Department of Physical Therapy and Rehabilitation, Faculty of Medicine, Adnan Menderes University, Aydin, Turkey.
Rheumatol Int. 2010 Mar;30(5):699-703. doi: 10.1007/s00296-009-0983-7. Epub 2009 Jun 6.
Ollier disease is a rare, non-hereditary mesodermal dysphasia, characterized by multiple enchondromas, which demonstrate asymmetric involvement of the metaphyses of the long bones. Many malignancies, especially chondrosarcomas, may be observed in association with this disease. The clinical and radiologic characteristics of a case involving a 44-year-old male patient with non-small cell lung cancer are presented together with the clinical characteristics of other cases reported in the literature.
奥利耶病是一种罕见的非遗传性中胚层发育不良，其特征为多发性内生软骨瘤，表现为长骨干骺端的不对称性受累。许多恶性肿瘤，特别是软骨肉瘤，可能与此病相关。本文报告了 1 例 44 岁男性非小细胞肺癌患者的临床和影像学特征，并结合文献中报道的其他病例的临床特征进行了讨论。
