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成人起病的神经元核内包涵体病的诊断指标。

Diagnostic indicators for adult-onset neuronal intranuclear inclusion disease.

作者信息

Wang Yan, Wang Bo, Wang Lu, Yao Sheng, Zhao Jing, Zhong Shanshan, Cong Lu, Liu Ling, Zhang Jiewen, Zhang Jun, Hong Daojun

出版信息

Clin Neuropathol. 2020 Jan/Feb;39(1):7-18. doi: 10.5414/NP301203.

DOI:10.5414/NP301203
PMID:31661069
Abstract

Adult-onset neuronal intranuclear inclusion disease (NIID) is a rare neurodegenerative disorder. Abnormally high signals of diffusion-weighted image (DWI) along the corticomedullary junction are a useful diagnostic indicator for patients with adult-onset NIID. However, the DWI abnormalities usually were observed in the late stage of disease; further study might be helpful to elucidate some clinical indicators regarding the early awareness of NIID. In this study, we summarized 9 patients with NIID from multiple centers. The mean age was 60.0 ± 6.2 years. The mean duration of disease was 4.4 ± 3.2 years. The most common symptoms included cognitive impairment, episodic encephalopathy, and bladder dysfunction. Among the 6 patients with bladder dysfunction, 3 patients had the symptom prior to the development of other neurological symptoms; 5 patients needed permanent cystostomy. Isolated high DWI signals on the splenium of corpus callosum were observed in 2 patients at the early stage. The characteristic intranuclear inclusions in the skin were identified in all patients and confirmed by electron microscopy. Episodic encephalopathy or bladder dysfunction prior to other neurological symptoms were valuable diagnostic indicators for adult-onset NIID. High DWI signals on the splenium of corpus callosum might be an early indicator for the diagnosis of NIID. The immunostain of anti-ubiquitin or anti-p62 antibody was a convenient and sensitive biomarker for NIID with the background of typical phenotype with cognitive impairment and autonomic dysfunctions.

摘要

成人起病的神经元核内包涵体病(NIID)是一种罕见的神经退行性疾病。沿皮质髓质交界区的扩散加权成像(DWI)异常高信号是成人起病NIID患者的有用诊断指标。然而,DWI异常通常在疾病晚期才被观察到;进一步研究可能有助于阐明一些关于NIID早期识别的临床指标。在本研究中,我们总结了来自多个中心的9例NIID患者。平均年龄为60.0±6.2岁。平均病程为4.4±3.2年。最常见的症状包括认知障碍、发作性脑病和膀胱功能障碍。在6例膀胱功能障碍患者中,3例在出现其他神经症状之前就有该症状;5例患者需要永久性膀胱造瘘术。2例患者在疾病早期观察到胼胝体压部孤立的高DWI信号。所有患者均在皮肤中发现特征性核内包涵体,并经电子显微镜证实。在出现其他神经症状之前的发作性脑病或膀胱功能障碍是成人起病NIID的有价值诊断指标。胼胝体压部的高DWI信号可能是NIID诊断的早期指标。抗泛素或抗p62抗体免疫染色是NIID的一种方便且敏感的生物标志物,其背景为具有认知障碍和自主神经功能障碍的典型表型。

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