AI Article Synopsis

  • A 3-year-old girl presented with a growing mass in her neck that she had since birth; imaging revealed issues with the spinal canal and a fatty tumor.
  • Surgical removal of the tumor confirmed it was a mature teratoma, a rare type of tumor in pediatric patients.
  • The study included a review of six additional cases to provide more information on spinal teratomas, noting that most patients underwent surgery, with one receiving chemotherapy and radiation.

Article Abstract

Here, we report a case of a 3-year-old female who presented to clinic with an enlarging mass in the posterior cervical midline. The mass was present since birth and demonstrated no cutaneous stigmata. Plain film, CT, and MRI of the cervical spine (C3-C5) revealed enlargement of the spinal canal, soft tissue calcification, spinal dysraphism, and an intramedullary, predominantly fatty, mass. The mass had associated calcifications and a highly proteinaceous cyst. Surgical resection of the spinal lesion was subsequently performed. Histopathological evaluation revealed a mature teratoma. Cervical spinal teratomas in the pediatric population are rare entities with few cases currently reported in the literature. We conducted a systematic review to outline the current evidence detailing cases of intramedullary spinal cord teratomas. Six articles were included for final review. All patients in the included articles underwent maximal surgical resection with one patient also receiving chemotherapy and radiation. With our report, we aim to add to the literature on cervical intramedullary spinal cord teratomas in the pediatric population.

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Source
http://dx.doi.org/10.1007/s00381-021-05385-4DOI Listing

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