The natural history of subependymal giant cell astrocytomas in tuberous sclerosis complex: a review

Rev Neurosci. 2018 Mar 28;29(3):295-301. doi: 10.1515/revneuro-2017-0027.

Abstract

Tuberous sclerosis complex (TSC) is an auto-somal-dominant inherited condition with an incidence of approximately 1:6000 births, characterised by deregulated mTOR activity with multi-site hamartomas. Subependymal giant cell astrocytomas (SEGA) are one such hamartoma, affecting up to 24% of patients with TSC. Their intraventricular location may lead to life-threatening obstructive hydrocephalus. Current management is hampered by a lack of understanding regarding the natural history, behaviour and growth patterns of SEGA. We review the current literature to summarise what is known about SEGA in the following areas: (1) diagnostic criteria, (2) prevalence, (3) origin, (4) imaging characteristics, (5) growth rate, (6) genotype-phenotype correlation, (7) congenital SEGA and (8) SEGA as a marker of severity of other TSC manifestations.

Keywords: MRI; SEGA; TSC; genotype; growth; neuroimaging.

Publication types

  • Review

MeSH terms

  • Brain Neoplasms / complications*
  • Brain Neoplasms / diagnostic imaging
  • Brain Neoplasms / epidemiology*
  • Genetic Association Studies
  • Glioma, Subependymal / complications*
  • Glioma, Subependymal / diagnostic imaging
  • Glioma, Subependymal / epidemiology*
  • Humans
  • Neuroimaging
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism
  • Tuberous Sclerosis / complications*
  • Tuberous Sclerosis / diagnostic imaging
  • Tuberous Sclerosis / epidemiology*

Substances

  • MTOR protein, human
  • TOR Serine-Threonine Kinases