Ulualp Seckin O, Wright Charles G, Pawlowski Karen, Roland Peter S
Department of Otolaryngology-Head and Neck Surgery, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9035, U.S.A.
Laryngoscope. 2004 Dec;114(12):2239-42. doi: 10.1097/01.mlg.0000149465.80703.8e.
To describe pathologic findings from temporal bones acquired from an infant with Leigh disease.
Retrospective case review.
Temporal bones were taken at autopsy from an 8-month-old infant with Leigh disease. The right temporal bone was studied by microdissection. The middle ear was examined and the inner ear sensory organs dissected for study by light microscopy. The left temporal bone was embedded in celloidin, and sections were cut for microscopic examination.
Middle ear structures were normal bilaterally. There was, however, evidence of otitis media in both middle ears, which was more severe on the left side. Inner and outer hair cell loss, patchy degeneration of organ of Corti, and loss of nerve fibers in the osseous spiral lamina were found in the basal and middle turns of both cochleas. Basophilic deposits in the stria vascularis were observed in the apical portion of the left cochlea.
Inner ear sensorineural degeneration may occur in Leigh disease. Possible cochlear dysfunction caused by the degenerative changes needs to be considered in the hearing assessment of patients with Leigh disease.
描述从患有 Leigh 病的婴儿获取的颞骨的病理发现。
回顾性病例分析。
对一名患有 Leigh 病的 8 个月大婴儿进行尸检时获取颞骨。对右侧颞骨进行显微解剖研究。检查中耳,并解剖内耳感觉器官以进行光学显微镜检查。将左侧颞骨包埋在火棉胶中,切片进行显微镜检查。
双侧中耳结构正常。然而,双侧中耳均有中耳炎迹象,左侧更为严重。在双侧耳蜗的基部和中部发现内、外毛细胞丢失、柯蒂氏器斑片状变性以及骨螺旋板神经纤维丢失。在左侧耳蜗顶部观察到血管纹中的嗜碱性沉积物。
Leigh 病可能会发生内耳感觉神经性退变。在对 Leigh 病患者进行听力评估时,需要考虑由这些退行性变化引起的可能的耳蜗功能障碍。