Friedmann I, Galey F R
J Laryngol Otol. 1980 Nov;94(11):1215-29. doi: 10.1017/s0022215100090046.
The ultrastructure of tympanosclerotic tissue is described with particular reference to the structure of matrix vesicles and calcospherules, often of intricate structure, and to their role in the induction of calcification. The vesicles formed by degenerating cells within the collagenous matrix or epithelium of the tympanosclerotic tissues are the primary site of calcification. The released spherules appear scattered throughout the collagenous layers, and form the organic basis of calcospherules. Through fusion larger aggregates are formed which lead to the development of macroscopically recognizable calcified plaques in the middle ear cleft. The entire process is triggered off by the inflammatory processes of otitis media. Compared with other processes of excessive fibrogenesis and calcification, tympanosclerosis fits well into the overall scheme of induced calcification in both normal and pathological conditions which is similar in all mineralizing tissues composed of collagen and protoglycons. The cause of the prolific fibrogenesis and mineralization has remained doubtful. Clearly inflammatory and degenerative processes in otitis media may trigger off the release of a factor (or factors), and of matrix vesicles acting as fibrogenetic stimulants and primary sites of calcification. Katchburian's working hypothesis of mineralization (Katchburian, 1973) has universal appeal and can be confirmed on the basis of our observations on tympanosclerosis. Tympanosclerosis may be added to the 'crystal deposition diseases' of McCarthy.
本文描述了鼓室硬化组织的超微结构,特别提及基质小泡和钙球的结构,它们通常具有复杂的结构,以及它们在钙化诱导中的作用。鼓室硬化组织的胶原基质或上皮内退变细胞形成的小泡是钙化的主要部位。释放出的球状体散在于胶原层中,构成钙球的有机基础。通过融合形成更大的聚集体,导致中耳裂中出现宏观上可识别的钙化斑块。整个过程由中耳炎的炎症过程引发。与其他过度纤维生成和钙化过程相比,鼓室硬化很好地符合了正常和病理条件下诱导钙化的总体模式,这在所有由胶原和蛋白聚糖组成的矿化组织中都是相似的。纤维生成和矿化过多的原因仍不明确。显然,中耳炎中的炎症和退变过程可能引发一种(或多种)因子的释放,以及作为纤维生成刺激物和钙化主要部位的基质小泡的释放。卡奇布里安的矿化工作假说(卡奇布里安,1973年)具有普遍的吸引力,并且可以根据我们对鼓室硬化的观察得到证实。鼓室硬化可被添加到麦卡锡的“晶体沉积疾病”中。