The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma

Br J Cancer. 1991 Nov;64(5):959-61. doi: 10.1038/bjc.1991.435.

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Basal Cell Nevus Syndrome / complications
  • Basal Cell Nevus Syndrome / epidemiology*
  • Basal Cell Nevus Syndrome / genetics
  • Cerebellar Neoplasms / complications
  • Cerebellar Neoplasms / epidemiology*
  • Cerebellar Neoplasms / genetics
  • Child
  • Child, Preschool
  • Family Health
  • Female
  • Humans
  • Incidence
  • Infant
  • Male
  • Medulloblastoma / complications
  • Medulloblastoma / epidemiology*
  • Medulloblastoma / genetics