From the University of Melbourne (D.J.S.), Royal Victorian Eye & Ear Hospital, Melbourne, Australia; Department of Anatomical Pathology (C.A.M.), Alfred Hospital, Melbourne, Australia; Department of Forensic Medicine (M.L.R.), New South Wales Pathology, New South Wales, Australia; Department of Medicine (A.M.C.), Tauranga Hospital, Wellington, New Zealand; Department of Neurology (S.M.), Capital Coast Health, Wellington, New Zealand; Pathology (D.L.), Waikato Hospital, Hamilton, Waikato, New Zealand; Department of Neuroscience (L.R.), St Vincent's Hospital, Melbourne, Australia; Department of Neuroscience (E.S.), Monash University, Melbourne, Australia; and Department of Neurology (G.M.H.), Royal Prince Alfred Hospital, Sydney, Australia.
Neurology. 2014 Apr 22;82(16):1410-5. doi: 10.1212/WNL.0000000000000352. Epub 2014 Mar 28.
To elucidate the neuropathology in cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS), a novel cerebellar ataxia comprised of the triad of cerebellar impairment, bilateral vestibular hypofunction, and a peripheral sensory deficit.
Brain and spinal neuropathology in 2 patients with CANVAS, together with brain and otopathology in another patient with CANVAS, were examined postmortem.
Spinal cord pathology demonstrated a marked dorsal root ganglionopathy with secondary tract degeneration. Cerebellar pathology showed loss of Purkinje cells, predominantly in the vermis.
The likely underlying sensory pathology in CANVAS is loss of neurons from the dorsal root and V, VII, and VIII cranial nerve ganglia-in other words, it is a "neuronopathy" rather than a "neuropathy." Clinically, CANVAS is a differential diagnosis for both spinocerebellar ataxia type 3 (or Machado-Joseph disease) and Friedreich ataxia. In addition, there are 6 sets of sibling pairs, implying that CANVAS is likely to be a late-onset recessive or autosomal dominant with reduced penetrance disorder, and identification of the culprit gene is currently a target of investigation.
阐明小脑性共济失调伴多发性神经病和双侧前庭反射消失综合征(CANVAS)的神经病理学特征。CANVAS 是一种新型小脑性共济失调,其三联征包括小脑损害、双侧前庭功能低下和周围感觉缺失。
对 2 例 CANVAS 患者的脑和脊髓神经病理学以及另 1 例 CANVAS 患者的脑和耳病理学进行了尸检检查。
脊髓病理学表现为明显的背根神经节病伴继发性神经束变性。小脑病理学显示浦肯野细胞缺失,主要位于蚓部。
CANVAS 中可能存在的感觉神经病理学是背根和颅神经 V、VII 和 VIII 神经节神经元缺失,换句话说,这是一种“神经元病”,而不是“神经病”。临床上,CANVAS 是脊髓小脑性共济失调 3 型(或 Machado-Joseph 病)和弗里德里希共济失调的鉴别诊断。此外,还有 6 对同胞对,这表明 CANVAS 可能是一种迟发性常染色体隐性或显性遗传疾病,外显率降低,目前正在寻找致病基因。