骨软骨瘤的矿化过程。扫描电镜研究]。

M Fadda, G Zirattu
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引用次数: 0

摘要

30例骨软骨瘤患者分为两组:15例处于发育期,15例已结束发育期。患者年龄4 ~ 42岁;其中18人是男性。在次氯酸盐处理标本后,研究了骨软骨组织的矿化过程。mp在患者发育过程中尤为明显,其特征是与交叉胶原纤维相关的圆形钙化结节(钙球粒)。M.P.在形态学上与通常在正常和病理标本中观察到的相似。除两例外,在发育末期,骨小梁间隙无钙化物质。在这两个病例中,我们观察到恢复的M.P.矿化是钙球型的,并从化生软骨岛开始。这被解释为可能转变为外周软骨肉瘤的迹象。在第三个病例中,破骨细胞活动引起深层、广泛的骨膜下和小梁侵蚀,导致骨软骨肿瘤组织内陷。
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[The mineralization process in osteochondroma. A scanning electron microscopic study].

Thirty patients affected by osteochondroma were divided in two groups: 15 patients were in the age of development, and 15 patients had ended their development. The patients' age ranged from 4 to 42 years; 18 of them were males. The mineralization process (M.P.) of the osteochondral tissue was studied following hypochlorite treatment of the specimens. M.P. was particularly evident in patients during development and was characterized by round calcific nodules (calcospherites) which were linked to crossed collagen fibers. M.P. was morphologically similar to what is usually observed in normal and pathological specimens. Except in two cases, at the end of development the intertrabecular spaces were free of calcific material. In those two cases we observed a resumption of M.P. Mineralization was of calcospheritic type and started from islands of metaplastic cartilage. It was interpreted as a sign of possible transformation to peripheral chondrosarcoma. In a third case, osteoclastic activity caused deep, wide subperiosteal and trabecular erosion resulting in osteocartilaginous neoplastic tissue involution.

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