Vogel A, Schnyder U W, Stutz S B
Hautarzt. 1985 May;36(5):269-73.
Five patients with recessive pseudoxanthoma elasticum (PXE-R) and four with dominant transmission of the disease (PXE-D) belonging to the same family were studied by light and electron microscopy. In PXE-R, calcification in the elastic fibres causes their enlargement, excavation and fragmentation. On the other hand, in PXE-D irregularly shaped and unevenly lined elastic strands may form an anastomotic wickerwork intimately intermingled with the collagenous texture. In other places, elastic bundles seem to be composed of very tiny elements. Both aspects represent a dysplasia of the elastic tissue. Independently of the mode of inheritance, a variable proportion of enlarged collagen fibrils exhibit a "flower-like" structure. Additionally, in PXE-D alone a peculiar aggregation of small and large collagen fibrils is observed. Granulofilamentous material mixed with tiny collagen fibrils is found in both groups of patients. On the basis of our observations, PXE-R and PXE-D may be identified by light and electron microscopy.
对同一家族中5例隐性弹性假黄瘤(PXE-R)患者和4例显性遗传该疾病(PXE-D)的患者进行了光镜和电镜研究。在PXE-R中,弹性纤维的钙化导致其增大、凹陷和断裂。另一方面,在PXE-D中,形状不规则且排列不均匀的弹性条索可形成紧密交织在胶原质地中的吻合状柳条编织物。在其他部位,弹性束似乎由非常微小的成分组成。这两个方面均代表弹性组织发育异常。无论遗传方式如何,可变比例的增大胶原纤维呈现“花状”结构。此外,仅在PXE-D中观察到大小胶原纤维的特殊聚集。两组患者均发现有与微小胶原纤维混合的颗粒丝状物质。根据我们的观察,PXE-R和PXE-D可通过光镜和电镜进行鉴别。