The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma

D. G R Evans, L. A. Farndon, L. D. Burnell, H. Rao Gattamaneni, J. M. Birch

    Research output: Contribution to journalArticlepeer-review

    Abstract

    We have investigated the incidence of Gorlin syndrome (GS) in patients with the childhood brain tumour, medulloblastoma. One hundred and seventy-three consecutive cases of medulloblastoma in the North-West Regional Health Authority between 1954 and 1989 (Manchester Regional Health Board before 1974) were studied. After review of case notes, X rays and health surveys only 2/173 cases had evidence supporting a diagnosis of GS. A further case at 50% risk of GS died of a brain tumour aged 4 years. The incidence of GS in medulloblastoma is, therefore, probably between 1-2%. A population based study of GS in the region started in 1983 was used to assess the incidence of medulloblastoma in GS, which was found to be between 3-5%. This figure is lower than previous estimates, but this is the first population based study undertaken. In view of the early age of onset in GS (mean 2 years) children presenting with medulloblastoma, especially under 5 years, should be examined for signs of the syndrome. Those at high risk of developing multiple invasive basal cell carcinomata will then be identified.
    Original languageEnglish
    Pages (from-to)959-961
    Number of pages2
    JournalBritish Journal of Cancer
    Volume64
    Issue number5
    Publication statusPublished - 1991

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