Sørensen Mads Sølvsten, Frisch Thomas, Bretlau Poul
Otopathological Laboratory, Department of Otolaryngology Head and Neck Surgery, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Adv Otorhinolaryngol. 2007;65:53-58. doi: 10.1159/000098670.
The pathological perilabyrinthine bone remodelling of otosclerosis is associated with a genetic predisposition and triggered by mechanisms so far unknown. A proposed viral aetiology of otosclerosis originates from a similar concept of Paget's disease. However, at present, it is not clear why a virus should cause otosclerosis, confined to the bony otic capsule with no effects on the general skeleton in some patients, and systemic Paget's disease with only occasional involvement of the bony otic capsule in others. Moreover, the extent and distribution of pathological bone remodelling is different in Paget's disease of the temporal bone and in otosclerosis. Bone resorption and consequently bone remodelling which turns over the general skeleton at a rate of 10% per year is normally highly restricted in perilabyrinthine bone to a minimum of 0.13% per year except in otosclerosis, and systemic remodelling rates are normal even in otosclerotic patients. This suggests the existence of a local inner ear mechanism in control of capsular remodelling activity, which is either overruled, bypassed or most likely defective in otosclerosis, no matter what may have triggered the disease process. We present experimental data related to this mechanism, which may offer a truly local pathogenetic factor in otosclerosis.
耳硬化症的病理迷路周围骨重塑与遗传易感性相关,其触发机制至今不明。一种关于耳硬化症的病毒病因学假说源于与佩吉特病类似的概念。然而,目前尚不清楚为何病毒会导致耳硬化症,在一些患者中局限于骨迷路包囊而对全身骨骼无影响,而在另一些患者中则导致全身性佩吉特病,仅偶尔累及骨迷路包囊。此外,颞骨佩吉特病和耳硬化症中病理性骨重塑的程度和分布有所不同。正常情况下,除耳硬化症外,迷路周围骨的骨吸收以及由此导致的每年以10%的速率更新全身骨骼的骨重塑通常受到高度限制,每年最低为0.13%,即使是耳硬化症患者,全身的重塑速率也是正常的。这表明存在一种局部内耳机制来控制包囊重塑活动,在耳硬化症中,无论引发疾病过程的原因是什么,这种机制要么被推翻、绕过,要么很可能存在缺陷。我们展示了与该机制相关的实验数据,这可能为耳硬化症提供一个真正的局部致病因素。