[A Parietal Form of Pick's Disease: Clinical and Pathological Study (author's Transl)]
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A patient developed a neurological disorder at the age of 57 years and died 9 years later after progressive aggravation. The clinical picture was that of a unilateral, parietal, focal neurological syndrome for many years, finally becoming bilateral. The purely neurological nature of the condition, without signs of mental disturbance, should be emphasized. Pathological examination showed mainly unilateral circumscribed cortical atrophy in the parietal regions. Histological examination showed atrophic lesions typical of Pick's disease. This case provides suggestive evidence for the existence of purely parietal forms of Pick's disease.
Posterior cortical atrophy: variant of Alzheimer's disease? A case series with PET findings.
Schmidtke K, Hull M, Talazko J J Neurol. 2005; 252(1):27-35.
PMID: 15654552 DOI: 10.1007/s00415-005-0594-5.
Mathuranath P, Xuereb J, Bak T, Hodges J J Neurol Neurosurg Psychiatry. 2000; 68(3):304-12.
PMID: 10675211 PMC: 1736839. DOI: 10.1136/jnnp.68.3.304.
Slowly progressive apraxia: two case studies.
Azouvi P, Bergego C, Robel L, Marlier N, Durand I, HELD J J Neurol. 1993; 240(6):347-50.
PMID: 8336174 DOI: 10.1007/BF00839965.
Hof P, Bouras C, Perl D, Morrison J Acta Neuropathol. 1994; 87(2):115-24.
PMID: 8171960 DOI: 10.1007/BF00296179.
Striatonigral degeneration, olivopontocerebellar atrophy and "atypical" Pick disease.
Horoupian D, Dickson D Acta Neuropathol. 1991; 81(3):287-95.
PMID: 1711756 DOI: 10.1007/BF00305870.