Sone M, Schachern P A, Paparella M M, Morizono N
Otitis Media Research Center, Department of Otolaryngology, University of Minnesota School of Medicine, Minneapolis, USA.
Ann Otol Rhinol Laryngol. 1999 Apr;108(4):338-44. doi: 10.1177/000348949910800404.
Despite some reports of sensorineural hearing loss with systemic lupus erythematosus (SLE), its pathologic correlate has remained unidentified due to the scarcity of human temporal bone studies. We here present findings in 14 temporal bones from 7 patients with SLE, examined histologically and immunohistochemically for pathologic conditions in the cochlea that might relate to their otologic histories. Blue-staining concretions were seen in the stria vascularis of 6 ears. Most of the cases showed a loss of spiral ganglion cells, with various degrees of hair cell loss and atrophy of the stria vascularis. One ear demonstrated formation of fibrous tissue and bone throughout the cochlea, with complete loss of the membranous labyrinth. Cochlear hydrops was found in only 1 ear. These findings in temporal bones from patients with SLE are discussed in relation to autoimmune disease of the inner ear.
尽管有一些关于系统性红斑狼疮(SLE)伴发感音神经性听力损失的报道,但由于人类颞骨研究稀缺,其病理关联仍未明确。我们在此展示了7例SLE患者14块颞骨的研究结果,通过组织学和免疫组化检查了耳蜗中可能与其耳科病史相关的病理状况。在6只耳朵的血管纹中可见蓝色染色的结石。大多数病例显示螺旋神经节细胞缺失,伴有不同程度的毛细胞缺失和血管纹萎缩。一只耳朵在整个耳蜗中出现纤维组织和骨形成,膜迷路完全消失。仅在1只耳朵中发现耳蜗积水。本文结合内耳自身免疫性疾病对SLE患者颞骨的这些发现进行了讨论。