Corticobasal degeneration with primary progressive aphasia and accentuated cortical lesion in superior temporal gyrus: Case report and review

Acta Neuropathologica

Volumn 92, Issue 5, 1996, Pages 534-539

  Ikeda, Kenji ^a,b   Akiyama, Haruhiko ^a   Iritani, Shuji ^a,b   Kase, Koichi ^a,b   Arai, Tetsuaki ^a,b   Niizato, Kazuhiro ^a,b   Kuroki, Noriomi ^a,b   Kosaka, Kenji ^a,c  

^a TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

^b TOKYO METROPOLITAN MATSUZAWA HOSPITAL   (Japan)

^c YOKOHAMA CITY UNIVERSITY   (Japan)

Author keywords

Corticobasal degeneration; Cytoskeletal abnormality; Primary progressive aphasia; Tau

Indexed keywords

TAU PROTEIN;

ADULT; APHASIA; ARTICLE; BRAIN CORTEX; BRAIN DEGENERATION; BRAIN NERVE CELL; CASE REPORT; CORPUS STRIATUM; CYTOSKELETON; DEMENTIA; FEMALE; GLIA; GLOBUS PALLIDUS; GRAY MATTER; HUMAN; HUMAN TISSUE; NEUROFIBRILLARY TANGLE; NEUROPATHOLOGY; PRIORITY JOURNAL; SILVER STAINING; SUBSTANTIA NIGRA; THALAMUS;

APHASIA, PRIMARY PROGRESSIVE; FEMALE; HUMANS; MIDDLE AGED; NERVE DEGENERATION; TEMPORAL LOBE;

EID: 0029908390     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004010050558     Document Type: Article

References (27)

1. Arima K, Uesugi H, Fujita I, Sakurai Y, Oyanagi S, Andoh S, Izumiyama Y, Inose T (1994) Corticonigral degeneration with neuronal achromasia presenting with primary progressive aphasia: ultrastructural and immunocytochemical studies. J Neurol Sci 127 : 186-197
2. Braak H, Braak E (1989) Cortical and subcortical argyrophilic grains characterize a disease associated with adult onset dementia. Neuropathol Appl Neurobiol 15 : 13-26
3. Brun A, Englund B, Gustafson L, Passant U, Mann DMA, Neary D, Snowden JS (1994) Clinical and neuropathological criteria for frontotemporal dementia. J Neurol Neurosurg Psychiatry 57 : 416-418
4. Clark AW, Manz HJ, White CL III, Lehmann J, Miller D, Coyle JT (1986) Cortical degeneration with swollen chromatolytic neurons: its relationship to Pick's disease. J Neuropathol Exp Neurol 45 : 268-284
5. Feany MB, Dickson DW (1995) Widespread cytoskeletal pathology characterizes corticobasal degeneration. Am J Pathol 146 : 1388-1396
6. Gibb WRG, Luthert PJ, Marsden CD (1989) Corticobasal degeneration. Brain 112 : 1171-1192
7. Goedert M, Spillantini MG, Jakes R, Rutherford D, Crowther RA (1989) Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease. Neuron 3 : 519-526
8. Horoupian DS, Chu PL (1994) Unusual case of corticobasal degeneration with tau/Gallyas-positive neuronal and glial tangles. Acta Neuropathol 88 : 592-598
9. Ikeda K, Akiyama H, Haga C, Kondo H, Arima K, Oda T (1994) Argyrophilic thread-like structure in corticobasal degeneration and supranuclear palsy. Neurosci Lett 174 : 157-159
10. Ikeda K, Akiyama H, Kondo H, Haga C, Tanno E, Tokuda T, Ikeda S (1995) Thorn-shaped astrocytes: possibly secondarily induced tau-positive glial fibrillary tangles. Acta Neuropathol 90 : 620-625
11. Kosaka K, Ikeda K, Kobayashi K, Mehraein P (1991) Striopallidonigral degeneration in Pick's disease: a clinicopathological study of 41 cases. J Neurol 238 : 151-160
12. Lippa CF, Smith TW, Fontneau N (1990) Corticonigral degeneration with neuronal achromasia. A clinicopathologic study of two cases. J Neurol Sci 98 : 301-310
13. Lüers T, Spatz H (1957) Picksche Krankheit. In: Scholz W (eds) Handbuch der speziellen Pathologischen Anatomie und Histologie, vol XIII/1A, Springer, Berlin Göttingen Heidelberg, pp 614-715
14. Mizukami K, Makino Y, Kobayashi K, Ikeda K, Kosaka K (1990) An autopsy case of atypical Pick's disease with sensory aphasia as an initial symptom (in Japanese) Jpn J Clin Psychiatry 32 : 899-905
15. Mori H, Nishimura M, Namba Y, Oda M (1994) Corticobasal degeneration: a disease with widespread appearance of abnormal tau and neurofibrillary tangles, and its relation to progressive supranuclear palsy. Acta Neuropathol 88 : 133-121
16. Nishimura T, Ikeda K, Akiyama H, Kondo H, Kato M, Li F, Iseki E, Kosaka K (1995) Immunohistochemical investigation of tau-positive structures in the cerebral cortex of patients with progressive supranuclear palsy. Neurosci Lett 201 : 123-126
17. Nukina N, Quan Y, Nakano I, Otomo E (1992) Widespread tau abnormality in a case of corticobasal degeneration (in Japanese). Clin Neurol 32 : 1093-1101
18. Oda T, Ikeda K, Akamatsu W, Iwabuchi K, Akiyama H, Kondo H, Seta K, Kato Y, Kogure T, Hori K, Tominaga I, Onaya M (1995) An autopsy case of corticobasal degeneration clinically misdiagnosed as Pick's disease (in Japanese). Psychiatr Neurol Jpn 97 : 757-769
19. Paulus W, Selim M (1990) Corticonigral degeneration with neuronal achromasia and basal neurofibrillary tangles (review). Acta Neuropathol 81 :89-94
20. Rebeiz JJ, Kolodny EH, Richardson EP Jr (1968) Corticodentatonigral degeneration with neuronal achromasia. Arch Neurol 18 : 20-33
21. Riley DE, Lang AE, Lewis A, Resch L, Ashby P, Hornykiewicz O, Black S (1990) Cortico-basal ganglionic degeneration. Neurology 40 : 1203-1212
22. Rinne JO, Lee MS, Thompson PD, Marsden CD (1994) Corticobasal degeneration. A clinical study of 36 cases. Brain 117 : 1183-1196
23. Uchihara T, Mitani K, Mori H, Kondo H, Yamada M, Ikeda K (1994) Abnormal cytoskeletal pathology peculiar to corticobasal degeneration is different from that of Alzheimer's disease or progressive supranuclear palsy. Acta Neuropathol 88 : 379-383
24. Wakabayashi K, Oyanagi K, Makifuchi T, Ikuta F, Homma Y, Horikawa Y, Tokiguchi S (1994) Corticobasal degeneration: etiopathological significance of the cytoskeletal alterations. Acta Neuropathol 87 : 545-553
25. Weintraub S, Rubin NP, Mesulam MM (1990) Primary progressive aphasia. Longitudinal course, neuropsychological profile, and language features. Arch Neurol 47 : 1329-1335
26. Yamada T, McGeer PL (1990) Oligodendroglial microtubular masses: an abnormality observed in some human neurodegenerative diseases. Neurosci Lett 120: 163-166
27. Yoshimura I, Yoshimura N, Hayashi S, Tasaki H, Fukushima Y (1995) A clinicopathological study of senile dementia presenting as progressive sensory aphasia; a variant of corticobasal degeneration (in Japanese). Jpn J Clin Psychiatry 24: 193-200