Kobayasi T, Oguchi M, Asboe-Hansen G
Clin Genet. 1984 Jun;25(6):477-84. doi: 10.1111/j.1399-0004.1984.tb00490.x.
Skin biopsies from thirteen patients suffering from Ehlers-Danlos syndrome, including 6 of the mitis type, 4 of the benign hypermobile type, one of the X-linked type, one of the ocular type and one of the periodontitis type, were studied by electron microscopy after routine preparation. Collagen fibrils showed a distorted arrangement of bent, curled or twisted fibrils and thread-like material. Similar changes may be seen in the skin of other hereditary disorders of connective tissue. However, abnormal collagen fibrils in normal skin suggests one of eight types of Ehlers-Danlos syndrome. Clinical variants cannot be differentiated on the basis of ultrastructural findings. Elastic fibres were normal without degenerative changes. Perineurium was lacking in dermal nerves of most patients. Fibroblast-like cells showed no cystic cisterna of endoplasmic reticula.
对13例患有埃勒斯-当洛综合征的患者进行了皮肤活检,其中包括6例轻型、4例良性活动过度型、1例X连锁型、1例眼型和1例牙周炎型。常规制备后,通过电子显微镜对这些活检样本进行了研究。胶原纤维呈现出弯曲、卷曲或扭曲的纤维以及丝状物质的扭曲排列。在其他遗传性结缔组织疾病的皮肤中也可能观察到类似变化。然而,正常皮肤中出现异常胶原纤维提示为八型埃勒斯-当洛综合征之一。临床变异型无法根据超微结构发现进行区分。弹性纤维正常,无退行性改变。大多数患者的真皮神经中缺乏神经束膜。成纤维细胞样细胞未显示内质网的囊性池。