An 81-year-old man with imbalance and memory impairment

An 81-year-old man presented for evaluation of balance difficulties and nocturia. From January 1994 through February 1995, he developed progressive dizziness, which he described as a feeling of imbalance or unsteadiness when walking. This sensation occurred independently of changes in position and was not associated with true vertigo. His symptoms were identified shortly after he underwent knee surgery that was complicated by a gastrointestinal bleed requiring a blood transfusion. Over the year, his symptoms progressively worsened; he required a cane due to frequent falls and he lost interest in hunting, fishing, and reading. He developed increased rumination and anxiety with obsessive/compulsive behaviors that included the need to draw blinds, lock doors, or take out the trash immediately upon thinking of these actions. On a daily basis, he would sit at the window waiting for the mail to arrive and had to be the first one to retrieve and open it once it arrived. From March 1995 through February 1996, the patient’s wife noted he was becoming more forgetful and impatient. She took over the household finances by this time. Local evaluation included a head CT scan that by report demonstrated diffuse atrophy and he was diagnosed with Alzheimer disease (AD). A 4-week trial of tacrine hydrochloride was not beneficial. He continued to drive a motor vehicle and reported no traffic violations or motor vehicle accidents. His medical history was remarkable for atrial fibrillation, hypertension, and benign prostatic hyperplasia. His medications included fluoxetine, probenecid, and terazosin, the last of which was discontinued in March 1996. His social history was remarkable for moderate alcohol intake. He did not use tobacco. His family history was negative for gait, cognitive, or other neurologic disorders. Review of symptoms was remarkable for recent complaints of lightheadedness, which was non-positional, and nocturia (three times nightly). He denied …

[1]  M. Greicius,et al.  Non-Fluent Progressive Aphasia, Depression, and OCD in a Woman With Progressive Supranuclear Palsy: Neuroanatomical and Neuropathological Correlations , 2006, Neurocase.

[2]  D. Dickson,et al.  The relationship between histopathological features of progressive supranuclear palsy and disease duration. , 2006, Parkinsonism & related disorders.

[3]  Joseph James Duffy,et al.  Atypical progressive supranuclear palsy underlying progressive apraxia of speech and nonfluent aphasia , 2005, Neurocase.

[4]  A. Lees,et al.  Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism. , 2005, Brain : a journal of neurology.

[5]  D. Burn Commentary on: Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism, by D. Williams, R. de Silva, D. Paviour, et al. (Brain-2004-01045.R1). , 2005, Brain : a journal of neurology.

[6]  E. Cochran,et al.  Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders , 2004 .

[7]  K. Arai,et al.  Study of the rostral midbrain atrophy in progressive supranuclear palsy , 2003, Journal of the Neurological Sciences.

[8]  M. Hallett,et al.  Randomized placebo-controlled trial of donepezil in patients with progressive supranuclear palsy , 2001, Neurology.

[9]  C. Colosimo,et al.  Donepezil in the treatment of progressive supranuclear palsy , 2001, Acta neurologica Scandinavica.

[10]  F. Tison,et al.  Oral zolmitriptan is effective in the acute treatment of cluster headache , 2000, Neurology.

[11]  I Litvan,et al.  Association of an extended haplotype in the tau gene with progressive supranuclear palsy. , 1999, Human molecular genetics.

[12]  M. Hallett,et al.  Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) , 1996, Neurology.

[13]  I Litvan,et al.  Preliminary NINDS neuropathologic criteria for Steele‐Richardson‐Olszewski syndrome (progressive supranuclear palsy) , 1994, Neurology.

[14]  R. Leigh,et al.  The syndrome of 'pure akinesia' and its relationship to progressive supranuclear palsy , 1994, Neurology.

[15]  E. Tangalos,et al.  The short test of mental status. Correlations with standardized psychometric testing. , 1991, Archives of neurology.

[16]  A. Delacourte,et al.  Abnormal Tau proteins in progressive supranuclear palsy , 1991, Acta Neuropathologica.

[17]  L. Golbe,et al.  Prevalence and natural history of progressive supranuclear palsy , 1988, Neurology.

[18]  K P Offord,et al.  A short test of mental status: description and preliminary results. , 1987, Mayo Clinic proceedings.

[19]  F Lhermitte,et al.  Heterogeneity of cognitive impairment in progressive supranuclear palsy, Parkinson's disease, and Alzheimer's disease , 1986, Neurology.

[20]  B. Troost,et al.  The ocular motor defects in progressive supranuclear palsy , 1977, Annals of neurology.

[21]  H. Braak,et al.  Neuropathological stageing of Alzheimer-related changes , 2004, Acta Neuropathologica.

[22]  Irene Litvan,et al.  Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia , 2003, Annals of neurology.