Trüeb R M, Tsambaos D, Spycher M A, Müller J, Burg G
Department of Dermatology, University Hospital of Zurich, Switzerland.
Dermatology. 1997;194(2):191-4. doi: 10.1159/000246097.
Several clinical syndromes are characterized by ectodermal dysplasia (ED) in association with clefting of the lip and/or palate. In these syndromes, alopecia is primarily due to abnormalities of the hair shaft associated with increased hair fragility. Scalp dermatitis is yet another peculiar finding, primarily seen in the ankyloblepharon-ED-clefting (AEC) syndrome. We report on a 16-year-old patient with ectrodactyly-ED-clefting (EEC) syndrome, who exhibited a scarring alopecia due to deep folliculitis. On scanning electron microscopy, irregular torsion and longitudinal grooving of the hair shaft (pili torti et canaliculi) were observed. Quantitative determinations of the elastic and viscous parameters of hair demonstrated a normal viscosity but a significantly reduced hair elasticity, indicating either an abnormal composition or a disordered arrangement of microfibrils within the apparently normal keratin matrix. In contrast to the erosive scalp dermatitis of early onset in the AEC syndrome, alopecia in this case of EEC syndrome demonstrated follicular scarring with onset during puberty. We question a possible role of the anatomical hair abnormality in the pathogenesis of chronic deep folliculitis in this and clinically related syndromes.
几种临床综合征的特征是外胚层发育不良(ED)合并唇裂和/或腭裂。在这些综合征中,脱发主要是由于毛干异常导致头发脆性增加。头皮皮炎是另一个独特的发现,主要见于睑 ankyloblepharon-ED-腭裂(AEC)综合征。我们报告了一名16岁患有缺指-外胚层发育不良-腭裂(EEC)综合征的患者,该患者因深部毛囊炎出现瘢痕性脱发。扫描电子显微镜观察发现毛干有不规则扭转和纵向沟纹(扭曲发和管腔)。对头发弹性和粘性参数的定量测定显示粘度正常,但头发弹性显著降低,表明在看似正常的角蛋白基质内微原纤维的组成异常或排列紊乱。与AEC综合征早期发作的糜烂性头皮皮炎不同,该例EEC综合征的脱发表现为青春期开始的毛囊瘢痕形成。我们质疑这种解剖学上头发异常在该综合征及临床相关综合征慢性深部毛囊炎发病机制中可能起的作用。