Spinal Peripheral Primitive Neuroectodermal Tumors: A Radiological Analysis of Ten Cases

Turk Neurosurg. 2019;29(1):33-42. doi: 10.5137/1019-5149.JTN.21931-17.2.

Abstract

Aim: To summarize the imaging features of spinal peripheral primitive neuroectodermal tumor (spPNET) patients.

Material and methods: The computed tomography and magnetic resonance imaging features of 10 spPNET patients, four men and six women, were retrospectively analyzed, and their clinicopathological data were reviewed.

Results: The mean age of the patients was 24.7 years (range, 3-44 years). Ten spPNET lesions were found in the ten patients, including six extradural and four intradural extramedullary lesions. Radiologically, spPNET typically presented as heterogeneous isointense lesions with a heterogeneously enhanced pattern. A "vault wall-like growth" pattern, a linear enhancement pattern, and vertebral bone involvement tended to be found in the extradural lesions, whereas a ring enhancement pattern was found in the extramedullary intradural lesions. Positive Ki-67 expression might be related to necrosis, bone destruction, and hemorrhage.

Conclusion: A well-defined spinal mass showing isointensity/attenuation with heterogeneous enhancement accompanied by other imaging features may be suggestive of spPNET and should be added to the list of differential diagnosis.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Magnetic Resonance Imaging / methods
  • Male
  • Neuroectodermal Tumors, Primitive, Peripheral / diagnostic imaging
  • Neuroectodermal Tumors, Primitive, Peripheral / pathology*
  • Retrospective Studies
  • Spinal Cord Neoplasms / diagnostic imaging
  • Spinal Cord Neoplasms / pathology*
  • Tomography, X-Ray Computed / methods
  • Young Adult