Leukemia Research Reports (Jan 2024)

A rare association of a high grade glioblastoma, cerebral abscess and acute lymphoblastic leukemia in a child with Noonan syndrome

  • Wiem Boufrikha,
  • Rim Rakez,
  • Inaam Bizid,
  • M.Maher Hadhri,
  • Manel Njima,
  • Sarra Boukhris,
  • M.Adnene Laatiri

Journal volume & issue
Vol. 21
p. 100404

Abstract

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Noonan syndrome is a genetic disorder frequently caused by PTPN11 mutations. Patients with Noonan syndrome are characterized by facial dysmorphism, short stature and congenital heart defects and they have a reported predisposition to malignancies such as leukemia, and solid and central nervous system tumors. Here, we report a case of a 14-year-old boy with Noonan syndrome treated for T-cell acute lymphoblastic leukemia who presented with 2 concomitant abnormalities: cerebral abscess and high grade glioblastoma. This exceptional association exhibits to a poorer prognosis and may sometimes delay the diagnosis and therefore the therapeutic intervention.

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