Sulica V I, Cooper P H, Pope F M, Hambrick G W, Gerson B M, McKusick V A
Arch Dermatol. 1979 Jan;115(1):40-2.
Skin biopsy specimens from 21 patients with Ehlers-Danlos syndrome (EDS) were compared with controls. With two exceptions, the appearance of the dermal collagen and elastic tissue as seen in the two groups was indistinguishable. One example of type 4 EDS contained a dermis composed of fibers that resembled actinically damaged elastic tissue. The single example of type 6 EDS contained particularly thin collagen fibers. The dermal thickness of specimens of EDS was similar to that of controls, although the abnormal-appearing specimen of type 4 EDS was also abnormally thin. Since the other two biopsy specimens of type 4 appeared to be within the range of normal, there may be heterogeneity in this form of EDS.
将21例埃勒斯-当洛综合征(EDS)患者的皮肤活检标本与对照组进行了比较。除两例外,两组中所见的真皮胶原和弹性组织外观无明显差异。1例4型EDS的真皮由类似于光化损伤弹性组织的纤维组成。1例6型EDS的胶原纤维特别细。EDS标本的真皮厚度与对照组相似,尽管4型EDS外观异常的标本也异常薄。由于4型的另外两份活检标本似乎在正常范围内,这种形式的EDS可能存在异质性。