Diagnosis: Secondarysynovialosteochondromatosisfrom osteoarthritis
Discussion: Synovial chondromatosis is benign andmay occur as either a primary or secondary form. Itis considered a metaplasia. When calcified, it is known as synovial osteochondromatosis. Malignant dedifferentiation into chondrosarcoma is rare.
Primarysynovialchondromatosisoccurs in the setting of no identifiable etiology.
Secondary synovial chondromatosis can occur from trauma, osteonecrosis, rheumatoid arthritis, neuropathic arthropathy, and tuberculous arthritis.
The underlying pathology involves loose bodies of cartilage or bone that undergo metaplasia. The bodies are slow-growing and may cause locking and pressure erosions.
Involvement is typically monoarticular, with the large joints being most frequently affected.The knee joint is involved in the majority of cases; the shoulder,elbow, and hip are the next most frequently involved joints.
On T1-weighted sequences, the bodies are higher in signal than the effusion.
On T2-weighted sequences, the bodies are lower insignal than both the subcutaneous fat and effusion.
Synovial chondromatosis can be distinguished from pigmented villous nodular synovitis (PVNS) by the lack of blooming on gradient echoimaging. PVNS is typically associated with bone erosions.
Lipomatous arborescens, which are intra-articular areas of fat signal, may also mimic synovial chondromatosis.The aggressive nature ofsynovial sarcoma and chondrosarcoma typically preclude themselves from the differential diagnosis.