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Secondary synovial chondromatosis is the more common form and often occurs when there is pre-existent osteoarthritis, rheumatoid arthritis, osteonecrosis, osteochondritis dissecans, neuropathic osteoarthropathy (which often occurs in diabetic individuals), tuberculosis, or osteochondral fractures (torn cartilage covering the end of a bone in a ...
Synovial osteochondromatosis (SOC) (synonyms include synovial chondromatosis, primary synovial chondromatosis, synovial chondrometaplasia) is a rare disease that creates a benign change or proliferation in the synovium or joint-lining tissue, which changes to form bone-forming cartilage. In most occurrences, there is only one joint affected ...
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Tenosynovial giant cell tumor is a type of benign tumor that affects the lining of joints and tendons.
Synovial chondromatosis occurs in a much older age group and can be ruled out on this basis. [2] Treatment. Most reported cases of DEH in the literature have been ...
Synovial chondromatosis can be confidently diagnosed by X-ray when calcified cartilaginous chondromas are seen. However, other synovial proliferative processes, such ...
Patrick's test or FABER test is performed to evaluate pathology of the hip joint or the sacroiliac joint. [1]The test is performed by having the tested leg flexed and the thigh abducted and externally rotated.
Familial synovial chondromatosis with dwarfism is a rare genetic disorder characterized by a combination of both synovial chondromatosis and dwarfism. [ 1 ] [ 2 ] Only 3 families from Germany and the United States worldwide have been described with the disorder, and they showed either X-linked or autosomal dominant inheritance.