Alpizar-Aguirre Armando, Elías-Escobedo Alejandro, Rosales-Olivares Luis M, Miramontes-Martínez Víctor, Reyes-Sánchez Alejandro
Instituto Nacional de Rehabilitación (INR), Secretaría de Salud, México, D. F.
Cir Cir. 2008 May-Jun;76(3):205-11.
Vertebral Destruction Syndrome (VDS) is a pathology of multiple etiologies causing structural alterations of the spine, producing deformity with neurological and mechanical alterations. In order to study VDS, a diagnostic process is carried out, sometimes with unexpected results. We undertook this study to validate the systematization of a series of studies to arrive at the diagnosis of VDS.
We included 105 patients in the study with diagnosis of VDS from January 1998 to December 2005, taking into consideration specificity, sensitivity and predictive value of each integrated study in order to determine its diagnostic value.
The most frequent etiology was Pott's Disease (24 cases) followed by osteomyelitis (20 cases), metastasis (18 cases) and multiple myeloma and plasmacytoma (16 cases each). The higher sensitivity in Pott's Disease was obtained with bone scan and polymerase chain reaction (PCR); for multiple myeloma, computerized axial tomography (CAT) and bone scan; CAT and bone scan for infections; MRI for primary tumors; and MRI and bone scan for secondary tumors.
To reduce false positives to 2% and to reduce the maximum number of false negatives, studies such as CAT, MRI, bone scan, PCR, ESR, C-reactive protein and determination of alkaline and acid phosphatase must be included in the VDS study protocol. Other studies have very low diagnostic sensitivity and specificity.
椎体破坏综合征(VDS)是一种由多种病因引起的病理状态,可导致脊柱结构改变,产生伴有神经和机械改变的畸形。为了研究VDS,需进行诊断过程,有时会得到意想不到的结果。我们开展这项研究以验证一系列研究的系统化,从而得出VDS的诊断。
我们纳入了1998年1月至2005年12月期间诊断为VDS的105例患者,考虑每项综合研究的特异性、敏感性和预测价值,以确定其诊断价值。
最常见的病因是脊柱结核(24例),其次是骨髓炎(20例)、转移瘤(18例)以及多发性骨髓瘤和浆细胞瘤(各16例)。骨扫描和聚合酶链反应(PCR)对脊柱结核具有较高的敏感性;计算机断层扫描(CAT)和骨扫描对多发性骨髓瘤具有较高的敏感性;CAT和骨扫描对感染具有较高的敏感性;MRI对原发性肿瘤具有较高的敏感性;MRI和骨扫描对继发性肿瘤具有较高的敏感性。
为了将假阳性率降低至2%并减少假阴性的最大数量,VDS研究方案必须包括CAT、MRI、骨扫描、PCR、血沉、C反应蛋白以及碱性和酸性磷酸酶测定等检查。其他检查的诊断敏感性和特异性非常低。