Acta Neuropathologica

, Volume 112, Issue 1, pp 106–111

Ganglioglioma arising in a Peutz-Jeghers patient: a case report with molecular implications

Authors

    • Medical Genetics Unit, Department of Biomedicine of Evolutive AgeUniversity of Bari
  • Libero Lauriola
    • Deparment of PathologyCatholic University
  • Alfredo Puca
    • Institute of NeurosurgeryCatholic University
  • Francesco C. Susca
    • Medical Genetics Unit, Department of Biomedicine of Evolutive AgeUniversity of Bari
  • Alessio Albanese
    • Institute of NeurosurgeryCatholic University
  • Giovanni Sabatino
    • Institute of NeurosurgeryCatholic University
  • Marilena C. Di Giacomo
    • Medical Genetics Unit, Department of Biomedicine of Evolutive AgeUniversity of Bari
    • Deparment of PathologyCatholic University
    • Division of NeuropathologyNational Neurological Institute “C Besta”
  • Ginevra Guanti
    • Medical Genetics Unit, Department of Biomedicine of Evolutive AgeUniversity of Bari
Case Report

DOI: 10.1007/s00401-006-0084-6

Cite this article as:
Resta, N., Lauriola, L., Puca, A. et al. Acta Neuropathol (2006) 112: 106. doi:10.1007/s00401-006-0084-6

Abstract

The Peutz-Jeghers syndrome (PJS), an autosomal dominant disorder caused by inactivating germline mutations in the serine–threonine kinase gene LKB1, is characterized by mucocutaneous pigmentation, multiple gastrointestinal hamartomatous polyps, and by an increased risk for developing tumors involving several different organs. To date, no brain tumors have been described in PJS patients. In this report, we describe a case of ganglioglioma in a 22-year-old PJS patient. Single-strand conformation polymorphism-Heteroduplex analysis evidenced an abnormal pattern in exon 6 of the LKB1 gene. Sequencing revealed a 821delTinsAC mutation creating a termination codon 29 nucleotides downstream (p.Asn274fsX11). RNA studies showed an out-of-frame LKB1 isoform derived from the wild type allele and generated by exon 4 skipping. Since the LKB1 gene is expressed in the fetal and adult brain, our data would suggest its likely involvement in the pathogenesis of a subset of gangliogliomas.

Keywords

GangliogliomaPeutz-Jeghers syndromeLKB1SplicingExon skipping

Copyright information

© Springer-Verlag 2006