Motor neuron disease group accompanied by inclusions of unidentified protein signaled by ubiquitin

被引:6
作者
Ikeda, K
Tsuchiya, K
机构
[1] Tokyo Inst Psychiat, Dept Psychogeriat, Setagaya Ku, Tokyo 1560057, Japan
[2] Tokyo Metropolitan Matsuzawa Hosp, Setagaya Ku, Tokyo, Japan
关键词
amyotrophic lateral sclerosis; dementia; motor neuron; Pick's disease; ubiquitinated inclusion;
D O I
10.1111/j.1440-1789.2003.00537.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Peculiar tau-negative, ubiquitin-positive inclusions appear in dementia with ALS (ALS-D), the majority of lobar atrophy (Pick's disease) without Pick body and a small portion of ALS. Another common neuropathological lesion in these diseases is the motor neuron involvement with the degenerative processes. The lower motor neuron is predominantly involved in ALS and ALS-D while the upper motor neuron is predominantly involved, but in varying degrees in a considerable number of patients with lobar atrophy that lack Pick bodies. There are, however, some points that have yet to be elucidated. The boundary between these diseases is not always clear and a significant number of cases are considered to be the transitional form. Lobar atrophy without Pick body seems to be a heterogeneous disease group. The nature of ubiquitin inclusions also needs to be clarified. Nevertheless, we postulate that these diseases are grouped with the concept of motor neuron disease-inclusion dementia.
引用
收藏
页码:117 / 124
页数:8
相关论文
共 26 条
[1]   Neuronal and glial inclusions in frontotemporal dementia with or without motor neuron disease are immunopositive for p62 [J].
Arai, T ;
Nonaka, T ;
Hasegawa, M ;
Akiyama, H ;
Yoshida, M ;
Hashizume, Y ;
Tsuchiya, K ;
Oda, T ;
Ikeda, K .
NEUROSCIENCE LETTERS, 2003, 342 (1-2) :41-44
[2]   Different variants of frontotemporal dementia: A neuropathological and immunohistochemical study [J].
Bergmann, M ;
Kuchelmeister, K ;
Schmid, KW ;
Kretzschmar, HA ;
Schroder, R .
ACTA NEUROPATHOLOGICA, 1996, 92 (02) :170-179
[3]  
BRUN A, 1994, J NEUROL NEUROSUR PS, V57, P416
[4]  
HULETTE CM, 1992, CLIN NEUROPATHOL, V11, P151
[5]   Morphometrical reappraisal of motor neuron system of Pick's disease and amyotrophic lateral sclerosis with dementia [J].
Ikeda, K ;
Akiyama, H ;
Arai, T ;
Ueno, H ;
Tsuchiya, K ;
Kosaka, K .
ACTA NEUROPATHOLOGICA, 2002, 104 (01) :21-28
[6]   Neuropathological discrepancy between Japanese Pick's disease without Pick bodies and frontal lobe degeneration type of frontotemporal dementia proposed by Lund and Manchester Group [J].
Ikeda, K .
NEUROPATHOLOGY, 2000, 20 (01) :76-82
[7]  
IKEDA K, 2001, SHINKEIKENKYU NO SHI, V45, P329
[8]   Ubiquitin-immunohistochemical investigation of atypical Pick's disease without Pick bodies [J].
Iseki, E ;
Li, F ;
Odawara, T ;
Hino, H ;
Suzuki, K ;
Kosaka, K ;
Akiyama, H ;
Ikeda, K ;
Kato, M .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 159 (02) :194-201
[9]   Motor neurone disease-inclusion dementia [J].
Jackson, M ;
Lennox, G ;
Lowe, J .
NEURODEGENERATION, 1996, 5 (04) :339-350
[10]   Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions [J].
Kertesz, A ;
Kawarai, T ;
Rogaeva, E ;
St George-Hyslop, P ;
Poorkaj, P ;
Bird, TD ;
Munoz, DG .
NEUROLOGY, 2000, 54 (04) :818-827