Sacrococcygeal teratoma with intraspinal extension: A case series and review of literature.

J Pediatr Surg

Great Ormond Street Hospital for Children, Department of Paediatric Surgery-Specialist Neonatal and Paediatric Surgery, NHS Foundation Trust, Great Ormond Street, London WC1N 3JH. Electronic address:

Published: October 2020

AI Article Synopsis

  • Sacrococcygeal teratoma (SCT) is the most common type of teratoma in newborns and rarely extends into the spinal canal, with only a few cases reported.
  • A study at one institution found three patients with SCT and intraspinal invasion, highlighting the importance of MRI for accurate diagnosis and surgical planning, and recommending a multidisciplinary team approach for management.
  • Early diagnosis and exclusion of intraspinal extension are crucial for successful treatment, emphasizing the need for MRI if ultrasound suggests spinal invasion prior to surgery.

Article Abstract

Background: Sacrococcygeal teratoma (SCT) is the most common teratoma in neonates and arises from the coccyx. SCT with intraspinal invasion is extremely rare and only reported in a few cases.

Methods: 37 patients with SCT were identified at our institution between 2000 and 2018. Three of these patients had SCT with intraspinal extension. A literature review for intraspinal extension associated with SCT, including mode of diagnosis, presentation, surgical approach and neurological sequelae, between 1993 and 2018 was also conducted.

Results: The authors report three cases of infants who were antenatally and/or postnatally diagnosed with a sacrococcygeal teratoma extending into the spinal canal. We illustrate the challenges of accurate diagnosis and therapeutic management. Postnatal magnet resonance imaging (MRI) was the best method to define spinal anatomy and extension of the tumors prior to surgery. Management with a multidisciplinary team approach including neuroradiology, neurosurgery and general surgery was used in our two most recent patients. The literature review yielded 6 cases of SCT with intraspinal extension.

Conclusion: Intraspinal extension in SCT is rare but should be excluded at birth before attempting any resection. In case of positive spinal invasion on Ultrasonography (US), MRI is essential to plan for surgery and possible laminectomy to be able to perform a radical resection of this congenital tumor. We recommend this multidisciplinary approach.

Level Of Evidence: Level IV.

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Source
http://dx.doi.org/10.1016/j.jpedsurg.2020.02.003DOI Listing

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