986;208:199-204.

The grading of response to chemotherapy for osteosarcoma was introduced by Huvos and associates. Patients with tumors that show more than 90% necrosis after neoadjuvant chemotherapy are considered to have had a good response and have better survival rates than those with less than 90% necrosis. However, it should be noted that survival rates for patients with a poor response are still better than in patients who do not receive neoadjuvant chemotherapy. More recently, similar results have been reported in patients with Ewing's sarcoma. Chemotherapy is not typically used for giant cell tumor of bone. Meyers PA, Heller G, Healey J, Huvos A, Lane J, Marcove R, et al: Chemotherapy for nonmetastatic osteogenic sarcoma: The Memorial Sloan- Kettering experience. J Clin Oncol 1992;10:5-15.

The work-up for a patient with an unknown primary lesion that is metastatic to bone includes a search for the primary tumor and other sites of metastasis. This involves conducting a thorough history and physical examination, appropriate laboratory studies, bone scan, chest radiograph, and CT of the chest, abdomen, and pelvis. In women, a mammogram may be indicated. CT of the brain is not necessary in the early stages of a metastatic work-up. Simon MA, Bartucci EJ: The search for the primary tumor in patients with skeletal metastases of unknown origin. Cancer 1986;58:1088-1095.

18b 18c The radiographic appearance of the lesion is lytic with calcifications in the supra-acetabular region. The CT scan shows bone destruction and periosteal reaction, which rules out an enchondroma. The histologic appearance is that of cellular cartilage, with a high cytoplasmic:nuclear ratio and basophilic appearance to the cytoplasm; these findings rule out chordoma and metastatic renal cell carcinoma. In addition, chordomas are most frequently found in the sacrum and base of the skull. Because there is no high-grade spindle cell component to suggest dedifferentiation, the most likely diagnosis is chondrosarcoma. Pring M, Weber KL, Unni K, Sim FH: Chondrosarcoma of the pelvis: A review of sixty-four cases. J Bone Joint Surg Am 2001;83:1630-1642.

The most common malignant disease to arise in conjunction with chronic osteomyelitis is squamous cell carcinoma particularly in patients with a long-standing draining sinus tract. Dell PC: Hand, in Simon MA, Springfield D (eds): Surgery for Bone and Soft Tissue Tumors. Philadelphia, PA, Lippincott-Raven, 1998, pp 405-420.

19b 19c The radiograph shows a calcified lesion in the medullary canal of the distal femoral diaphysis. The MRI scan shows extensive marrow change distal to the lesion, which is not consistent with an enchondroma. The histology shows a biphasic pattern with low-grade cartilage just apposed to high-grade spindle cell sarcoma. The overall appearance is consistent with dedifferentiated chondrosarcoma. The radiographic appearance is not consistent with enchondroma, and the histologic appearance is not consistent with the other choices. Mitchell AD, Ayoub K, Mangham DC, et al: Experience in the treatment of dedifferentiated chondrosarcoma. J Bone Joint Surg Br 2000;82:55-61.

20b 20c 20d Based on these findings, the most likely diagnosis is fibrous dysplasia. Twenty percent of patients with fibrous dysplasia have multifocal disease. The lesions show a typical ground glass appearance. Fibrous dysplasia frequently involves the diaphysis of the long bones. There is no associated soft-tissue mass and no periosteal reactions to these lesions, suggesting a benign lesion. The histology shows proliferating fibroblasts in a dense collagen matrix. Trabeculae are arranged in an irregular or "Chinese letter" appearance. Osteogenic sarcoma and Ewing's sarcoma have a much different radiographic appearance of malignant osteoid and small round blue cells. Periosteal chondroma does occur in the proximal humerus but is not typically multifocal. It appears as a surface lesion with saucerization of the underlying bone and a bony buttress adjacent to the lesion. Some patients with multifocal lesions have associated endocrine abnormalities (McCune-Albright syndrome). Wold LA, et al: Atlas of Orthopaedic Pathology. Philadelphia, PA, WB Saunders, 1990, pp 118-119.

Following excision of a suspected benign soft-tissue tumor that proves to be malignant, repeat excision of the tumor bed is recommended. The initial surgical margins are inadequate after an intralesional or marginal excision, necessitating additional surgery for more definitive local control. While radiation therapy and/or chemotherapy may help to reduce the risk of local recurrence in patients with microscopic residual disease, local control is improved following repeat excision. Radiation therapy alone is inadequate to address poor surgical margins, and would likely be given postoperatively. Bisphosphonates have no current role in the treatment of soft-tissue sarcoma. Noria S, Davis A, Kandel R, et al: Residual disease following unplanned excision of soft-tissue sarcoma of an extremity. J Bone Joint Surg Am 1996;78:650-655.

Most soft-tissue sarcomas are treated with a combination of radiation therapy and wide resection. Rhabdomyosarcomas are an exception, where chemotherapy is included in all treatment plans. Chemotherapy for other soft-tissue sarcomas is controversial. Enzinger FM, Weiss SW: Rhabdomyosarcoma, in Soft Tissue Tumors, ed 3. St Louis, MO, CV Mosby, 1995, p 539.

21b The radiographs show an eccentric metaphyseal lesion with a well-defined reactive rim of bone that is consistent with a nonossifying fibroma. Pathologic fractures through benign lesions should be treated as appropriate for the fracture, allowing the fracture to heal. Biopsy is not needed when the radiographic diagnosis is benign. MRI, in the presence of a fracture, is not particularly helpful because of the hematoma. If radiographic findings reveal that the lesion appears aggressive, a biopsy should be performed, obtaining tissue away from the fracture site. Marks KE, Bauer TW: Fibrous tumors of bone. Orthop Clin North Am 1989;20:377.

22b Gouty arthritis, pseudogout, and infection can all present with inflammatory arthritis and periarticular erosions. Strongly negative birefringent crystals are seen in gout. The histologic image shows elongated "needle-like" crystals of gout. Epidermal inclusion cysts are rarely painful and usually have a history of localized penetrating trauma. Hamilton W, Breedman KB, Haupt HM, Lackman R: Knee pain in a 40-year-old man. Clin Orthop 2001;383:282-285,290-292.

Most lesions of eosinophilic granuloma are simply observed, but larger aggressive lesions may require curettage and bone grafting. Frequently, biopsy is required to rule out a malignant diagnosis. The differential diagnosis of eosinophilic granuloma is osteomyelitis, Ewing's sarcoma of bone, or osteogenic sarcoma. The biopsy alone can be followed by spontaneous resolution. In some patients, low-dose radiation therapy is used. Chemotherapy or amputation is not indicated for these benign lesions.

23b 23c 23d 23e 23f The histology shows cells with bubbly, abundant clear cytoplasm typical of physaliphorous cells; therefore, the most likely diagnosis is chordoma. These tumors arise from notocord rests in the upper and lower spine.

The radiograph shows an aggressive destructive lesion. In this age group, and based on the anatomic location, a primary malignant tumor (osteosarcoma) is likely. Additional staging studies to identify metastatic disease are imperative prior to any biopsy. MRI of the femur helps to reveal skip metastasis and provides information regarding the anatomic location of the lesion. CT of the chest and a bone scan evaluate for distant metastatic spread. A bone scan is also useful in evaluating the extent of local bone activity about the lesion. Simon MA, Finn HA: Diagnostic strategy for bone and soft tissue tumors. J Bone Joint Surg Am 1993;75:622-631.

Osteosarcoma is the most common primary malignant tumor of bone in childhood, followed by Ewing's sarcoma. Rhabdomyosarcoma is a soft-tissue sarcoma of childhood. Chondrosarcoma rarely occurs in childhood. Osteochondromas are benign tumors of the bone. Simon M, Springfield D, et al: Osteogenic Sarcoma: Surgery for Bone and Soft Tissue Tumors. Philadelphia, PA, Lippincott Raven, 1998, p 226.

The patient underwent a wide resection, which involves excision of the tumor along with a cuff of normal tissue that completely surrounds the tumor. The plane of resection is beyond the reactive zone. A radical resection involves removal of the entire affected muscle from origin to insertion. In a marginal excision, the plane of dissection is through the reactive zone of the tumor. A marginal excision is generally considered inadequate surgery for high-grade sarcomas. In an intralesional resection, the plane of dissection is through the tumor. Excision within the reactive zone but beyond the tumor is the same as a marginal excision. Enneking WF: Staging of musculoskeletal neoplasms, in Current Concepts of Diagnosis and Treatment of Bone and Soft Tissue Tumors. Heidelberg, Germany, Springer-Verlag, 1984.

In nearly 50% of patients with a unicameral bone cyst, the lesion remains asymptomatic until a fracture occurs, usually as the result of relatively minor trauma. If the lesion expands, the bone is weakened and may cause pain. Fibrous cortical defects are usually an incidental finding and typically asymptomatic. Malignant bone tumors such as osteosarcoma and Ewing's sarcoma most commonly cause pain, and pathologic fracture occurs in less than 10% of patients. Giant cell tumors are uncommon in children and usually are painful. Wilkins RM: Unicameral bone cysts. J Am Acad Orthop Surg 2000;8:217-224. Dormans JP, Pill SG: Fractures through bone cysts: Unicameral bone cysts, aneurysmal bone cysts, fibrous cortical defects, and nonossifying fibromas. Instr Course Lect 2002;51:457-467.

25b The clinical history, CT scan, and histology are most consistent with a lymphoma of bone. An important part of the staging is bone marrow aspiration and biopsy. The other studies listed are not indicated. Lymphoma of bone, when localized, is usually treated with chemotherapy and radiation therapy and has excellent survival rates. Widespread lymphoma has a worse prognosis. Finiewicz K, van Biesen K: Non-Hodgkins lymphoma, in Golomb H, Vokes E (eds): Oncologic Therapies, ed 2. Berlin, Germany, Springer, 2003, pp 295-318.

The use of multiagent chemotherapy has been shown to be associated with a survival benefit in patients with osteosarcoma. The use of chemotherapy in adults with soft-tissue sarcoma remains somewhat controversial. It has not been associated with improved survival rates in patients with renal carcinoma, dedifferentiated chondrosarcoma, or melanoma. Menendez LR (ed): Orthopaedic Knowledge Update: Musculoskeletal Tumors. Rosemont, IL, American Academy of Orthopaedic Surgeons, 2002, p 53.

The venous plexus was described by Batson and helps to explain the common distribution of metastatic cells to the vertebrae, skull, ribs, and proximal long bones. Batson studied the vertebral vein system extensively by using contrast agents in human cadavers and live monkeys. Batson's plexus is a valveless system that allows retrograde embolism from the major organs such as the breast, prostate, lung, kidney, and thyroid. It is located within the thoracoabdominal cavity and has connections to the proximal long bones and an intercommunicating network of thin-walled veins with a low intraluminal pressure. Batson OV: Function of vertebral veins and their role in spread of metastases. Ann Surg 1940;112:138-149.

The lesion has the typical "blown out" lytic radiographic appearance that is most commonly found in thyroid or renal cell metastases. Given the history of hematuria and histology findings, the most likely diagnosis is metastatic renal cell carcinoma. This tumor is relatively resistant to chemotherapy. Radiation therapy is used as a postoperative adjuvant treatment with varying response rates. Surgery should be performed after preoperative embolization to decrease the risk of intraoperative bleeding, as no tourniquet can be used in this location. Patients with metastatic renal cell carcinomas may survive for years, resulting in a higher likelihood of local tumor progression with ineffective adjuvant therapy. Intramedullary fixation combined with curettage and cementation will provide the best chance of local control while maintaining the patient's native shoulder and elbow joints. A total humeral resection is an extensive surgery with considerable morbidity and is not indicated for this patient because less extensive surgery is likely to be effective. Harrington KD, Sim FH, Enis JE, Johnston JO, Diok HM, Gristina AG: Methylmethacrylate as an adjunct in internal fixation of pathological fractures: Experience with three hundred and seventy-five cases. J Bone Joint Surg Am 1976;58:1047-1054. Sun S, Lang EV: Bone metastases from renal cell carcinoma: Preoperative embolization. J Vasc Interv Radiol 1998;9:263-269.

27b 27c 27d The patient has an aneurysmal bone cyst. The fluid-fluid levels seen on the MRI scan are typical for aneurysmal bone cyst, and the histology is consistent with a cystic lining. Vascular lakes, multinucleated giant cells, reactive bone, fibrovascular tissue, and an absence of atypical cells or numerous mitoses are seen histologically. Aneurysmal bone cysts will typically continue to grow and cause further bone destruction; therefore, observation is not recommended. Steroid injections are not effective. A thorough curettage of the cyst lining and bone grafting are required. Wide resection and chemotherapy are reserved for more aggressive tumors. There is no evidence of infection radiographically or histologically. Telangiectatic osteosarcoma should also be considered in the differential diagnosis; therefore, biopsy is an important part of the work-up. Wold LA, et al: Atlas of Orthopaedic Pathology. Philadelphia, PA, WB Saunders, 1990, pp 232-233.

28b The radiograph and MRI scan reveal a lytic lesion in the left femoral neck region that extends to the lesser trochanter. Although external beam radiation and radioactive iodine infusion may be helpful in controlling the local disease, the patient is at high risk for femoral neck fracture given the location of the lesion. Prophylactic surgery is indicated; therefore, the treatment of choice is a cemented bipolar hemiarthroplasty. The use of a compression hip screw and side plate or an intramedullary nail has a high likelihood of failure with disease progression. Postoperative treatment with radiation therapy and bisphosphonates is also indicated. Mirels H: Metastatic disease in long bones: A proposed scoring system for diagnosing impending pathologic fractures. Clin Orthop 1989;249:256-264. Swanson KC, Pritchard DJ, Sim FH: Surgical treatment of metastatic disease of the femur. J Am Acad Orthop Surg 2000;8:56-65.