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Ollier disease: A case report and literature review
2021
World Academy of Sciences Journal
Ollier disease, also known as multiple enchondromatosis, is a rare congenital disease of unknown etiology. The main manifestation of this disease is a non-ossifying chondrocyte mass or hamartomatous growth of a chondrocyte in the metaphysis. A few cases can develop into chondrosarcoma or osteosarcoma. The present study describes the case of a 37-year-old male patient with left hip pain and dyskinesia diagnosed with Ollier disease, according to clinical features and findings of imaging analysis.
doi:10.3892/wasj.2021.106
fatcat:mljzo75qnfbpxkuc4nw7yii6ni