From primary progressive aphasia to corticobasal syndrome: Two clinical and rCBF functional reports

Neurocase

Volumn 19, Issue 2, 2013, Pages 201-207

  Caso, Francesca ^a   Onofrio, F ^a   Falautano, M ^a   Todeschini, P ^a   Migliaccio, R ^b,c   Comi, G ^a   Perani, D ^a   Magnani, G ^a  

^a VITA SALUTE SAN RAFFAELE UNIVERSITY   (Italy)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c UNIVERSITÀ CATTOLICA DEL SACRO CUORE   (Italy)

Author keywords

Corticobasal syndrome; Functional imaging; Logopenic variant of primary progressive aphasia; Non fluent variant of primary progressive aphasia; Primary progressive aphasia

Indexed keywords

PROTEIN 14 3 3; TAU PROTEIN; TECHNETIUM 99M;

ADULT; AGED; ANOMIA; ARTICLE; BRAIN ATROPHY; BRAIN PERFUSION; CASE REPORT; COGNITION; COGNITIVE DEFECT; COMPUTER ASSISTED TOMOGRAPHY; CORTICOBASAL DEGENERATION; DEMENTIA; DIFFERENTIAL DIAGNOSIS; DYSGRAPHIA; ELECTROENCEPHALOGRAPHY; EVOKED MUSCLE RESPONSE; EVOKED SOMATOSENSORY RESPONSE; FEMALE; HUMAN; INTERVIEW; LANGUAGE DISABILITY; MINI MENTAL STATE EXAMINATION; MOTOR DYSFUNCTION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIMARY PROGRESSIVE APHASIA; READING; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY; SPEECH; VERBAL MEMORY;

AGED; APHASIA, PRIMARY PROGRESSIVE; CEREBROVASCULAR CIRCULATION; COGNITION DISORDERS; CYSTEINE; FEMALE; HUMANS; LONGITUDINAL STUDIES; NEUROPSYCHOLOGICAL TESTS; ORGANOTECHNETIUM COMPOUNDS; RADIOPHARMACEUTICALS; RETROSPECTIVE STUDIES; TOMOGRAPHY, EMISSION-COMPUTED, SINGLE-PHOTON;

EID: 84876134715     PISSN: 13554794     EISSN: 14653656     Source Type: Journal    
DOI: 10.1080/13554794.2012.667117     Document Type: Article

References (22)

1. Borroni, B., Garibotto, V., Agosti, C., Brambati, S. M., Bellelli, G., Gasparotti, R., Padovani, A. and Perani, D. 2008. White matter changes in corticobasal degeneration syndrome and correlation with limb apraxia. Archives of Neurology, 65(6): 796-798.
2. Boxer, A. L., Geschwind, M. D., Belfor, N., Gorno-Tempini, M. L., Schauer, G. F., Miller, B. L., Weiner, M. W. and Rosen, H. J. 2006. Patterns of brain atrophy that differentiate corticobasal degeneration syndrome from progressive supranuclear palsy. Archives of Neurology, 63: 81
3. Buxbaum, L. J., Kyle, K., Grossman, M. and Coslett, H. B. 2007. Left inferior parietal representations for skilled hand-object interactions: Evidence from stroke and corticobasal degeneration. Cortex, 43(3): 411-423.
4. Goldenberg, G. 2009. Apraxia and the parietal lobes. Neuropsychologia, 47(6): 1449-1459.
5. Gorno-Tempini, M. L., Dronkers, N. F., Rankin, K. P., Ogar, J. M., Phengrasamy, La, Rosen, H. J., Johnson, J. K., Weiner, M. W. and Miller, B. L. 2004. Cognition and anatomy in three variants of primary progressive aphasia. Ann of Neurology, 55(3): 335-346.
6. Gorno-Tempini, M. L., Hillis, A. E., Weintraub, S., Kertesz, A., Mendez, M., Cappa, S. F., Ogar, J. M., Rohrer, J. D., Black, S.Boeve, B. F. 2011. Classification of primary progressive aphasia and its variants. Neurology, 76(11): 1006-1014.
7. Graham, N. L., Bak, T., Patterson, K. and Hodges, J. R. 2003. Language function and dysfunction in corticobasal degeneration. Neurology, 61: 493-499.
8. Kertesz, A., Martinez-Lage, P., Davidson, W. and Munoz, D. G. 2000. The corticobasal degeneration syndrome overlaps progressive aphasia and frontotemporal dementia. Neurology, 55: 1368-1375.
9. Josephs, K. A., Hodges, J. R., Snowden, J. S., Mackenzie, I. R., Neumann, M., Mann, D. M. and Dickson, D. W. 2011. Neuropathological background of phenotypicalvariability in frontotemporaldementia. Acta Neuropathologica, 122: 137-153.
10. Josephs, K. A., Petersen, R. C., Knopman, D. S., Boeve, B. F., Whitwell, J. L., Duffy, J. R., Parisi, J. E. and Dickson, D. W. 2006. Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP. Neurology, 66: 41-48.
11. Lee, S. E., Rabinovici, G. D., Mayo, M. C., Wilson, S. M., Seeley, W. W., DeArmond, S. J., Huang, E. J., Trojanowski, J. Q., Growdon, M. E.Jang, J. Y. 2011. Clinicopathological correlations in corticobasal degeneration. Annals of Neurology, 70(2): 327-340.
12. Mahapatra, R. K., Edwards, M. J., Schott, J. M. and Bhatia, K. P. 2004. Corticobasal degeneration. Lancet Neurology, 3(12): 736-743.
13. McMonagle, P., Blair, M. and Kertesz, A. 2006. Corticobasal degeneration and progressive aphasia. Neurology, 67: 1444-1451.
14. McNeil, M. R., Robin, D. A. and Schmidt, R. A. 2009. "Apraxia of speech: Definition, differentiation, and treatment". In Clinical management of sensorimotor speech disorders, 2nd, Edited by: McNeil, M. R. 249-268. New York, NY: Thieme.
15. Mesulam, M. M. 2001. Primary progressive aphasia. Annals of Neurology, 49: 425-432.
16. Mesulam, M., Wicklund, A., Johnson, N., Rogalski, E., Leger, G. C., Rademaker, A., Weintraub, S. and Bigio, E. H. 2008. Alzheimer and frontotemporalpathology in subsets of primary progressive aphasia. Annals of Neurology, 63: 709-719.
17. Migliaccio, R., Agosta, F., Rascovsky, K., Karydas, A., Bonasera, S., Rabinovici, G. D., Miller, B. L. and Gorno-Tempini, M. L. 2009. Clinical syndromes associated with posterior atrophy: Early age at onset AD spectrum. Neurology, 73(19): 1571-1578.
18. Neary, D., Snowden, J. and Mann, D. 2005. Frontotemporaldementia. Lancet Neurology, 4(11): 771-780.
19. Peigneux, P., Salmon, E., Garraux, G., Laureys, S., Willems, S., Dujardin, K., Degueldre, C., Lemaire, C., Luxen, A.Moonen, G. 2001. Neural and cognitive bases of upperlimbapraxia in corticobasaldegeneration. Neurology, 57(7): 1259-1268.
20. Rohrer, J. D., Geser, F., Zhou, J., Gennatas, E. D., Sidhu, M., Trojanowski, J. Q., Dearmond, S. J., Miller, B. L. and Seeley, W. W. 2010. TDP-43 subtypes are associatedwith distinct atrophy patterns in frontotemporal dementia. Neurology, 75(24): 2204-2211.
21. Spina, S., Murrell, J. R., Huey, E. D., Wassermann, E. M., Pietrini, P., Grafman, J. and Ghetti, B. 2007. Corticobasal syndrome associated with the A9D progranulin mutation. Journal of Neuropathology & Experimental Neurology, 66(10): 892-900.
22. Van Swieten, J. C. and Heutink, P. 2008. Mutations in progranulin (GRN) within the spectrum of clinical and pathologicalphenotypes of frontotemporaldementia. Lancet Neurology, 7(10): 965-974.