Wang Hongfen, Feng Feng, Liu Jiajin, Deng Jianwen, Bai Jiongming, Zhang Wei, Wang Luning, Xu Baixuan, Huang Xusheng
Department of Neurology, First Medical Center, Chinese PLA General Hospital, Beijing, China.
Department of Neurology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
BMC Neurol. 2022 Apr 22;22(1):150. doi: 10.1186/s12883-022-02673-7.
Neuronal intranuclear inclusion disease (NIID) is a rare neurodegenerative disease characterized by eosinophilic hyaline intranuclear inclusions in cells in the central and peripheral nervous system. High-intensity signal in the corticomedullary junction on diffusion-weighted imaging (DWI) is supportive to the diagnosis of NIID. We describe a patient with sporadic adult-onset NIID but without any high-intensity signal on DWI and T2-weighted imaging (T2WI).
A 58-year-old woman without special family history developed mild persistent tremor in the right hand and deteriorated 2 years later. At 60 years of age, the patient began to conceive the bank, police and internet being deceptive, further presented apathy and confusion after two and a half years, as well as fabrication of non-existent things. Despite the treatment of antipsychotic drugs due to a diagnosis of mental disorder, the patient appeared weakness in the right limbs. Neurological examination revealed mutism, resting tremor, cogwheel-like rigidity in upper limbs, and weakness in all limbs. Brain magnetic resonance imaging displayed no cerebral atrophy initially but atrophy of frontal, temporal and parietal lobes 5 years later. No any high-intensity signal on DWI and T2WI was revealed. However, hypometabolism in the cortexes with atrophy and the right putamen nucleus were showed on F-fluoro-deoxy-glucose positron emission tomography/magnetic resonance. On the basis of 107 GGC repeats (normal number <40) in NOTCH2NLC gene and intranuclear inclusions with p62 immunoreactivity in the adipocyte of cutaneous sweat duct by skin biopsy, NIID was finally diagnosed. The symptomatic treatment was given but the patient had no evident improvement.
Our case highlights that despite the lack of high-intensity signal on DWI and T2WI, NIID is still considered for patients with parkinsonism and mental impairment.
神经元核内包涵体病(NIID)是一种罕见的神经退行性疾病,其特征是中枢和周围神经系统细胞中出现嗜酸性透明核内包涵体。扩散加权成像(DWI)上皮质髓质交界处的高强度信号有助于NIID的诊断。我们描述了一名散发性成人发病的NIID患者,但在DWI和T2加权成像(T2WI)上没有任何高强度信号。
一名58岁无特殊家族史的女性右手出现轻度持续性震颤,2年后病情恶化。60岁时,患者开始认为银行、警察和互联网具有欺骗性,两年半后进一步出现冷漠和混乱,以及虚构不存在的事情。尽管因精神障碍诊断接受了抗精神病药物治疗,但患者右肢出现无力。神经检查显示缄默、静止性震颤、上肢齿轮样强直和四肢无力。脑磁共振成像最初未显示脑萎缩,但5年后额叶、颞叶和顶叶出现萎缩。DWI和T2WI上未显示任何高强度信号。然而,F-氟脱氧葡萄糖正电子发射断层扫描/磁共振显示萎缩皮质和右侧壳核低代谢。基于NOTCH2NLC基因中107个GGC重复序列(正常数量<40)以及皮肤活检显示皮肤汗腺导管脂肪细胞中具有p62免疫反应性的核内包涵体,最终诊断为NIID。给予了对症治疗,但患者无明显改善。
我们的病例强调,尽管DWI和T2WI上缺乏高强度信号,但对于患有帕金森综合征和精神障碍的患者仍应考虑NIID。