Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-25T13:50:00.634Z Has data issue: false hasContentIssue false
  • English
  • Français

Psychiatric Vulnerability and Cerebellar Haemangioblastoma

A Case Report

Published online by Cambridge University Press:  02 January 2018

D. A. Summerfield
D. A. Summerfield*
Affiliation:
St George's Hospital, Tooting, London SW17 0RE
Get access Rights & Permissions [Opens in a new window]

Abstract

A case of cerebellar haemangioblastoma in described in a middle-aged woman with a history of multiple psychiatric admissions for depressive and psychosomatic symptomatology. The diagnosis was not made until a late stage, largely because of the knowledge of her psychiatric history and its particular slant. Similar psychiatric symptoms were present at the outset, colouring the emerging neurological picture. The clinical manifestations and management of cerebellar haemangioblastoma are described.

Type
Brief Reports
Information
The British Journal of Psychiatry , Volume 150 , Issue 6 , June 1987 , pp. 858 - 860
Copyright
Copyright © 1987 The Royal College of Psychiatrists 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Hecaen, H. & Ajuriaguerra, J. (1956) Mental Disturbances in Intracranial Tumours. Paris: Masson.Google Scholar
Horton, W., Wong, V. & Eldridge, R. (1976) Von Hippel Lindau's disease: clinical and pathological manifestations in families with 50 affected members. Archives of Internal Medicine, 136, 769–777.CrossRefGoogle Scholar
Lindau, A. (1931) Vascular tumours of brain and spinal cord. Proceedings of the Royal Society of Medicine, 24, 363.Google Scholar
Merskey, H. (1986) The importance of hysteria. British Journal of Psychiatry, 149, 23–27.Google Scholar
Mohan, J., Brownell, B. B. & Oppenheimer, D. (1976) Malignant spread of haemangioblastoma – 2 cases. Journal of Neurology, Neurosurgery and Psychiatry, 39, 515.Google Scholar
Morello, G. & Blanch, I. M. (1963) Cerebellar haemangioblastoma. Journal of Neurosurgery, 20, 254.Google Scholar
Nibbelink, D., Peters, B. & McCormick, W. (1969) Association of phaeochromocytoma and cerebellar haemangioblastoma. Neurology, 19, 455–460.CrossRefGoogle Scholar
Nicol, A. (1957) Lindau's disease in five generations. Annals of Human Genetics, 22, 7.Google Scholar
Olivecrona, H. (1952) Cerebellar angioreticulomas. Journal of Neurosurgery, 9, 317.CrossRefGoogle ScholarPubMed
Palmer, J. (1972) Review of 81 cases of haemangioblastoma. Acta Neurochirurgica, 27, 125–148.Google Scholar
Slater, E. (1965) Diagnosis of hysteria. British Medical Journal, 1, 1395–1399.Google Scholar
Waldmann, J., Levin, E. & Baldwin, M. (1961) The association of polycythaemia with cerebellar haemangioblastoma. American Journal of Medicine, 31, 318–324.Google Scholar
Yamashita, J., Handa, H., Kim, C. & Kim, S. (1982) Familial occurrence of cerebellar haemangioblastoma – analysis of five families. Neurosurgery, 11, 761–763.Google Scholar
Submit a response

eLetters

No eLetters have been published for this article.