Hwang W S, Tock E P, Tan K L, Tan L K
J Pathol. 1979 Jan;127(1):11-8. doi: 10.1002/path.1711270103.
The pathology of four types of chondrodysplasias, viz., type II achondrogenesis, thanatophoric dwarfism, Saldino-Noonan syndrome, and chondrodysplasia punctata were studied. In each of these disorders, cells with features similar to the chief and dark chondrocytes of normal hyaline cartilage were seen to be altered in different ways. There was a total absence of chief cells in type II achondrogenesis. All the chondrocytes present were of one variety at different states of maturation, with the fully matured cell having features of dark chondrocytes. The absence of chief cells was associated with marked diminution of interlacunar matrix and failure of growth plate development. The chief chondrocytes in thanatophoric dwarfism appeared diminished in number. They were probably abnormal functionally as evident by their lack of cytoplasmic vacuolation and the formation of thick, occasionally branched collagen in the matrix. The growth plate was stunted and poorly developed. Striking changes involving the dark cells were noted in Saldino-Noonan syndrome, where unusually elongated dark cells were found in groups within abnormal cystic spaces. The chief cells were large and contained abnormal cytoplasmic filaments. There was no formation of a growth plate. In chondrodysplasia punctata, the chief cells were enlarged and abnormally vacuolated. The matrix showed excessive aggregates of coarse granular material. In addition, there were focal accumulations of highly abnormal chief and dark cells with abnormal matrix which contained increased amount of keratan sulphate and culminated in spotty calcification.
对四种软骨发育异常,即II型软骨发育不全、致死性侏儒症、Saldino-Noonan综合征和点状软骨发育不良的病理学进行了研究。在这些疾病中,可见具有与正常透明软骨的主要软骨细胞和暗软骨细胞相似特征的细胞发生了不同方式的改变。II型软骨发育不全中完全没有主要细胞。所有存在的软骨细胞都是处于不同成熟状态的同一类型,完全成熟的细胞具有暗软骨细胞的特征。主要细胞的缺失与腔隙间基质的显著减少和生长板发育失败有关。致死性侏儒症中的主要软骨细胞数量似乎减少。它们在功能上可能是异常的,这从它们缺乏细胞质空泡化以及基质中形成粗大、偶尔分支的胶原可以明显看出。生长板发育迟缓且发育不良。在Saldino-Noonan综合征中发现了涉及暗细胞的显著变化,在异常的囊性空间内成组地发现了异常细长的暗细胞。主要细胞很大,含有异常的细胞质细丝。没有形成生长板。在点状软骨发育不良中,主要细胞增大且异常空泡化。基质显示出粗大颗粒物质的过度聚集。此外,存在高度异常的主要软骨细胞和暗细胞的局灶性聚集以及异常基质,该基质含有增加量的硫酸角质素并最终导致斑点状钙化。