Thanatophoric dysplasia. A report of three cases.

L Sundkvist
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Abstract

Thanatophoric dysplasia is an osteochondrodysplasia always lethal already in the neonatal period. Three cases, showing the characteristic X-ray picture of the disease, are described. Histopathologically, an abnormality in the endochondral ossification process was observed. In sections from tubular bones the growth zone was found to be irregular with deficient chondrocyte maturation, absence of orderly chondrocyte columns, and the development of coarse bone trabeculae. Moreover, prominent subperiostal bone formation could be demonstrated. A constant finding was also a fibrous band, continuous with the periosteum/perichondrium, and extending into the growth zone. From this fibrous tissue membranous bone formation, directed towards the metaphysis and appearing to add to bone length, was observed. It seems as if direct bone formation predominates in thanatophoric dysplasia.

Thanatophoric发育不良。三个病例的报告。
骨骺发育不良是一种骨软骨发育不良,在新生儿期就已具有致命性。本文描述了三例显示本病特征性x线图像的病例。组织病理学观察发现软骨内成骨过程异常。在管状骨切片中,发现生长带不规则,软骨细胞成熟不足,缺乏有序的软骨细胞柱,骨小梁发育粗糙。此外,可以证明明显的骨膜下骨形成。常见纤维带,与骨膜/软骨膜连续,并延伸至生长带。从这个纤维组织膜骨形成,直接向干骺端和似乎增加骨长度,被观察到。似乎直接骨形成在嗜盐性发育不良中占主导地位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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