Pierard G E, Pierard-Franchimont C, Lapière C M
Int J Dermatol. 1983 Jun;22(5):300-4. doi: 10.1111/j.1365-4362.1983.tb02142.x.
The Ehlers-Danlos syndrome is commonly divided into at least 8 types according to clinical, genetic, and biochemical aspects. We propose histological criteria that would permit a more precise diagnosis of the gravis and mitis types. In the gravis type, collagen bundles are thin and rare in the dermis and hypodermal septae; in polarized light, they are less refringent than in normal skin. This is associated with an increase in the relative proportion of elastic fibers. In the mitis type, the looseness of the collagen network is much less evident; elastic fibers are not in excess but irregular in size, shape, distribution, and orientation.
埃勒斯-当洛综合征通常根据临床、遗传和生化方面至少分为8种类型。我们提出了组织学标准,以更精确地诊断重症型和轻症型。在重症型中,真皮和皮下间隔中的胶原束细且稀少;在偏振光下,它们的折光性比正常皮肤弱。这与弹性纤维相对比例的增加有关。在轻症型中,胶原网络的疏松程度不太明显;弹性纤维不过多,但大小、形状、分布和方向不规则。