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Acute ascending polyradiculoneuritis in a case of Creutzfeldt-Jakob disease.

作者信息

Lope E S, Junquera S R, Martinez A M, Berenguel A B

出版信息

J Neurol Neurosurg Psychiatry. 1977 Feb;40(2):149-55. doi: 10.1136/jnnp.40.2.149.

DOI:10.1136/jnnp.40.2.149
PMID:325182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC492630/
Abstract

A patient is described who showed subacute dementia and ataxia and, finally, acute asending polyradiculoneuritis. At necropsy, together with the cerebral and cerebellar lesions that are typical of Creutzfeldt-Jakob disease, the lesions of the spinal motor neurons, the spinal ganglia, and of the roots and peripheral nerves were analogous with those of the Guillain-Barré-Landry syndrome. The aetiological possibility is discussed either that this is a simple and unique association, or that the disorder is related to the virus nature of Creutzfeldt-Jakob disease.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/c5512f941c3b/jnnpsyc00152-0050-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/11e988fa40c6/jnnpsyc00152-0047-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/faff40354513/jnnpsyc00152-0048-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/247938c30006/jnnpsyc00152-0048-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/9f0262201af7/jnnpsyc00152-0049-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/96b3134aff3d/jnnpsyc00152-0049-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/583801ced937/jnnpsyc00152-0050-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/c5512f941c3b/jnnpsyc00152-0050-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/11e988fa40c6/jnnpsyc00152-0047-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/faff40354513/jnnpsyc00152-0048-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/247938c30006/jnnpsyc00152-0048-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/9f0262201af7/jnnpsyc00152-0049-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/96b3134aff3d/jnnpsyc00152-0049-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/583801ced937/jnnpsyc00152-0050-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae9/492630/c5512f941c3b/jnnpsyc00152-0050-b.jpg

相似文献

1
Acute ascending polyradiculoneuritis in a case of Creutzfeldt-Jakob disease.
J Neurol Neurosurg Psychiatry. 1977 Feb;40(2):149-55. doi: 10.1136/jnnp.40.2.149.
2
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4
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[Adrenalitis inclusio-necroticans in the Landry-Guillain-Barré-Syndrome].[Landry - Guillain - Barré综合征中的包涵体坏死性肾上腺炎]
Dtsch Z Nervenheilkd. 1968;193(3):195-218.
8
AN ATAXIC FORM OF SUBACUTE PRESENILE POLIOENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE).一种亚急性早老性脑脊髓病(克雅氏病)的共济失调型
J Neurol Neurosurg Psychiatry. 1965 Aug;28(4):350-61. doi: 10.1136/jnnp.28.4.350.
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Syndromes of amyotrophic lateral sclerosis and dementia: relation to transmissible Creutzfeldt-Jakob disease.肌萎缩侧索硬化症与痴呆综合征:与可传播性克雅氏病的关系。
Ann Neurol. 1983 Jul;14(1):17-26. doi: 10.1002/ana.410140104.
10
Ataxic Creutzfeldt-Jakob disease: diagnostic techniques and neuropathologic observations in early disease.
Neurology. 1985 Feb;35(2):254-7. doi: 10.1212/wnl.35.2.254.

本文引用的文献

1
AN ATAXIC FORM OF SUBACUTE PRESENILE POLIOENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE).一种亚急性早老性脑脊髓病(克雅氏病)的共济失调型
J Neurol Neurosurg Psychiatry. 1965 Aug;28(4):350-61. doi: 10.1136/jnnp.28.4.350.
2
Creutzfeldt-Jakob disease (spongiform encephalopathy): transmission to the chimpanzee.克雅氏病(海绵状脑病):传播至黑猩猩。
Science. 1968 Jul 26;161(3839):388-9. doi: 10.1126/science.161.3839.388.
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Primary progressive multifocal leukoencephalopathy. A central nervous system disease caused by a slow virus.
Arch Neurol. 1972 Oct;27(4):357-60. doi: 10.1001/archneur.1972.00490160085012.
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A study of a patient with the amyotrophic form of Creutzfeldt-Jakob disease.一项关于患有肌萎缩型克雅氏病患者的研究。
Brain. 1971;94(4):715-24. doi: 10.1093/brain/94.4.715.
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[Anatomical and clinical study of a case of Creutzfeldt-Jakob disease. Ultrastructural aspects].
Rev Neurol (Paris). 1969 Aug;121(2):165-79.
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Creutzfeldt-Jakob disease. 1. Survey of the literature and clinical diagnosis.克雅氏病。1. 文献综述与临床诊断
Acta Neurol Scand. 1968;44(1):1-32. doi: 10.1111/j.1600-0404.1968.tb07440.x.
7
The clinical characteristics of transmissible Creutzfeldt-Jakob disease.可传播性克雅氏病的临床特征
Brain. 1973;96(1):1-20. doi: 10.1093/brain/96.1.1.
8
The ataxic form of Creutzfeldt-Jakob disease.克雅氏病的共济失调型
Arch Neurol. 1973 Nov;29(5):318-23. doi: 10.1001/archneur.1973.00490290058006.
9
Argentophilic plaques in Creutzfeldt-Jakob disease.克雅氏病中的嗜银斑
Arch Neurol. 1972 Jun;26(6):530-42. doi: 10.1001/archneur.1972.00490120070008.
10
Etiology of progressive multifocal leukoencephalopathy. Identification of papovavirus.进行性多灶性白质脑病的病因。乳头多瘤空泡病毒的鉴定。
N Engl J Med. 1973 Dec 13;289(24):1278-82. doi: 10.1056/NEJM197312132892405.