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迪格维-梅尔基奥尔-克劳森综合征。生长板的组织化学研究。

Dyggve-Melchior-Clausen syndrome. A histochemical study of the growth plate.

作者信息

Horton W A, Scott C I

出版信息

J Bone Joint Surg Am. 1982 Mar;64(3):408-15.

PMID:6277958
Abstract

UNLABELLED

The Dyggve-Melchior-Clausen syndrome is a rare inherited disorder in which a major feature, the skeletal dysplasia, is thought to result from a defect in endochondral ossification. To further characterize this disturbance, histochemical studies were performed on an iliac-crest biopsy specimen from a patient with disorder. The use of plastic embedding methods permitted previous observations, which were based on decalcified paraffin-embedded tissues, to be extended and a variety of new ones to be made. The resting cartilage matrix was very fibrous. In many areas it consisted of randomly oriented bundles of loosely woven fibers that stained as collagen. The chondrocytes in this region were excessively vacuolated and many contained cytoplasmic inclusions that stained non-specifically as protein. Cartilage canals were prominent in the resting cartilage. In many areas, clusters of degenerating chondrocytes and occasional vacuolar lesions replaced the columns of proliferating and maturing cells that normally occupy the growth-plate region. There was coarse and irregular calcification of these clusters at the chondro-osseous junction, and intracartilaginous ossification was also found.

CLINICAL RELEVANCE

These observations further define the histological criteria for the diagnosis of this disorder and provide new insights into its pathogenesis.

摘要

未标注

戴格维-梅尔基奥尔-克劳森综合征是一种罕见的遗传性疾病,其主要特征骨骼发育异常被认为是由于软骨内骨化缺陷所致。为了进一步明确这种紊乱情况,对一名患有该疾病患者的髂嵴活检标本进行了组织化学研究。使用塑料包埋方法使基于脱钙石蜡包埋组织的先前观察得以扩展,并得出了各种新的观察结果。静止软骨基质非常纤维化。在许多区域,它由随机排列的松散编织纤维束组成,这些纤维束染色显示为胶原蛋白。该区域的软骨细胞过度空泡化,许多细胞含有细胞质内含物,这些内含物染色显示为非特异性蛋白质。软骨管在静止软骨中很突出。在许多区域,退化软骨细胞簇和偶尔的空泡性病变取代了正常占据生长板区域的增殖和成熟细胞柱。在软骨-骨交界处,这些簇有粗大且不规则的钙化,并且还发现了软骨内骨化。

临床意义

这些观察结果进一步明确了该疾病诊断的组织学标准,并为其发病机制提供了新的见解。

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