Dhemesh Yaseen, Tawekji Talha, Abdul-Baki Mohammad-Nasan, Abi-Zamr Ghazal, Ali Sawssan
Faculty of Medicine, University of Hama, Hama, Syria.
Unit of Dermatology, Children's University Hospital of Damascus, Damascus, Syria.
Oxf Med Case Reports. 2020 Jan 31;2020(1):omz145. doi: 10.1093/omcr/omz145. eCollection 2020 Jan.
Ollier disease is a rare nonhereditary skeletal disorder, characterized by multiple enchondromas, which are noncancerous growth of cartilage. In this report, we present a case of Ollier disease in a 10-year-old Syrian boy. The patient presented with multiple boney masses on hands; he had a history of pathological fractures when he was 5, which caused crippling. We analyzed the clinical, radiographical and pathological characteristics of our patient, which helped us to reach the final diagnosis. Ollier disease is a benign bone tumor, but it has a risk of malignant transformation into chondrosarcoma. The aim of this report is to document the presence of Ollier disease in Syria to help other Syrian physicians considering this disease in the differential diagnosis if they face similar presentations.
骨软骨瘤病是一种罕见的非遗传性骨骼疾病，其特征为多发性内生软骨瘤，即软骨的非癌性生长。在本报告中，我们介绍了一名10岁叙利亚男孩患骨软骨瘤病的病例。该患者手部出现多个骨肿块；他5岁时曾有过病理性骨折史，导致肢体残疾。我们分析了该患者的临床、影像学和病理特征，这有助于我们做出最终诊断。骨软骨瘤病是一种良性骨肿瘤，但有恶变为软骨肉瘤的风险。本报告的目的是记录叙利亚存在骨软骨瘤病，以帮助其他叙利亚医生在遇到类似病例时，在鉴别诊断中考虑这种疾病。
