Ishai Reuven, Seyyedi Mohammad, Chancellor Andrew M, McLean Catriona A, Rodriguez Michael L, Halmagyi Gabor Michael, Nadol Joseph B, Szmulewicz David J, Quesnel Alicia M
Otopathology Laboratory, Department of Otolaryngology-Head and Neck Surgery, Massachusetts Eye and Ear.
Department of Otolaryngology-Head and Neck Surgery, Harvard Medical School, Boston, Massachusetts, USA.
Otol Neurotol. 2021 Mar 1;42(3):e332-e340. doi: 10.1097/MAO.0000000000002985.
To describe the site of lesion responsible for the severe, bilateral, symmetrical, selective loss of vestibular function in Cerebellar Ataxia with Neuronopathy and Vestibular Areflexia Syndrome (CANVAS), an adult-onset recessively-inherited ataxia, characterized by progressive imbalance due to a combination of cerebellar, somatosensory, and selective vestibular impairment with normal hearing.
Histologic examination of five temporal bones and the brainstems from four CANVAS patients and the brainstem only from one more, each diagnosed and followed from diagnosis to death by one of the clinician authors.
All five temporal bones showed severe loss of vestibular ganglion cells (cell counts 3-16% of normal), and atrophy of the vestibular nerves, whereas vestibular receptor hair cells and the vestibular nuclei were preserved. In contrast, auditory receptor hair cells, the auditory ganglia (cell counts 51-100% of normal), and the auditory nerves were relatively preserved. In addition, the cranial sensory ganglia (geniculate and trigeminal), present in two temporal bones, also showed severe degeneration.
In CANVAS there is a severe cranial sensory ganglionopathy neuronopathy (ganglionopathy) involving the vestibular, facial, and trigeminal ganglia but sparing the auditory ganglia. These observations, when coupled with the known spinal dorsal root ganglionopathy in CANVAS, indicate a shared pathogenesis of its somatosensory and cranial nerve manifestations. This is the first published account of both the otopathology and neuropathology of CANVAS, a disease that involves the central as well as the peripheral nervous system.
描述神经元病伴前庭反射消失综合征(CANVAS)中导致严重、双侧、对称、选择性前庭功能丧失的病变部位。CANVAS是一种成年起病的隐性遗传性共济失调,其特征是由于小脑、躯体感觉和选择性前庭功能障碍合并存在且听力正常而导致进行性平衡失调。
对5例CANVAS患者的颞骨和脑干进行组织学检查,其中4例检查了颞骨和脑干,另1例仅检查了脑干,所有病例均由临床作者之一从诊断至死亡进行诊断和随访。
所有5例颞骨均显示前庭神经节细胞严重缺失(细胞计数为正常的3%-16%),前庭神经萎缩,而前庭感受器毛细胞和前庭核得以保留。相比之下,听觉感受器毛细胞、听觉神经节(细胞计数为正常的51%-100%)和听觉神经相对保留。此外,在2例颞骨中发现的颅感觉神经节(膝状神经节和三叉神经节)也显示严重退变。
在CANVAS中,存在一种严重的颅感觉神经节神经元病(神经节病),累及前庭、面神经和三叉神经节,但不累及听觉神经节。这些观察结果,再结合CANVAS中已知的脊髓背根神经节病,表明其躯体感觉和颅神经表现具有共同的发病机制。这是首次发表的关于CANVAS耳病理学和神经病理学的报告,CANVAS是一种累及中枢和周围神经系统的疾病。