eMedicine Specialties > Radiology > Musculoskeletal

Synovial Osteochondromatosis

Author: Johnny U V Monu, MD, Associate Professor of Radiology, University of Rochester School of Medicine, Program Director and Co-Head of Musculoskeletal Radiology, Head of Emergency Radiology, Department of Radiology, University of Rochester Strong Memorial Medical Center
Coauthor(s): Mayumi Oka, MD, Consulting Staff, Department of Radiology, University of Rochester, Strong Memorial Hospital
Contributor Information and Disclosures

Updated: Jun 21, 2007

Introduction

Background

Synovial osteochondromatosis (SOC) is a benign condition characterized by synovial membrane proliferation and metaplasia. The entity also is termed synovial chondromatosis. The synovial lining of a joint, bursa, or tendon sheath undergoes nodular proliferation, and fragments may break off from the synovial surface into the joint. There, nourished by synovial fluid, the fragments may grow, calcify, or ossify. The intra-articular fragment may vary in size from a few millimeters to a few centimeters.

The degree of calcification varies, and calcification may be seen as a few calcific specks or as foci of frankly ossified bodies. The fragments may be found free within the joint cavity, or they may be embedded within the proliferating synovium, which may extend into the surrounding soft tissues. The natural history of SOC entails gradual progression of disease, joint deterioration, and secondary osteoarthritis. Essentially, the disease is a benign process, and although studies in the literature have reported malignant transformation, this finding is decidedly unusual.

Pathophysiology

SOC is characterized by synovial membrane metaplasia, hyperplasia, and hyaline or myxoid change. The synovial lining of a joint, bursa, or tendon sheath undergoes nodular proliferation, and fragments may break off from the synovial surface into the joint. In this location, where they are nourished by synovial fluid, the fragments may grow, calcify, or ossify.

Mortality/Morbidity

Generally, SOC is a monoarticular disease that has a benign course. Several reports in the literature describe malignant transformation. The transformations occurred after several recurrences following treatment.

Sex

SOC shows a predilection of 2- to 4-fold for males over females.

Age

Individuals of all ages can be affected, but the disease is often diagnosed in persons aged 20-50 years.

Presentation

Patients with SOC often relate a history of several years of joint pain with swelling. The affected joint frequently has an associated limitation in range of motion and/or a history of locking. SOC is almost always a monoarticular process, and the large joints are more commonly affected. These include the knee, hip, elbow, and shoulder. However, the disease process may affect any synovial surface, including the extra-articular bursa.

SOC shows a predilection for males that is 2- to 4-fold greater than that for females; most patients with SOC present in the third to fifth decades of life.

If the intra-articular fragments are adequately calcified, the diagnosis is easily made with plain radiographic examination. With noncalcified fragments, magnetic resonance imaging (MRI) scans are required to show the nature and extent of SOC.

Purists differentiate primary, or idiopathic, SOC from the secondary form. In secondary SOC, the initial predisposing factor is an unrelated articular process leading to joint disintegration, production of intra-articular fragments, synovitis, and, eventually, synovial metaplasia. The cause of primary SOC is unknown.

Preferred Examination

Radiographic findings are frequently diagnostic. Computed tomography (CT) scans and CT arthrograms also may be used, especially for demonstrating noncalcified intra-articular bodies. MRI usually helps establish the diagnosis, and the images demonstrate the true extent of the disease. Ultrasonographic examination may be used to investigate accessible joints.

Radiographs should be obtained first. MRI scans should then be obtained preoperatively. When MRI is not readily available, CT arthrography may be performed.

Limitations of Techniques

Radiographs may not demonstrate noncalcified bodies. CT scans may not demonstrate the full extent of proliferating synovial disease. SOC may be confused with pigmented villonodular synovitis (PVNS) if only MRI scans are available, and plain radiographs may help in such cases.

Differential Diagnoses

Pigmented Villonodular Synovitis

Other Problems to Be Considered

Rice bodies of tuberculosis and rheumatoid arthritis 
Synovial hemangioma

More on Synovial Osteochondromatosis

Overview: Synovial Osteochondromatosis
Imaging: Synovial Osteochondromatosis
Follow-up: Synovial Osteochondromatosis
Multimedia: Synovial Osteochondromatosis
References

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Further Reading

Keywords

synovial chondromatosis, SOC, synovial membrane proliferation, synovial membrane metaplasia, synovial membrane hyperplasia, pigmented villonodular synovitis, PVNS, Rice bodies, synovial hemangioma

Contributor Information and Disclosures

Author

Johnny U V Monu, MD, Associate Professor of Radiology, University of Rochester School of Medicine, Program Director and Co-Head of Musculoskeletal Radiology, Head of Emergency Radiology, Department of Radiology, University of Rochester Strong Memorial Medical Center
Johnny U V Monu, MD is a member of the following medical societies: Radiological Society of North America
Disclosure: Nothing to disclose.

Coauthor(s)

Mayumi Oka, MD, Consulting Staff, Department of Radiology, University of Rochester, Strong Memorial Hospital
Mayumi Oka, MD is a member of the following medical societies: American College of Radiology
Disclosure: Nothing to disclose.

Medical Editor

David S Levey, MD, PhD, Orthopedic/Spine MRI TeleRadiologist, Radsource, LLC
David S Levey, MD, PhD is a member of the following medical societies: American Roentgen Ray Society, Radiological Society of North America, and Texas Medical Association
Disclosure: Nothing to disclose.

Pharmacy Editor

Bernard D Coombs, MB, ChB, PhD, Consulting Staff, Department of Specialist Rehabilitation Services, Hutt Valley District Health Board, New Zealand
Disclosure: Nothing to disclose.

Managing Editor

Javier Beltran, MD, Chair, Department of Radiology, Maimonides Medical Center
Disclosure: Nothing to disclose.

CME Editor

Robert M Krasny, MD, Consulting Staff, Department of Radiology, The Angeles Clinic and Research Institute
Robert M Krasny, MD is a member of the following medical societies: American Roentgen Ray Society and Radiological Society of North America
Disclosure: Nothing to disclose.

Chief Editor

Felix S Chew, MD, MBA, EdM, Professor, Department of Radiology, Vice Chairman for Radiology Informatics, Section Head of Musculoskeletal Radiology, University of Washington
Felix S Chew, MD, MBA, EdM is a member of the following medical societies: American Roentgen Ray Society, Association of University Radiologists, and Radiological Society of North America
Disclosure: Nothing to disclose.

 
 
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