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Published on: September 20, 2018
Ollier disease: A case report and literature review
Jihane El Mandour1, Selma Khouchoua1, Nada Adjou1
1Department of Radiology, Mother and Child Hospital, CHU IBN SINA, Rabat, Morocco.
Abstract:
Ollier disease is an uncommon disease characterized by several enchondromas and an asymmetric distribution of cartilage lesions, which can vary significantly in size, location, age, and gender. The primary symptom of this condition is a nonossifying chondrocyte mass or hamartomatous chondrocyte growth in the metaphysis of a short or long bone. Specific cases can progress to chondrosarcoma or osteosarcoma. X-ray is the most fundamental diagnostic technique for skeletal illnesses. In this article, we present a case of Ollier disease from Mother and Child Hospital IBN SINA, Rabat, Morocco.
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