Shapiro F
Department of Orthopaedic Surgery, Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115.
Calcif Tissue Int. 1992 Oct;51(4):324-31. doi: 10.1007/BF00334495.
Light and electron microscopic studies of diastrophic dysplasia iliac crest growth cartilage performed on five occasions in two patients from 1 to 10 years of age reveal extensive cell and matrix abnormalities at each time period. Light microscopy shows atypical chondrocytes with extreme variation in size and shape, and premature cytoplasmic degeneration, and formation of target ghost cells. Prominent, densely staining fibrotic foci are present throughout the cartilage. Ultrastructure reveals some structurally intact chondrocytes with a single large fat inclusion, slightly dilated rough endoplasmic reticulum, and abundant glycogen. As early as 1 year of age cystic degeneration of chondrocyte cytoplasm is evident with indistinct organelles seen. The cartilage matrix demonstrates a general increase in fibrous tissue as well as the fibrotic foci. The collagen in these foci is remarkably abnormal. It is composed of short, extremely broad fibrils ranging from 150 to 950 nm in width which are separated at their terminal ends but fused to each other centrally in random fashion. On cross-section there are very few round fibrils but rather a marked irregularity in shape giving the appearance of having fibrils randomly added to others to form enlarged nonuniform fibril aggregates. On longitudinal sectioning, regular cross-banding across the entire fibril width is seen but fibril splitting and aggregation are highly irregular.(ABSTRACT TRUNCATED AT 250 WORDS)
对两名1至10岁患者的脊柱发育不良性髂嵴生长软骨进行了五次光镜和电镜研究,结果显示在每个时间段均存在广泛的细胞和基质异常。光镜下可见非典型软骨细胞,其大小和形状差异极大,细胞质过早变性,并形成靶形鬼影细胞。整个软骨中可见突出的、染色致密的纤维化灶。超微结构显示一些结构完整的软骨细胞,有单个大的脂肪包涵体、轻度扩张的粗面内质网和丰富的糖原。早在1岁时,软骨细胞胞质的囊性变性就很明显,细胞器模糊不清。软骨基质显示纤维组织普遍增加以及纤维化灶。这些病灶中的胶原明显异常。它由宽度为150至950纳米的短而极宽的纤维组成,这些纤维在末端分开,但在中央以随机方式相互融合。在横切面上,圆形纤维很少,而是形状明显不规则,看起来像是纤维随机添加到其他纤维上形成扩大的不均匀纤维聚集体。在纵切面上,可见整个纤维宽度上有规则的交叉带,但纤维分裂和聚集非常不规则。(摘要截短于250字)