Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease

被引:49
作者
Haïk, S
Brandel, JP
Sazdovitch, V
Delasnerie-Lauprêtre, N
Peoc'h, K
Laplanche, JL
Privat, N
Duyckaerts, C
Kemeny, JL
Kopp, N
Laquerrière, A
Mohr, M
Deslys, JP
Dormont, D
Hauw, JJ
机构
[1] Hop La Pitie Salpetriere, Lab Neuropathol R Escourolle, F-75013 Paris, France
[2] Hop La Pitie Salpetriere, Assoc Claude Bernard INSERM U 360, F-75013 Paris, France
[3] Hop La Pitie Salpetriere, INSERM U 106, F-75013 Paris, France
[4] Gabriel Montpied Hosp, Serv Anat Pathol, Clermont Ferrand, France
[5] Pierre Wertheimer Hosp, Lab Diagnost Malad Prion, Lyon, France
[6] Hop Charles Nicolle, Lab Anat & Cytol Pathol, Rouen, France
[7] Fac Med Strasbourg, Inst Pathol, Strasbourg, France
[8] Lariboisiere Hosp, Assoc Claude Bernard, Cent Lab Biochem, Paris, France
[9] CRSSA, DRM,DSV, CEA, Serv Neurovirol, Fontenay Aux Roses, France
关键词
D O I
10.1212/WNL.55.9.1401
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Discriminating Creutzfeldt-Jakob disease (CJD) from dementia with Lewy bodies (DLB) may be clinically difficult to achieve. The authors describe 10 patients with DLB initially referred to the French Network of Human Spongiform Encephalopathies as having suspected CJD. In a series of 465 autopsied cases, DLB ranked second among degenerative alternative diagnoses to CJD. The authors analyzed the factors that contributed to misleading the diagnosis, and suggest that the detection of 14-3-3 protein in CSF may be useful to distinguish CJD from DLB.
引用
收藏
页码:1401 / 1404
页数:4
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