Lateral Knee Pain in a Male College Student
Am Fam Physician. 2012 Mar 1;85(5):509-510.
A 20-year-old man presented to his university's student health clinic with intermittent pain in his right knee that began two months earlier. He had no history of knee injury or surgery and was otherwise in good health.
Physical examination showed a visually normal knee with no effusion. He had normal range of motion but slight tenderness to palpation over the lateral femoral condyle. Testing of the medial and lateral collateral ligaments showed no laxity, and the iliotibial band was not tight. Radiography of the knee was performed (see accompanying figure).
Based on the patient's history, physical examination and radiographic findings, which one of the following is the most likely diagnosis?
A. Giant cell tumor of bone.
B. Myositis ossificans.
C. Nonossifying fibroma.
D. Osteoid osteoma.
The answer is E: osteosarcoma. Osteosarcomas are common primary malignant bone tumors, with more than 2,400 new cases annually in the United States. Although osteosarcomas can occur at any age, 75 percent of patients with the condition are in adolescence to early 20s. It is more common in males than in females, with a male-to-female ratio of 1.6:1.1 The typical presentation includes mild or intermittent pain around the involved area. As the tumor increases in size, pain intensifies and swelling may be appreciated. Although osteosarcomas can occur in any metaphyseal area of long bones, the distal femur or proximal tibia is the most common location, followed by the proximal humerus.2
The patient's radiograph demonstrates mixed lytic and blastic features with cortical destruction along the lateral femoral condyle, which are typical findings in osteosarcoma.2 Radiographs often show medullary and cortical destruction with a sunburst or velvety appearance of neoplastic bone along the periosteum. Codman triangle (a triangular shadow between the cortex and raised periosteum) may also be present.3
Osteosarcoma is an aggressive neoplasm, with metastasis in 20 percent of patients at the time of diagnosis. Patients without metastases have a five-year survival rate of 80 percent.4
Giant cell tumors of bone are uncommon, nonmalignant, locally aggressive tumors that occur after skeletal maturity. They are more common in women.1 Giant cell tumors develop in the epiphysis of long bones, most commonly in the distal femur or proximal tibia. Radiographs typically show a large eccentric, osteolytic lesion extending into the soft tissue.2
Myositis ossificans is a benign reactive ossification process within muscle tissue, usually following trauma. Most lesions occur along the femur in adolescent athletes. The key radiologic feature is the “zonal phenomenon,” with radiolucent immature bone in the center of the lesion and mature radiodense bone at the periphery.3
Nonossifying fibromas are the most common bony lesions in children and adolescents.2 Most are asymptomatic, incidental findings on radiography. Radiographs show elliptical radiolucent lesions with sclerotic borders in the cortex of long bones near the growth plates. These lesions are not neoplasms, and most resolve spontaneously with skeletal maturity. Large and progressive lesions that involve more than 50 percent of the medullary cavity are prone to pathologic fracture.2
Osteoid osteomas are benign neoplasms that primarily occur in adolescence or the early 20s, and are more common in males.3 Osteomas usually develop in the proximal femur and tibia. Radiographs show a well-circumscribed, 1- to 2-cm lesion with a central osteoblastic area or “nidus” surrounded by a sclerotic border.2 Clinically, pain is more severe at night and relieved with aspirin or other nonsteroidal anti-inflammatory drugs.3
Giant cell tumor of bone
Large eccentric, osteolytic lesion may extend into adjacent soft tissue, develops in the epiphysis of long bones, most commonly in the distal femur or proximal tibia
Ossification process within muscle tissue following trauma, most common along the femur in adolescent athletes
Elliptical radiolucent lesions with sclerotic borders in the cortex of long bones near the growth plates, most common bony lesion in children and adolescents
Well-circumscribed, 1- to 2-cm lesion with central osteoblastic area or “nidus” with a sclerotic border, most common in the proximal femur and tibia, primarily occurs in adolescence to early 20s
Mixed lytic and blastic lesion in metaphyseal area of long bones, most commonly the distal femur or proximal tibia; sunburst or velvety appearance of neoplastic bone along periosteum, usually occurs when patients are in adolescence to early 20s
1. Robbins SL, Kumar V, et al., eds. Robbins Basic Pathology. 8th ed. Philadelphia, Pa.: Saunders/Elsevier; 2007.
2. Greenspan A. Orthopedic Radiology: A Practical Approach. 3rd ed. Philadelphia, Pa.: Lippincott Williams & Wilkins; 2000.
3. Rubin R, Strayer DS. Rubin's Pathology: Clinicopathologic Foundations of Medicine. 5th ed. Philadelphia, Pa.: Lippincott Williams & Wilkins; 2008.
4. Wittig JC, Bickels J, Priebat D, et al. Osteosarcoma: a multidisciplinary approach to diagnosis and treatment. Am Fam Physician. 2002;65(6):1123–1132.
Contributing editor for Photo Quiz is John E. Delzell, Jr., MD, MSPH.
A collection of Photo Quizzes published in AFP is available at http://www.aafp.org/afp/photoquiz.
The editors of AFP welcome submissions for Photo Quiz. Guidelines for preparing and submitting a Photo Quiz manuscript can be found in the Authors' Guide at http://www.aafp.org/afp/photoquizinfo. To be considered for publication, submissions must meet these guidelines. E-mail submissions to email@example.com.
Copyright © 2012 by the American Academy of Family Physicians.
This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP. Contact firstname.lastname@example.org for copyright questions and/or permission requests.
Want to use this article elsewhere? Get Permissions