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← Childhood Cancer Genomics (PDQ®)

HEALTH PROFESSIONAL · SOURCE READING

Spinal ependymoma with MYCN amplification (SP-EPN-MYCN)

Source: Childhood Cancer Genomics (PDQ®)–Health Professional Version, National Cancer Institute.

Source updated: April 30, 2025 · Captured 2026-09-09.

Selected source text with whitespace normalised. This Triangle page is not an NCI PDQ summary. Independent clinical review is pending.

Context: Central Nervous System Tumors / Ependymomas / Molecular Subgroups of Ependymoma

SP-EPN-MYCN is rare, with only 27 cases reported.[188-191]

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Median age at presentation was 31 years (range, 12–56 years).

High level of MYCN amplification was present at diagnosis and relapse.

SP-EPN-MYCN has a unique methylation profile compared with other spinal cord ependymomas, MYCN-amplified pediatric-type glioblastoma, and neuroblastoma.

For information about the treatment of childhood ependymoma, see Childhood Ependymoma Treatment.

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Preserved source evidence · Independent clinical review pending · Not medical advice