Giant thoracolumbosacral teratoma in an infant

L Pollak1, J Schiffer, S Rochkind

  • 1Department of Neurosurgery, Assaf Harofeh Medical Center, 70300, Zerifin, Israel.

Insights

A rare sacrococcygeal teratoma with extensive spinal involvement was surgically removed in a 7-month-old infant. Postoperative recovery was successful with no neurological deficits observed.

Area of Science:

  • Pediatric Surgery
  • Developmental Biology
  • Oncology

Background:

  • Sacrococcygeal teratomas are congenital tumors, typically located at the tailbone.
  • Unusually high intraspinal extension of these tumors is rare and presents complex surgical challenges.

Purpose of the Study:

  • To report a rare case of sacrococcygeal teratoma with significant intraspinal extension.
  • To discuss the clinical presentation, surgical management, and outcomes of such cases.

Main Methods:

  • Case presentation of a 7-month-old male with a gluteal mass.
  • Diagnostic imaging using Magnetic Resonance Imaging (MRI) to delineate tumor extent.
  • Two-staged surgical resection of the tumor.
  • Histopathological examination for diagnosis.
  • Postoperative follow-up for neurological and functional recovery.

Main Results:

  • The tumor extended from the sacrococcygeal region up to the mid-thoracic spine.
  • Complete tumor removal was achieved in two stages.
  • Histology confirmed a benign teratoma.
  • Associated neurogenic bladder and constipation showed spontaneous improvement.
  • No neurological deficits were noted during a 3-year follow-up.

Conclusions:

  • Complete surgical resection is feasible for sacrococcygeal teratomas with high intraspinal extension.
  • Early diagnosis and surgical intervention can lead to favorable outcomes.
  • Benign teratomas, even with extensive involvement, may not result in permanent neurological damage.