Miller Mia E, Kirsch Claudia, Canalis Rinaldo F
Division of Head and Neck Surgery, David Geffen School of Medicine at UCLA, Los Angeles, California 90095-1624, USA.
Ann Otol Rhinol Laryngol. 2010 May;119(5):319-24. doi: 10.1177/000348941011900508.
We present a familial association of radiographically and surgically demonstrated mallear fixation with concurrent stapedial abnormality and dehiscence of the facial nerve in a father and son, including history, physical findings, surgical findings, radiologic analyses, and a literature review. A 12-year-old boy presented with long-term left-sided conductive hearing loss, and was found to have mallear fixation and a dehiscent facial nerve on a computed tomographic (CT) scan of the temporal bone. Release of the malleus was performed at surgery, revealing hypermobility of the remaining ossicular chain. A repeat CT scan of the temporal bone showed successful release of the mallear head. The patient's father later presented with bilateral hearing loss, and a CT scan of the temporal bones showed bilateral osseous fixation of the mallear head to the tegmen and bilateral facial nerve dehiscences. He underwent right middle ear exploration, but release of the malleus was not performed because of the risk to the dehiscent facial nerve. The stapes crurae were found to be filiform at surgery. This is the first reported familial association of mallear fixation. Mallear fixation with facial nerve dehiscence and an abnormal stapes occurring in a parent and his child is interesting embryologically, and suggests that these anomalies may be genetically linked.
我们报告了一例父子间影像学和手术证实的锤骨固定与镫骨异常及面神经裂同时存在的家族性关联,包括病史、体格检查结果、手术发现、影像学分析及文献综述。一名12岁男孩长期左侧传导性听力损失,颞骨计算机断层扫描(CT)显示锤骨固定及面神经裂。手术中松解锤骨,发现其余听骨链活动过度。颞骨重复CT扫描显示锤骨头成功松解。该患者的父亲后来出现双侧听力损失,颞骨CT扫描显示双侧锤骨头与鼓室盖骨性固定及双侧面神经裂。他接受了右中耳探查,但因面神经裂风险未进行锤骨松解。手术中发现镫骨脚呈丝状。这是首次报道的锤骨固定家族性关联。父母及其子女中出现的锤骨固定伴面神经裂和镫骨异常在胚胎学上很有意思,提示这些异常可能存在遗传联系。