Al Kaissi Ali, Ganger Rudolf, Klaushofer Klaus, Grill Franz
Ludwig Boltzmann Institute of Osteology, Hanusch Hospital of WGKK and AUVA Trauma Centre Meidling, First Medical Department Heinrich Collin Strasse 30 A, 1140 Vienna, Austria ; Paediatric Department, Orthopädisches Spital Speising, Speisinger Strasse 109 A, 1130 Vienna, Austria.
Case Rep Orthop. 2013;2013:758168. doi: 10.1155/2013/758168. Epub 2013 Nov 10.
We report on a 13-year-old boy who presented with multiple hereditary exostosis and had development of back pain, associated with neurological deficits, and was found to have exostoses in the spinal canal. Spine radiograph showed a cauliflower-like abnormality of multiple exostoses of the posterior arch (pedicle) of the thoracic vertebrae (T3-5). Reformatted CT scanning revealed the simultaneous development of intra- and extraspinal osteochondromatosis of T3-5. The spinal cord was compressed by the intraspinal exostosis. Our patient was surgically treated for intraspinal exostoses and showed cessation of neurological deficits. We report what might be a rare association of spinal cord compression in a patient with multiple hereditary exostoses.
我们报告了一名13岁男孩,他患有多发性遗传性骨软骨瘤,并出现背痛,伴有神经功能缺损,且在椎管内发现有骨软骨瘤。脊柱X线片显示胸椎(T3 - 5)后弓(椎弓根)多发性骨软骨瘤呈菜花状异常。CT重建扫描显示T3 - 5同时发生椎管内和椎管外骨软骨瘤病。脊髓被椎管内骨软骨瘤压迫。我们的患者接受了椎管内骨软骨瘤的手术治疗,神经功能缺损停止。我们报告了一例多发性遗传性骨软骨瘤患者中可能罕见的脊髓受压关联情况。