Wolfowitz B
Arch Otolaryngol. 1979 Aug;105(8):496-9. doi: 10.1001/archotol.1979.00790200058012.
Unilateral congenital sensorineural deafness was observed in a 4-year-old boy. The patient had fluid in the left tympanic cavity, simulating serous otitis, which was caused by a spontaneous CSF leak from the oval window, around the edges of a normal stapedial footplate. Polytomography demonstrated an inner ear dysplasia, viz, dilation of the lateral semicircular canal, vestibule, and cochlea. The CSF leak was controlled by packing the vestibule with muscle and fascia. The literature related to this rare syndrome is reviewed.
一名4岁男孩被发现患有单侧先天性感音神经性耳聋。该患者左侧鼓室内有积液,类似浆液性中耳炎,这是由卵圆窗处自发性脑脊液漏引起的,漏口位于正常镫骨足板边缘周围。体层摄影术显示内耳发育异常,即外侧半规管、前庭和耳蜗扩张。通过用肌肉和筋膜填充前庭来控制脑脊液漏。本文回顾了与这种罕见综合征相关的文献。