El Mandour Jihane, Khouchoua Selma, Adjou Nada, El Haddad Siham, Allali Nazik, Chat Latifa
Department of Radiology, Mother and Child Hospital, CHU IBN SINA, Rabat, Morocco.
Radiol Case Rep. 2023 Aug 5;18(10):3652-3656. doi: 10.1016/j.radcr.2023.07.042. eCollection 2023 Oct.
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.
奥利尔病是一种罕见疾病，其特征为多发内生软骨瘤以及软骨病变的不对称分布，这些病变在大小、位置、年龄和性别上差异显著。该病的主要症状是在短骨或长骨的干骺端出现非骨化性软骨细胞团或错构瘤样软骨细胞生长。特定病例可能进展为软骨肉瘤或骨肉瘤。X线是骨骼疾病最基本的诊断技术。在本文中，我们介绍了摩洛哥拉巴特伊本·西那母子医院的一例奥利尔病病例。
