Ollier disease: A case report and literature review

Ollier disease, also known as multiple enchondromatosis, is a rare congenital disease of unknown etiology. The main manifestation this non‑ossifying chondrocyte mass or hamartomatous growth in the metaphysis. A few cases can develop into chondrosarcoma osteosarcoma. present study describes case 37‑year‑old male patient with left hip pain and dyskinesia diagnosed according to clinical features findings imaging analysis. In general, incidence low, thus, it not well‑known among orthopedic surgeons. However, due its malignant transformation rate, medical practitioners should encourage patients undergo regular follow‑up examinations. an aim provide some insight begins by describing affected subsequently presents review relevant literature order guide diagnosis treatment disease.