在一例克雅氏病患者中，症状出现前1年就发现了磁共振成像异常。 - Suppr

MRI abnormalities found 1 year prior to symptom onset in a case of Creutzfeldt-Jakob disease.

作者信息

Verde Federico, Ticozzi Nicola, Messina Stefano, Calcagno Narghes, Girotti Floriano, Maderna Luca, Moda Fabio, Scola Elisa, Falini Andrea, Tagliavini Fabrizio, Silani Vincenzo

机构信息

Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy.

Department of Pathophysiology and Transplantation, "Dino Ferrari" Centre, University of Milan Medical School, Milan, Italy.

出版信息

J Neurol. 2016 Mar;263(3):597-9. doi: 10.1007/s00415-016-8022-6. Epub 2016 Feb 12.

DOI:10.1007/s00415-016-8022-6

PMID:26872662

Abstract

摘要

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MRI abnormalities found 1 year prior to symptom onset in a case of Creutzfeldt-Jakob disease.

J Neurol. 2016 Mar;263(3):597-9. doi: 10.1007/s00415-016-8022-6. Epub 2016 Feb 12.

Early detection of familial Creutzfeldt-Jakob disease on diffusion-weighted imaging before symptom onset.

J Neurol Sci. 2012 Aug 15;319(1-2):130-2. doi: 10.1016/j.jns.2012.04.004. Epub 2012 May 27.

An autopsied case of MM1 + MM2-cortical with thalamic-type sporadic Creutzfeldt-Jakob disease presenting with hyperintensities on diffusion-weighted MRI before clinical onset.

Neuropathology. 2017 Feb;37(1):78-85. doi: 10.1111/neup.12327. Epub 2016 Jul 20.

Heidenhain variant of Creutzfeldt-Jakob disease: diffusion-weighted MRI and PET characteristics.

J Neuroimaging. 2004 Jan;14(1):63-6.

Serial diffusion-weighted MRI and SPECT findings in a Creutzfeldt-Jakob disease patient with V180I mutation.

J Neurol Sci. 2011 Feb 15;301(1-2):100-3. doi: 10.1016/j.jns.2010.10.032. Epub 2010 Nov 20.

MM1-Type Sporadic Creutzfeldt-Jakob Disease With Early Behavioral Changes and Prolonged Symptom Duration.

J Neuropsychiatry Clin Neurosci. 2016 Spring;28(2):e31-2. doi: 10.1176/appi.neuropsych.15120404.

Heidenhain variant of Creutzefeldt-Jackob disease in a patient carrying the V210I mutation with asymmetric MRI abnormalities.

Acta Neurol Belg. 2020 Aug;120(4):1007-1009. doi: 10.1007/s13760-020-01381-8. Epub 2020 May 20.

Positron emission tomography and histopathology in Creutzfeldt-Jakob disease.

Neurology. 1993 Sep;43(9):1828-30. doi: 10.1212/wnl.43.9.1828.

Serial positron emission tomography with fludeoxyglucose F 18 in Creutzfeldt-Jakob disease.

AJNR Am J Neuroradiol. 1995 Apr;16(4 Suppl):978-81.

Diffusion-weighted MR imaging of early-stage Creutzfeldt-Jakob disease: typical and atypical manifestations.

Radiographics. 2006 Oct;26 Suppl 1:S191-204. doi: 10.1148/rg.26si065503.

引用本文的文献

Significance of Cortical Ribboning as a Biomarker in the Prodromal Phase of Sporadic Creutzfeldt-Jakob Disease.

Intern Med. 2022 Sep 1;61(17):2667-2670. doi: 10.2169/internalmedicine.8354-21. Epub 2022 Feb 19.

Case Report: Extremely Early Detection of Preclinical Magnetic Resonance Imaging Abnormality in Creutzfeldt-Jakob Disease With the V180I Mutation.

Front Neurol. 2021 Oct 7;12:751750. doi: 10.3389/fneur.2021.751750. eCollection 2021.

Selective vulnerability to atrophy in sporadic Creutzfeldt-Jakob disease.

Ann Clin Transl Neurol. 2021 Jun;8(6):1183-1199. doi: 10.1002/acn3.51290. Epub 2021 May 5.

Cerebrospinal fluid and plasma biomarkers in individuals at risk for genetic prion disease.

BMC Med. 2020 Jun 18;18(1):140. doi: 10.1186/s12916-020-01608-8.

Cortical Hyperintensity on Diffusion-weighted Images as the Presymptomatic Marker of Sporadic Creutzfeldt-Jakob Disease.

Intern Med. 2019 Mar 1;58(5):727-729. doi: 10.2169/internalmedicine.1155-18. Epub 2018 Oct 17.

An In Vivo C-(R)-PK11195 PET and In Vitro Pathology Study of Microglia Activation in Creutzfeldt-Jakob Disease.

Mol Neurobiol. 2018 Apr;55(4):2856-2868. doi: 10.1007/s12035-017-0522-6. Epub 2017 Apr 28.

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Sci Rep. 2017 Apr 7;7:46269. doi: 10.1038/srep46269.

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Sporadic human prion diseases: molecular insights and diagnosis.

Lancet Neurol. 2012 Jul;11(7):618-28. doi: 10.1016/S1474-4422(12)70063-7.

Early detection of familial Creutzfeldt-Jakob disease on diffusion-weighted imaging before symptom onset.

J Neurol Sci. 2012 Aug 15;319(1-2):130-2. doi: 10.1016/j.jns.2012.04.004. Epub 2012 May 27.

Early detection of sporadic CJD by diffusion-weighted MRI before the onset of symptoms.

J Neurol Neurosurg Psychiatry. 2011 Aug;82(8):942-3. doi: 10.1136/jnnp.2008.155242. Epub 2010 Jun 11.

Diffusion weighted MR imaging in non-infarct lesions of the brain.

Eur J Radiol. 2008 Mar;65(3):402-16. doi: 10.1016/j.ejrad.2007.04.023. Epub 2007 Jun 6.

Creutzfeldt-Jakob disease: comparative analysis of MR imaging sequences.

AJNR Am J Neuroradiol. 2006 Aug;27(7):1459-62.

The MM2-cortical form of sporadic Creutzfeldt-Jakob disease presenting with visual disturbance.

Neurology. 2006 Aug 8;67(3):531-3. doi: 10.1212/01.wnl.0000228224.35678.60.

Clinical features and diagnosis of the MM2 cortical subtype of sporadic Creutzfeldt-Jakob disease.

Arch Neurol. 2006 Jun;63(6):876-80. doi: 10.1001/archneur.63.6.876.

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MRI abnormalities found 1 year prior to symptom onset in a case of Creutzfeldt-Jakob disease.

作者信息

Verde Federico, Ticozzi Nicola, Messina Stefano, Calcagno Narghes, Girotti Floriano, Maderna Luca, Moda Fabio, Scola Elisa, Falini Andrea, Tagliavini Fabrizio, Silani Vincenzo

机构信息

Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy.

Department of Pathophysiology and Transplantation, "Dino Ferrari" Centre, University of Milan Medical School, Milan, Italy.

出版信息

J Neurol. 2016 Mar;263(3):597-9. doi: 10.1007/s00415-016-8022-6. Epub 2016 Feb 12.

DOI:10.1007/s00415-016-8022-6

PMID:26872662

Abstract

摘要

相似文献

MRI abnormalities found 1 year prior to symptom onset in a case of Creutzfeldt-Jakob disease.

J Neurol. 2016 Mar;263(3):597-9. doi: 10.1007/s00415-016-8022-6. Epub 2016 Feb 12.

Early detection of familial Creutzfeldt-Jakob disease on diffusion-weighted imaging before symptom onset.

J Neurol Sci. 2012 Aug 15;319(1-2):130-2. doi: 10.1016/j.jns.2012.04.004. Epub 2012 May 27.

An autopsied case of MM1 + MM2-cortical with thalamic-type sporadic Creutzfeldt-Jakob disease presenting with hyperintensities on diffusion-weighted MRI before clinical onset.

Neuropathology. 2017 Feb;37(1):78-85. doi: 10.1111/neup.12327. Epub 2016 Jul 20.

Heidenhain variant of Creutzfeldt-Jakob disease: diffusion-weighted MRI and PET characteristics.

J Neuroimaging. 2004 Jan;14(1):63-6.

Serial diffusion-weighted MRI and SPECT findings in a Creutzfeldt-Jakob disease patient with V180I mutation.

J Neurol Sci. 2011 Feb 15;301(1-2):100-3. doi: 10.1016/j.jns.2010.10.032. Epub 2010 Nov 20.

MM1-Type Sporadic Creutzfeldt-Jakob Disease With Early Behavioral Changes and Prolonged Symptom Duration.

J Neuropsychiatry Clin Neurosci. 2016 Spring;28(2):e31-2. doi: 10.1176/appi.neuropsych.15120404.

Heidenhain variant of Creutzefeldt-Jackob disease in a patient carrying the V210I mutation with asymmetric MRI abnormalities.

Acta Neurol Belg. 2020 Aug;120(4):1007-1009. doi: 10.1007/s13760-020-01381-8. Epub 2020 May 20.

Positron emission tomography and histopathology in Creutzfeldt-Jakob disease.

Neurology. 1993 Sep;43(9):1828-30. doi: 10.1212/wnl.43.9.1828.

Serial positron emission tomography with fludeoxyglucose F 18 in Creutzfeldt-Jakob disease.

AJNR Am J Neuroradiol. 1995 Apr;16(4 Suppl):978-81.

Diffusion-weighted MR imaging of early-stage Creutzfeldt-Jakob disease: typical and atypical manifestations.

Radiographics. 2006 Oct;26 Suppl 1:S191-204. doi: 10.1148/rg.26si065503.

引用本文的文献

Significance of Cortical Ribboning as a Biomarker in the Prodromal Phase of Sporadic Creutzfeldt-Jakob Disease.

Intern Med. 2022 Sep 1;61(17):2667-2670. doi: 10.2169/internalmedicine.8354-21. Epub 2022 Feb 19.

Case Report: Extremely Early Detection of Preclinical Magnetic Resonance Imaging Abnormality in Creutzfeldt-Jakob Disease With the V180I Mutation.

Front Neurol. 2021 Oct 7;12:751750. doi: 10.3389/fneur.2021.751750. eCollection 2021.

Selective vulnerability to atrophy in sporadic Creutzfeldt-Jakob disease.

Ann Clin Transl Neurol. 2021 Jun;8(6):1183-1199. doi: 10.1002/acn3.51290. Epub 2021 May 5.

Cerebrospinal fluid and plasma biomarkers in individuals at risk for genetic prion disease.

BMC Med. 2020 Jun 18;18(1):140. doi: 10.1186/s12916-020-01608-8.

Cortical Hyperintensity on Diffusion-weighted Images as the Presymptomatic Marker of Sporadic Creutzfeldt-Jakob Disease.

Intern Med. 2019 Mar 1;58(5):727-729. doi: 10.2169/internalmedicine.1155-18. Epub 2018 Oct 17.

An In Vivo C-(R)-PK11195 PET and In Vitro Pathology Study of Microglia Activation in Creutzfeldt-Jakob Disease.

Mol Neurobiol. 2018 Apr;55(4):2856-2868. doi: 10.1007/s12035-017-0522-6. Epub 2017 Apr 28.

Detection of prion seeding activity in the olfactory mucosa of patients with Fatal Familial Insomnia.

Sci Rep. 2017 Apr 7;7:46269. doi: 10.1038/srep46269.

本文引用的文献

Sporadic human prion diseases: molecular insights and diagnosis.

Lancet Neurol. 2012 Jul;11(7):618-28. doi: 10.1016/S1474-4422(12)70063-7.

Early detection of familial Creutzfeldt-Jakob disease on diffusion-weighted imaging before symptom onset.

J Neurol Sci. 2012 Aug 15;319(1-2):130-2. doi: 10.1016/j.jns.2012.04.004. Epub 2012 May 27.

Early detection of sporadic CJD by diffusion-weighted MRI before the onset of symptoms.

J Neurol Neurosurg Psychiatry. 2011 Aug;82(8):942-3. doi: 10.1136/jnnp.2008.155242. Epub 2010 Jun 11.

Diffusion weighted MR imaging in non-infarct lesions of the brain.

Eur J Radiol. 2008 Mar;65(3):402-16. doi: 10.1016/j.ejrad.2007.04.023. Epub 2007 Jun 6.

Creutzfeldt-Jakob disease: comparative analysis of MR imaging sequences.

AJNR Am J Neuroradiol. 2006 Aug;27(7):1459-62.

The MM2-cortical form of sporadic Creutzfeldt-Jakob disease presenting with visual disturbance.

Neurology. 2006 Aug 8;67(3):531-3. doi: 10.1212/01.wnl.0000228224.35678.60.

Clinical features and diagnosis of the MM2 cortical subtype of sporadic Creutzfeldt-Jakob disease.

Arch Neurol. 2006 Jun;63(6):876-80. doi: 10.1001/archneur.63.6.876.

MRI abnormalities found 1 year prior to symptom onset in a case of Creutzfeldt-Jakob disease.

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MRI abnormalities found 1 year prior to symptom onset in a case of Creutzfeldt-Jakob disease.

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