Relapse and metastasis of atypical teratoid/rhabdoid tumor in a boy with neurofibromatosis type 1 treated with recombinant human growth hormone

Neuropediatrics. 2015 Apr;46(2):126-9. doi: 10.1055/s-0034-1393706. Epub 2015 Jan 27.

Abstract

Even though no increased recurrence rate seems to be reported in patients with brain tumors receiving recombinant human growth hormone (rhGH) replacement, in some patients multiple risk factors could put at higher risk for recurrence. In such cases, the decision to start rhGH therapy should be very cautious. A boy with neurofibromatosis type 1 developed an atypical teratoid/rhabdoid tumor (AT/RT) of right cerebellum, treated with surgery, radiotherapy, and chemotherapy. After 3 years of remission, he started rhGH for growth hormone deficiency, having a negative magnetic resonance imaging (MRI) scan. Ten weeks after starting therapy, the boy became symptomatic and MRI showed relapse of AT/RT in the right cerebellum and a new lesion in the brainstem. The boy died of progressive disease. In this case, the connection between AT/RT recurrence and the beginning of rhGH therapy, with a negative pretreatment MRI, cannot be excluded. Additional caution should be used for rhGH in patients with multiple risk factors.

Publication types

  • Case Reports

MeSH terms

  • Brain Stem Neoplasms / pathology
  • Brain Stem Neoplasms / secondary*
  • Cerebellar Neoplasms / drug therapy*
  • Cerebellar Neoplasms / pathology
  • Child
  • Human Growth Hormone / adverse effects*
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Neurofibromatosis 1 / drug therapy*
  • Neurofibromatosis 1 / pathology
  • Recombinant Proteins / adverse effects
  • Recurrence
  • Rhabdoid Tumor / drug therapy*
  • Rhabdoid Tumor / pathology
  • Risk Factors
  • Teratoma / drug therapy*
  • Teratoma / pathology

Substances

  • Recombinant Proteins
  • Human Growth Hormone

Supplementary concepts

  • Teratoid Tumor, Atypical