International Journal of Geriatric Psychiatry Volume 20 Issue 1 2005 [Doi 10.1002%2Fgps.1220] P. J. Connelly; C. Rodriguez-Castello; L. M. Robertson -- Odysseus Syndrome- Nihilism

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  • 8/10/2019 International Journal of Geriatric Psychiatry Volume 20 Issue 1 2005 [Doi 10.1002%2Fgps.1220] P. J. Connelly; C.

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    INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY

    Int J Geriatr Psychiatry2005; 20: 8384.

    Published online in Wiley InterScience (www.interscience.wiley.com). DOI: 10.1002/gps.1220

    RESEARCH LETTER

    Odysseus syndrome: nihilism by proxy

    P. J. Connelly*, C. Rodriguez-Castello and L. M. Robertson

    Murray Royal Hospital, Perth, Scotland

    INTRODUCTION

    Onset of Cotards syndrome after age 70 is uncom-mon (Berrios and Luque, 1995), but older peopleare more likely to have hypochondriacal delusions,

    delusions of non-existence and of immortality, rarelywith a feeling of enormity of the body (Berrios andLuque, 1995). To our knowledge, no cases have beenreported in which the patient believed firmly thatwhilst they were personally unaffected, relatives hadsuffered significant degenerative change or hadindeed died despite clear evidence to the contrary.

    CASE 1

    An 81-year-old lady presented to psychiatric servicesfor the first time with sudden onset of ideas that hergrandson had developed grossly swollen legs, inflam-

    mation of the brain, lethargy and extreme tirednessafter infection by a fly which had picked up radioac-tive waste in the English Channel. Despite speaking tohim over the telephone, she believed that he had died.She believed that he had no stomach or internalorgans, that his eyes had been removed and replacedwith glass eyes, that his brain had died and beenreplaced by a clock and that he had expanded tobecome grossly obese. She described hallucinationsof police providing commentary on his actions, butno other first rank symptoms of schizophrenia. Hermood was subjectively depressed but this clearlypost-dated the onset of her delusions. Vegetative

    symptomatology, including psychomotor retardationand agitation, were absent. Mini Mental State Exam-

    ination (MMSE) score was 27/30 and verbal fluencywas reduced. Her only physical problem was well-controlled atrial fibrillation. Haematology, biochem-istry, serology and CT brain scan were normal. Onesister had a long term diagnosis of schizophrenia.

    Over the next five years these delusions remainedvirtually unchanged. She was very intolerant of anti-psychotic medication including clozapine. Sherefused to consider ECT. Two years after initial pre-sentation, she had a brief depressive episode whichresponded to Lofepramine, though this did not alterher delusions. Currently, she continues to harbourthese mood-incongruent beliefs but functions reason-ably independently within a residential home, with acurrent MMSE of 18/30.

    CASE 2

    A 73-year-old lady with a 40 year history of paranoidschizophrenia presented with grossly elated mood,over-activity, over-talkativeness, distractibility andgrandiose beliefs. She sought help to prevent experi-mentation on her lovers health in the flat next door.

    She maintained he had developed The Pox lead-ing to his limbs rotting away, his heart being replacedby a machine and his brain requiring removal. Shebelieved nonetheless that he could send messages toher via television to which she could respond byarranging candles in a certain fashion. She wasobserved to be hallucinating to his voice. She main-tained that he had died but come back to live in her

    mattress in a grossly distorted form, being very muchlarger than he had been in real life.

    Her mood stabilised on a combination of Lithiumand Sodium Valproate. Conventional and atypicalantipsychotics including clozapine all proved ineffec-tive in changing the intensity or content of her delu-sions, which remained mood-incongruent over five

    Received 24 May 2004Copyright# 2004 John Wiley & Sons, Ltd. Accepted 12 August 2004

    *Correspondence to: Dr P. J. Connelly, Murray Royal Hospital,Muirhall Road, Perth, PH2 7BH, UK. Tel: 01738 562335. Fax:01738 440431. E-mail: [email protected]

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    years. Initially MMSE was 30/30, but recently hasdeclined to 13/30.

    DISCUSSION

    Our two cases meet diagnostic criteria for schizophre-nia, albeit with an affective element, though variation

    in prevailing mood made no difference to the intensityor content of the delusional ideation. Case 2 sufferedfrom partition delusions a characteristic of late lifeparanoid schizophrenia (Herbert and Jacobsen, 1967).Cognitive deterioration on long-term follow-up ofsimilar patients is common (Hymas et al., 1989) asis chronicity of delusions (Hymas et al., 1989)although Enoch and Trethowan (1991) report that epi-sodes of Cotards syndrome are usually short-lived.Strikingly, in the series of Berrios and Luque(1995), none of the 100 patients had any delusionwhich is comparable to those reported in our twocases.

    In both our cases, patients express nihilistic feel-ings of decay and death of bodily organs or the personas a whole, despite evidence to the contrary, withenormity of the body and immortality of the sufferer,

    who was able to function despite having died. Ifexpressed in relation to themselves, a diagnosis ofCotards syndrome would be appropriate. We believeit is reasonable to consider these patients as showingevidence of nihilism by proxy and we suggest thename Odysseus syndrome for this delusion.

    In Homers Odyssey, Odysseus was a hero in the

    Greco-Trojan War who took many years to returnhome. His wife Penelope believed him dead. On hiseventual return, the Goddess Athene made him looktaller and stronger so that he took on the appearanceof an immortal. Then he was presented to his wifewho continued to believe him dead for a time despiteevidence to the contrary.

    REFERENCES

    Berrios GE, Luque R. 1995. Cotards syndrome: analysis of 100cases. Acta Psychiatr Scand91: 185188.

    Enoch D, Trethowan W. 1991. Cotards Syndrome. In UncommonPsychiatric Syndromes, 3rd edn. Butterworth-Heinemann:

    Oxford; 162183.Herbert ME, Jacobson S. 1967. Late Paraphrenia. Br J Psychiatry

    113: 461469.Hymas N, Naguib M, Levy R. 1989. Late paraphreniaa follow-

    up study. Int J Geriatr Psychiatry 4: 2329.

    84 p. j. connelly ET AL.

    Copyright# 2004 John Wiley & Sons, Ltd. Int J Geriatr Psychiatry2005; 20: 8384.