肝豆状核变性的神经影像学表现

doi:10.16138/j.1673-6087.2021.05.004

摘要/Abstract

中图分类号:

谢安木, 栾梦葶, 王莹, 石万达. 肝豆状核变性的神经影像学表现[J]. 内科理论与实践, 2021, 16(05): 304-307.

参考文献 38

[1]	Xie JJ, Wu ZY. Wilson’s disease in China[J]. Neurosci Bull, 2017, 33(3): 323-330. doi: 10.1007/s12264-017-0107-4 URL
[2]	Taly AB, Meenakshi-Sundaram S, Sinha S, et al. Wilson disease: description of 282 patients evaluated over 3 decades[J]. Medicine (Baltimore), 2007, 86(2): 112-121. doi: 10.1097/MD.0b013e318045a00e URL
[3]	Członkowska A, Litwin T, Dusek P, et al. Wilson disease[J]. Nat Rev Dis Primers, 2018, 4(1): 21. doi: 10.1038/s41572-018-0018-3 pmid: 30190489
[4]	Członkowska A, Rodo M, Gromadzka G. Late onset Wilson’s disease: therapeutic implications[J]. Mov Disord, 2008, 23(6): 896-898. doi: 10.1002/mds.21985 URL
[5]	Poujois A, Woimant F. Wilson’s disease: a 2017 update[J]. Clin Res Hepatol Gastroenterol, 2018, 42(6): 512-520. doi: 10.1016/j.clinre.2018.03.007 URL
[6]	Hermann W. Morphological and functional imaging in neurological and non-neurological Wilson’s patients[J]. Ann N Y Acad Sci, 2014, 1315: 24-29. doi: 10.1111/nyas.12343 URL
[7]	Hermann W. Classification and differential diagnosis of Wilson’s disease[J]. Ann Transl Med, 2019, 7 Suppl 2: S63.
[8]	董兴伟. 磁共振对肝豆状核变性的诊断价值[J]. 中国现代药物应用, 2015, 9(1): 59-60.
[9]	Dohan A, Vargas O, Dautry R, et al. MR imaging features of focal liver lesions in Wilson disease[J]. Abdom Radiol (NY), 2016, 41(9): 1811-1824.
[10]	何望生, 杨文明. 3例肝豆状核变性的罕见脑部影像学表现[C]// 2017全国中医民族医脑病学术大会暨脑血管病和运动障碍疾病高峰论坛、第四届皖江脑病论坛. 2017: 336-339.
[11]	Sinha S, Taly AB, Ravishankar S, et al. Wilson’s disease: cranial MRI observations and clinical correlation[J]. Neuroradiology, 2006, 48(9): 613-621. pmid: 16752136
[12]	张金昌, 李志章, 时文伟. 5例肝豆状核变性患者的影像学检查结果分析[J]. 山东医药, 2005, 45(20): 53-54.
[13]	Nazer H, Brismar J al-Kawi MZ, et al. Magnetic resonance imaging of the brain in Wilson’s disease[J]. Neuro-radiology, 1993, 35(2): 130-133.
[14]	Zou L, Song Y, Zhou X, et al. Regional morphometric abnormalities and clinical relevance in Wilson’s disease[J]. Mov Disord, 2019, 34(4): 545-554. doi: 10.1002/mds.27641 URL
[15]	Prashanth LK, Sinha S, Taly AB, et al. Do MRI features distinguish Wilson’s disease from other early onset extrapyramidal disorders? An analysis of 100 cases[J]. Mov Disord, 2010, 25(6): 672-678. doi: 10.1002/mds.22689 URL
[16]	Horoupian DS, Sternlieb I, Scheinberg IH. Neuropathological findings in penicillamine-treated patients with Wilson’s disease[J]. Clin Neuropathol, 1988, 7(2): 62-67. pmid: 3390974
[17]	Bandmann O, Weiss KH, Kaler SG. Wilson’s disease and other neurological copper disorders[J]. Lancet Neurol, 2015, 14(1): 103-113. doi: 10.1016/S1474-4422(14)70190-5 pmid: 25496901
[18]	马平, 郑彬. 肝豆状核变性颅内病变的影像及临床表现[J]. 医学影像学杂志, 2018, 28(2): 326-328.
[19]	Kalita J, Kumar N, Maurya PK, et al. A study of computed tomography scan and magnetic resonance imaging findings in pseudohypoparathyroidism[J]. Ann Indian Acad Neurol, 2010, 13(3): 204-206. doi: 10.4103/0972-2327.70870 URL
[20]	Sonam K, Bindu PS, Gayathri N, et al. The “double panda” sign in Leigh disease[J]. J Child Neurol, 2014, 29(7): 980-982. doi: 10.1177/0883073813484968 URL
[21]	Trocello JM, Woimant F, El Balkhi S, et al. Extensive striatal, cortical, and white matter brain MRI abnormalities in Wilson disease[J]. Neurology, 2013, 81(17): 1557. doi: 10.1212/WNL.0b013e3182a95883 URL
[22]	Hermann W, Günther P, Hahn S, et al. Cerebral MRI and evoked potentials in Wilson disease[J]. Nervenarzt, 2002, 73(4): 349-354. pmid: 12040983
[23]	Schlaug G, Hefter H, Engelbrecht V, et al. Neurological impairment and recovery in Wilson’s disease: evidence from PET and MRI[J]. J Neurol Sci, 1996, 136(1-2): 129-139. doi: 10.1016/0022-510x(95)00293-b pmid: 8815159
[24]	Barthel H, Sorger D, Kühn HJ, et al. Differential alteration of the nigrostriatal dopaminergic system in Wilson’s disease investigated with [123I]β-CIT and high-resolution SPET[J]. Eur J Nucl Med, 2001, 28(11): 1656-1663. pmid: 11702107
[25]	Roberts EA. Update on the diagnosis and management of Wilson disease[J]. Curr Gastroenterol Rep, 2018, 20(12): 56. doi: 10.1007/s11894-018-0660-7 pmid: 30397835
[26]	Zhong W, Huang Z, Tang X. A study of brain MRI characteristics and clinical features in 76 cases of Wilson’s disease[J]. J Clin Neurosci, 2019, 59: 167-174. doi: S0967-5868(18)30210-8 pmid: 30385165
[27]	Rossi M, Ruottinen H, Soimakallio S, et al. Clinical MRI for iron detection in Parkinson’s disease[J]. Clin Imaging, 2013, 37(4): 631-636. doi: 10.1016/j.clinimag.2013.02.001 URL
[28]	Zhou XX, Qin HL, Li XH, et al. Characterizing brain mineral deposition in patients with Wilson disease using susceptibility-weighted imaging[J]. Neurol India, 2014, 62(4): 362-366. doi: 10.4103/0028-3886.141221 URL
[29]	Mittal S, Wu Z, Neelavalli J, et al. Susceptibility-weighted imaging: technical aspects and clinical applications, part 2[J]. AJNR Am J Neuroradiol, 2009, 30(2): 232-252. doi: 10.3174/ajnr.A1461 URL
[30]	Hingwala DR, Kesavadas C, Thomas B, et al. Susceptibility weighted imaging in the evaluation of movement disorders[J]. Clin Radiol, 2013, 68(6): e338-e348. doi: 10.1016/j.crad.2012.12.003 URL
[31]	Lee JH, Yang TI, Cho M, et al. Widespread cerebral cortical mineralization in Wilson’s disease detected by susceptibility-weighted imaging[J]. J Neurol Sci, 2012, 313(1-2): 54-56. doi: 10.1016/j.jns.2011.09.031 URL
[32]	Tinaz S, Arora J, Nalamada K, et al. Structural and functional brain changes in hepatic and neurological Wilson disease[J]. Brain Imaging Behav, 2020.[Epub ahead of print].
[33]	Haacke EM, Liu S, Buch S, et al. Quantitative susceptibility mapping: current status and future directions[J]. Magn Reson Imaging, 2015, 33(1): 1-25. doi: 10.1016/j.mri.2014.09.004 pmid: 25267705
[34]	Fritzsch D, Reiss-Zimmermann M, Trampel R, et al. Seven-tesla magnetic resonance imaging in Wilson disease using quantitative susceptibility mapping for measurement of copper accumulation[J]. Invest Radiol, 2014, 49(5): 299-306. doi: 10.1097/RLI.0000000000000010 pmid: 24220252
[35]	Tondo G, Esposito M, Dervenoulas G, et al. Hybrid PET-MRI applications in movement disorders[J]. Int Rev Neurobiol, 2019, 144: 211-257.
[36]	Hermann W, Barthel H, Hesse S, et al. Comparison of clinical types of Wilson’s disease and glucose metabolism in extrapyramidal motor brain regions[J]. J Neurol, 2002, 249(7): 896-901. pmid: 12140675
[37]	Hawkins RA, Mazziotta JC, Phelps ME. Wilson’s disease studied with FDG and positron emission tomography[J]. Neurology, 1987, 37(11): 1707-1711. pmid: 3499583
[38]	Hegde S, Sinha S, Rao SL, et al. Cognitive profile and structural findings in Wilson’s disease: a neuropsychological and MRI-based study[J]. Neurol India, 2010, 58(5): 708-713. doi: 10.4103/0028-3886.72172 URL

肝豆状核变性的神经影像学表现

RichHTML

PDF (PC)

可视化

摘要/Abstract

引用本文

使用本文

参考文献 38

相关文章 15

编辑推荐

Metrics

本文评价

[1]	王训, 韩咏竹, 杨任民. 肝豆状核变性的中西医药物治疗概况[J]. 内科理论与实践, 2021, 16(05): 294-298.
[2]	洪铭范. 肝豆状核变性的超声诊断[J]. 内科理论与实践, 2021, 16(05): 299-303.
[3]	周香雪, 黄海威. 肝豆状核变性影像学研究进展[J]. 内科理论与实践, 2021, 16(05): 308-314.
[4]	洪培伟, 丛雪, 徐严明. 2005至2020年中国西南地区肝豆状核变性住院费用影响因素分析[J]. 内科理论与实践, 2021, 16(05): 315-318.
[5]	黄清, 王刚. 106例肝豆状核变性的临床表型和生存期研究[J]. 内科理论与实践, 2021, 16(05): 319-324.
[6]	姚碧莲, 张欣欣, 韩悦. 肝豆状核变性的基因诊断研究进展[J]. 内科理论与实践, 2021, 16(05): 354-358.
[7]	王晓平, 吴亦影. 试谈肝豆状核变性的几个历史典故[J]. 内科理论与实践, 2021, 16(05): 359-360.
[8]	李建平, 王刚. 铜代谢稳态失调与神经退行性疾病的相关性研究进展[J]. 内科理论与实践, 2021, 16(05): 361-365.
[9]	李洵桦. 肝豆状核变性的内科治疗[J]. 内科理论与实践, 2021, 16(05): 289-293.
[10]	余舒文, 方正滢, 谢静远. 基因检测在慢性肾脏病诊治中的应用及进展[J]. 诊断学理论与实践, 2020, 19(06): 613-617.
[11]	李牛, 王剑. 精准医学时代遗传性疾病的分子诊断[J]. 诊断学理论与实践, 2018, 17(02): 136-140.
[12]	刘芸野, 谷雷雷, 黄道, 林之莓,. 肝豆状核变性的临床特征及其分子诊断[J]. 诊断学理论与实践, 2014, 13(03): 267-270.
[13]	吕建新, 张杰,. 线粒体遗传性疾病的基因诊断[J]. 诊断学理论与实践, 2013, 12(04): 381-386.
[14]	蒋黎敏, 张晓青, 钱一磊, 傅启华,. Wilson病ATP7B基因突变检测[J]. 诊断学理论与实践, 2013, 12(04): 406-409.
[15]	陈曦, 李宏为,. 遗传性胰腺神经内分泌肿瘤的认知[J]. 外科理论与实践, 2011, 16(05): 440-443.