INSERM U930/CNRS ERL 3106, Université François Rabelais, Tours, France.
Am J Clin Dermatol. 2010;11(4):269-73. doi: 10.2165/11530090-000000000-00000.
Ehlers-Danlos syndrome (EDS) is a heterogenous group of diseases that can be potentially life threatening in the vascular form. The diagnosis is mainly based on a clinical score including many items that demonstrate skin, mucosa, joint, and vessel involvement. The score is particularly helpful in hypermobile and classical forms but can be normal in the vascular type. The absence of the lingual and inferior labial frenula was reported to be a useful diagnostic tool in a series of 12 patients with classical and hypermobile EDS. However, two further reports have contested the value of this sign.
To determine the diagnostic value of the absence of inferior labial or lingual frenula in EDS.
Patients with EDS were prospectively recruited from November 2006 to April 2007 in a French tertiary center. Each patient was examined to check for the presence or absence of the oral frenula and matched with two controls seen from February to May 2007.
Forty-three patients (ratio female/male of 2.07 : 1, mean age 31 years, range 4-63 years), 4 with classical EDS, 19 with hypermobile EDS, and 20 with vascular-type EDS, were included and matched with 86 controls. The sensitivity of the absence of the inferior labial frenulum was 42% (95% CI 27, 58) and for the lingual frenulum was 53.5% (95% CI 38, 69). The specificity was 99% (95% CI 94, 100) and 98% (95% CI 92, 100), respectively. In the vascular group, 13 of 20 patients were affected (sensitivity = 65% [95% CI 41, 85]; specificity = 97% [95% CI 87, 100]; odds ratio = 72 [95% CI 8, 645]). Inter-observer agreement was excellent (kappa value 0.91).
The absence of the inferior labial frenulum or lingual frenulum is a specific sign of EDS that can be easily checked by a physician. It can be helpful in the early diagnosis of the disease, including the vascular type, in affected families. It can also be helpful to distinguish between joint hypermobility syndrome and the hypermobile type of EDS in patients with joint hypermobility.
埃勒斯-当洛斯综合征(EDS)是一组异质性疾病,在血管型中可能具有潜在的生命威胁。该诊断主要基于包括皮肤、黏膜、关节和血管受累在内的多项表现的临床评分。该评分在高活动型和经典型中特别有用,但在血管型中可能正常。在一系列 12 例经典和高活动型 EDS 患者中,报道舌系带和下唇系带缺失是一种有用的诊断工具。然而,另外两项报告对该体征的价值提出了质疑。
确定下唇系带或舌系带缺失在 EDS 中的诊断价值。
2006 年 11 月至 2007 年 4 月,在法国的一个三级中心前瞻性招募 EDS 患者。对每位患者进行检查,以确定口腔系带的存在或缺失,并与 2007 年 2 月至 5 月期间的 86 名对照组相匹配。
43 例患者(女性/男性比例为 2.07:1,平均年龄 31 岁,范围 4-63 岁),4 例为经典 EDS,19 例为高活动型 EDS,20 例为血管型 EDS,与 86 名对照组相匹配。下唇系带缺失的敏感性为 42%(95%CI 27, 58),舌系带缺失的敏感性为 53.5%(95%CI 38, 69)。特异性分别为 99%(95%CI 94, 100)和 98%(95%CI 92, 100)。在血管组中,20 例患者中有 13 例受影响(敏感性=65%[95%CI 41, 85];特异性=97%[95%CI 87, 100];优势比=72[95%CI 8, 645])。观察者间一致性极好(kappa 值 0.91)。
下唇系带或舌系带缺失是 EDS 的一种特异性体征,医生可以通过它进行简单的检查。它有助于在疾病早期诊断,包括受累家族中的血管型,也有助于在关节活动过度的患者中区分关节过度活动综合征和 EDS 的高活动型。