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Mohammed T. Abou-Saleh

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296 PRINCIPLES AND PRACTICE OF GERIATRIC PSYCHIATRYfew conditions of relevance in old age psychiatry, which will beoutlined briefly. Systemic carcinomas may produce effects in thebrain by several mechanisms through metabolic disturbances(such as excess secretion of adrenocorticotrophic hormone orantidiuretic hormone), through structural change (cerebralsecondaries or infections) or through remote effect (limbicencephalitis). This last condition is common in men, particularlywith oat cell carcinomas of the lung, and has a course of up to 24months. Affective changes dominate the picture, with amnesia theprimary (and occasionally the sole) abnormality. Diagnosis of thecondition is through attention to the physical condition of theindividual. Vitamin deficiencies (notably B 12 and folate) causemental impairment, but routine testing for their levels makes thediagnosis relatively easy. The same holds true for thyroiddysfunction and hypercalcaemia. Chronic excessive alcohol intakecan result in a dementia 24 .CREUTZFELDT–JAKOB DISEASEEarly features include fatigue and listlessness, elevated mood andimpaired memory and concentration. Motor abnormalities occurwith spasticity, ataxia and tremor. Myoclonic jerks and seizuresmay occur. The EEG is very abnormal, with characteristictriphasic waves superimposed on some suppression of thebackground rhythms. The course of the illness is very rapid andmost affected individuals are dead within 2 years 25 .SUMMARYThe differential diagnosis of dementia is a two-stage process: first,the differentiation of dementia from other causes of cognitiveimpairment; and second, if it is found to be a form of dementia,the elucidation of the aetiology. Alzheimer’s disease is thecommonest form of dementia, cerebrovascular disease is probablythe second commonest cause and Lewy body dementia isbecoming increasingly recognized. The differential diagnosis ofdementia is an excellent example of how simple logical clinicalskills can be applied without the need for expensive investigations,which should be reserved for situations where there is clinicaldoubt about the diagnosis.REFERENCES1. Ritchie K, Touchon J et al. Mild cognitive impairment: conceptualbasis and current nosological status. Lancet 2000; 355: 225–8.2. Corry-Bloom J, Thal L, Galasko D et al. Diagnosis and evaluation ofdementia. Neurology 1995; 45: 211–18.3. McKhann G, Drachman D, Folstein M et al. Clinical diagnosis ofAlzheimer’s disease. Neurology 1984; 34: 939–44.4. Blessed G. Definitions and classification of the dementias.Interdisciplinary Topics in Gerontology, vol 26: Innovative Trends inPsychogeriatrics. Basel: Karger, 1989.5. Clarfield AM. The reversible dementias: do they reverse? Ann InternMed 1988; 109: 476–86.6. Walstra G, Teunisse S, van Gool W, Crevel H. Reversible dementia inelderly patients referred to a memory clinic. 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The course of geriatricdepression with reversible dementia. Am J Psychiat 1993; 150: 1693–9.15. Hachinski V, Iliff I, Zilhka E et al. Cerebral blood flow in dementia.Arch Neurol 1975; 32: 632–7.16. Chiu H, Victoroff J, Margolin et al. Criteria for the diagnosis ofischaemic vascular dementia. Neurology 1992; 42: 473–80.17. Roman G, Tatemechi T, Erkinjuntti T et al. Vascular dementia:diagnostic criteria for research studies. Neurology 1993; 43: 250–60.18. Chiu H. Huntington’s disease. In Burns A, Levy R, eds, Dementia.London: Chapman & Hall, 1994; 713–62.19. Cummings J, Duchene L. The Kluver–Bucy syndrome in Pick’sdisease. Neurology 1981; 31: 145–52.20. Neary D, Snowdon J, Northen B et al. Dementia of frontal lobe type.J Neurol Neurosurg Psychiat 1988; 51: 353–61.21. Neary D et al. Lund and Manchester Groups. Clinical andneuropathological criteria for frontotemporal dementia. J NeurolNeurosurg Psychiat 1994; 57: 416–18.22. Neary D et al. Frontotemporal lobar degeneration. Neurology 1998;51: 1546–54.23. McKeith IG, Galasko D, Kosaka K, Perry E et al. Consensusguidelines for the clinical and pathologic diagnosis of dementia withLewy bodies (DLB). Neurology 1996; 47: 1113–24.24. Kopelman MD. The Korsakoff syndrome. Br J Psychiat 1995; 166:154–73.25. Collinge J. Human prion diseases: aetiology and clinical features. InGrowdon J, Rossor M, eds, Blue Books of Practical Neurology: TheDementias. Oxford: Butterworth-Heinemann, 1998; 113–48.26. McHugh P, Folstein M. Psychiatric syndromes of Huntington’schorea: a clinical and phenomenologic study. In Benson D, Blumer D,eds, Psychiatric Aspects of Neurologic Disease. New York: Grune andStratton, 1975; 267–85.

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