Karosi Tamás, Kónya József, Petkó Mihály, Sziklai István
Departments of Otolaryngology Head & Neck Surgery, University Medical School of Debrecen, Debrecen, Hungary.
Otol Neurotol. 2005 Nov;26(6):1128-33. doi: 10.1097/01.mao.0000169304.72519.d2.
Persistent measles virus infection of the otic capsule is presumed to be one of the etiologic factors in otosclerosis. The viral pathogenesis of otosclerosis could be established only by correlative analysis: histologic examination of the stapes footplates and reverse-transcriptase polymerase chain reaction amplification of the viral RNA. At present, histologic analysis of the removed stapes footplates is the only appropriate method of distinguishing otosclerotic and nonotosclerotic stapes fixations.
The presence of measles virus was shown in otosclerotic patients by reverse-transcriptase polymerase chain reaction amplification of the viral RNA and detecting the viral proteins by immunohistochemistry.
Nucleic acids (mRNA, vRNA, and DNA) were extracted from ankylotic stapes footplates of stapes fixation patients (n = 44). Measles virus genomic nucleoprotein RNA was amplified by seminested reverse-transcriptase polymerase chain reaction. Amplification results were correlated to postoperative histologic findings.
Measles virus RNA was detectable only in histologically otosclerotic stapes footplates (n = 32). Histology for virus-negative footplates (n = 12) excluded otosclerosis. Virus-negative stapes footplates showed annular calcification (n = 8), bone resorption with increased numbers of hemosiderophages (n = 2), and mononuclear cell infiltration with osteolysis (n = 2).
Stapes ankylosis is a heterogenous disease causing conductive hearing loss with different causes. Nonotosclerotic stapes fixations may belong to degenerative disorders with variable histopathology. Otosclerosis is an inflammatory disease resulting from persisting measles virus infection of the otic capsule.
镫骨足板的持续性麻疹病毒感染被认为是耳硬化症的病因之一。耳硬化症的病毒发病机制只能通过相关分析来确定:镫骨足板的组织学检查以及病毒RNA的逆转录酶聚合酶链反应扩增。目前,对切除的镫骨足板进行组织学分析是区分耳硬化性和非耳硬化性镫骨固定的唯一合适方法。
通过病毒RNA的逆转录酶聚合酶链反应扩增以及免疫组织化学检测病毒蛋白,在耳硬化症患者中发现了麻疹病毒的存在。
从镫骨固定患者(n = 44)的强直镫骨足板中提取核酸(mRNA、vRNA和DNA)。通过半巢式逆转录酶聚合酶链反应扩增麻疹病毒基因组核蛋白RNA。将扩增结果与术后组织学结果相关联。
仅在组织学上为耳硬化性的镫骨足板(n = 32)中可检测到麻疹病毒RNA。病毒阴性足板(n = 12)的组织学检查排除了耳硬化症。病毒阴性的镫骨足板表现为环形钙化(n = 8)、含铁血黄素巨噬细胞数量增加的骨质吸收(n = 2)以及伴有骨质溶解的单核细胞浸润(n = 2)。
镫骨强直是一种导致传导性听力损失的异质性疾病,病因各不相同。非耳硬化性镫骨固定可能属于具有不同组织病理学的退行性疾病。耳硬化症是一种由耳囊持续性麻疹病毒感染引起的炎症性疾病。