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Parkinsonism — Dementia Complex, Hydrocephalus and Paget’s Disease

Published online by Cambridge University Press:  15 November 2018

M. I. Botez ,
Gilles Bertrand ,
Jean Léveillé  and
Luc Marchand
M. I. Botez*
Affiliation:
Hôtel-Dieu Hospital, Neurosurgical Service of Montreal Neurological Hospital and , Clinical Research Institute of Montreal, Montreal, Canada
Gilles Bertrand
Affiliation:
Hôtel-Dieu Hospital, Neurosurgical Service of Montreal Neurological Hospital and , Clinical Research Institute of Montreal, Montreal, Canada
Jean Léveillé
Affiliation:
Hôtel-Dieu Hospital, Neurosurgical Service of Montreal Neurological Hospital and , Clinical Research Institute of Montreal, Montreal, Canada
Luc Marchand
Affiliation:
Hôtel-Dieu Hospital, Neurosurgical Service of Montreal Neurological Hospital and , Clinical Research Institute of Montreal, Montreal, Canada
*
Clinical Research Institute of Montreal, 110 Pine Avenue West, Montreal, Que., H2W 1R7 Canada
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Summary

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A 65-year-old female patient with Paget’s disease displayed dementia, a bilateral Parkinsonian syndrome, gait ataxia, bilateral grasp reflex of the feet, urinary incontinence and a left hemicerebellar syndrome. She had a marked basilar impression; the radionuclide cisterno gram was suggestive of a communicating hydrocephalus with ventricular dilatation. After a shunting procedure there was improvement in both neurological and mental function.

Résumé

Résumé

Les auteurs présentent l’observation clinique d’une patiente âgée de 65 ans qui avait une maladie de Paget avec démence, syndrome Parkinsonien bilatéral, ataxie de la marche, réflexe de préhension des pieds, incontinence urinaire et un hémisyndrome cérébelleux gauche. La radiographie du crâne a montré une invagination basilaire; la scintycisternographie avec III. In a mis en évidence une hydrocéphalie communicante. On a pratiqué une dérivation ventriculo-atriale qui a amené une amélioration autant du point de vue neurologique que du point de vue psychique.

Type
Research Article
Information
Canadian Journal of Neurological Sciences , Volume 4 , Issue 2 , May 1977 , pp. 139 - 142
Copyright
Copyright © Canadian Neurological Sciences Federation 1977

References

Adams, R. D., Fisher, C. M., Hakim, S., Ojemann, B. G. and Sweet, W. H. (1965). Symptomatic occult hydrocephalus with normal cerebrospinal fluid. A treatable syndrome. New England Journal of Medicine, 273, 117–130.Google Scholar
Botez, M. I. (1974). Frontal lobe tumours. In Handbook of Clinical Neurology, vol. 17 p. 249. Edited by Vinken, P. J. and Bruyn, G. W.. North-Holland Publ. Co., Amsterdam.Google Scholar
Botez, M. I. (1976). The placing reaction in adult neurology. Canadian Journal of Neurological Sciences, 3, 189–198.Google Scholar
Botez, M. I., Ethier, R., Léveillé, J. and Thérèse, Botez. (1976). A syndrome of early recognition of occult hydrocephalus and cerebral atrophy. Quarterly Journal of Medicine, New Series, 181, 815–830.Google Scholar
Botez, M. I., Léveillé, J., Bérubé, L. and Botez-Marquard, T (1975). Occult disorders of the cerebrospinal fluid dynamics. European Neurology, 13, 203–223.Google Scholar
Botez, M. I., Léveillé, J., Marchand, L., Beroniade, V, Marquard-Botez, Th. and Bérubé, L. (1974). Le dépistage clinique, neuropsychologique et radioisotopique précoce de l’hydrocéphalie occulte et des atrophies cérébrales chez l’adulte. Union médicale du Canada, 103, 1032–1050.Google Scholar
Boudin, G., Le Besnerais, Y., Godlewski, S. and Fabiani, J. M. (1975). Les complications neurologiques des impressions basilaires pagétiques et leur traitement chirurgical. Semaine des Hôpitaux, Paris, 51, 145–155.Google Scholar
Clegg, J. L. (1937). Page’s disease with mental symptoms and choroiditis. Lancet, 2, 128–131.Google Scholar
Culebras, A., Feldman, R. G. and Fager, C. A. (1974). Hydrocephalus and dementia in Page’s disease of the skull. Journal of Neurological Sciences, 23, 307–321.CrossRefGoogle Scholar
Dimitri, V. and Aronovitch, J. (1936). Alteractiones encefalicos en uno caso de enfermedad de Paget, Revista di Neurologia, (Buenos Aires) 1, 139–151.Google Scholar
Fradis, A. and Botez, M. I. (1958). The groping phenomena of the foot. Brain, 81, 218–230.Google Scholar
Goldstein, K. (1938). The tonic foot response to stimulation of the sole; its physiological significance and diagnostic value. Brain, 61, 269–283.CrossRefGoogle Scholar
Goodbody, R. A. and Roberts, L. V. (1950). Basilar invagination in Page’s disease. Lancet, 1, 809–811.Google Scholar
Grossiord, A., Lacert, P. H., Pannier, S., Bedoiseau, M. and Tancrede, C. (1667). Impression basilaire et maladie de Paget. Revue neurologique, 116, 250–258.Google Scholar
Hann, R. C. (1910). A case of osteitis deformans terminating with cerebral symptoms. British Medical Journal, 1, 135–137.Google Scholar
Katzenststein-Sutro, E. and Bosch-Gwalter, T. (1960). Neurologische und psychiatrische Symptomatologie in Gesamtbild der Osteitis deformans Paget. Schweizerische Archi w für Neurologie, Neurochirurgie und Psychiatrie, 85, 11–61.Google Scholar
Messert, B. and Wannamacker, B. B. (1974). Reappraisal of the occult hydrocephalus syndrome. Neurology (Minneap.), 24, 224–231.Google Scholar
Moynan, R. S. (1928). Osteitis deformane with psychosis. Report of a case. Ohio State Medical Journal, 24, 206–209.Google Scholar
Noica, D. and Draganesco, S. (1935). Sur un symptôme caractéristique d’une lésion des noyaux centraux moteurs. La rigidité musculaire latente. Revue neurologique, 63, 75–79.Google Scholar
Riser, M., Gayral, G., Lazorthes, G. and Hivert, M. (1948). Etat mélancolique grave au cours d’une maladie osseuse de Paget à localisation crânienne exclusive. Annales medico-psychologiques, 2, 69–73.Google Scholar
Schuster, P. and Pineas, H. (1926). Weitere Beobachtungen über Zwangsgreifen und Nachgreifen und deren Beziehungen zu ähnlichen Bewegungstorungen. Deutsche Zeitschrift für Nervenheilkunde, 26, 29–42.Google Scholar
Stauder, K. H. (1933). Psychische Störungen bei Osteitis deformans (Paget) des Schädels. Archiw für Psychiatrie und Nervenkrankheiten, 98, 546–566.CrossRefGoogle Scholar
Sypert, G. W. Leffman, H. and Ojemann, G. A. (1973). Occult normal pressure hydrocephalus manifested by Parkinsonism-dementia complex. Neurollogy (Minneap.) 23, 234–238.Google Scholar