Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Inserm U970, Université Paris Descartes, Paris, France.
Virchows Arch. 2012 Jun;460(6):637-49. doi: 10.1007/s00428-012-1233-z. Epub 2012 May 2.
Vascular Ehlers-Danlos syndrome (vEDS) results from a mutation in the gene encoding alpha-1, type III pro-collagen (COL3A1) and confers fragility to skin, ligament and vascular tissue. We tested the value of skin biopsy for diagnosis of vEDS through an ultrastructure scoring procedure. Study design was a multicentric, case-control, blinded trial consisting of two phases: phase 1 was to identify an ultra-structure score providing the best discriminative value for vEDS and phase 2 was to replicate this result in a different population. We enrolled 103 patients, 66 cases defined through the revised nosology for Ehlers-Danlos syndromes and 37 control subjects selected from patients referred for other pathologies. Ultrastructure of extracellular matrix was read by three to five experienced pathologists blinded for diagnosis. We used the receiver operating curves and logistic regression analysis for ranking ultrastructure scores. We created a detailed description of lesions observed in vEDS patients with 27 items (coded 0 or 1). In the phase 1 (17 cases and 20 controls), abnormal fibroblast shape, presence of lysosomes in the fibroblast and abnormal basal lamina were found to be independent discriminative items. Addition of these three items (defining an ultrastructure score) had the best diagnosis value (area under the curve (AUC) = 0.96). In the phase 2 (49 cases, 17 controls), ultrastructure score provided odds ratio of 9.76 (95 % CI 2.91-32.78), and AUC of 0.90. The ultrastructure score of skin biopsy has predictive value for the diagnosis of vEDS. Presence of two or more signs (either abnormal fibroblast, presence of lysosomes in the fibroblast or abnormal basal lamina) is very evocative of vEDS.
血管型埃勒斯-当洛斯综合征(vEDS)是由于编码α-1 型 III 型前胶原(COL3A1)的基因突变引起的,使皮肤、韧带和血管组织变得脆弱。我们通过超微结构评分程序测试了皮肤活检在 vEDS 诊断中的价值。研究设计为多中心、病例对照、盲法试验,包括两个阶段:第一阶段是确定提供 vEDS 最佳鉴别价值的超微结构评分,第二阶段是在不同人群中复制该结果。我们纳入了 103 名患者,其中 66 例为修订后的埃勒斯-当洛斯综合征分类法定义的病例,37 例为其他病理患者中选择的对照。三位至五位经验丰富的病理学家对细胞外基质的超微结构进行了盲法阅读。我们使用接收者操作曲线和逻辑回归分析对超微结构评分进行排序。我们创建了一个详细描述 vEDS 患者观察到的病变的描述,共有 27 个项目(编码为 0 或 1)。在第一阶段(17 例病例和 20 例对照)中,异常成纤维细胞形状、成纤维细胞中溶酶体的存在和异常基底膜被发现是独立的鉴别项目。添加这三个项目(定义超微结构评分)具有最佳诊断价值(曲线下面积(AUC)=0.96)。在第二阶段(49 例病例,17 例对照)中,超微结构评分提供的比值比为 9.76(95%CI 2.91-32.78),AUC 为 0.90。皮肤活检的超微结构评分对 vEDS 的诊断具有预测价值。存在两个或更多征象(异常成纤维细胞、成纤维细胞中溶酶体的存在或异常基底膜)非常提示 vEDS。