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. Author manuscript; available in PMC: 2021 Jan 5.
Published in final edited form as: J Neurosurg Spine. 2019 Jul 5;31(4):607–615. doi: 10.3171/2019.4.SPINE19178

TABLE 1.

Demographic and clinical characteristics of the study cohort

Variable Value
No. of patients 38
Mean age, yrs 8.0 ± 7.2
Sex
 Female 26 (68.4)
 Male 12 (31.6)
Lesion pathology
 Ependymoma 3 (7.9)
 Pilocytic astrocytoma 5 (13.2)
 Pilomyxoid astrocytoma 1 (2.6)
 Diffuse astrocytoma 1 (2.6)
 Glioblastoma 1 (2.6)
 Medulloblastoma 9 (23.7)
 Schwannoma 2 (5.3)
 Ganglioglioma 2 (5.3)
 ATRT 2 (5.3)
 Germinoma 2 (5.3)
 PNET 2 (5.3)
 Neuroblastoma 2 (5.3)
 Other* 6 (15.8)
Primary site of disease
 Cerebrum 4 (10.5)
 Posterior fossa 14 (36.8)
 Spine vertebrae 3 (7.9)
 Spinal cord 12 (31.6)
 Other 5 (13.2)

ATRT = atypical teratoid rhabdoid tumor; PNET = primitive neuroectodermal tumor.

Values are expressed as mean ± standard deviation or number of patients (%).

*

Other lesion pathologies include optic pathway glioma, neuroblastoma, neurocutaneous melanosis, choroid plexus carcinoma, meningioma, pineoblastoma, and benign lymphovascular lesion.

Other sites include optic chasm, lateral ventricle, pituitary stalk, and pineal gland.