Skip to main content
Fig. 1 | Clinical Epigenetics

Fig. 1

From: Supratentorial CNS-PNETs in children; a Swedish population-based study with molecular re-evaluation and long-term follow-up

Fig. 1

Cohort overview. A. Distribution of tumour types after histopathological and molecular re-evaluation of 71 supratentorial CNS-PNETs; B and C. Further subdivision of the tumour types based on the histopathological re-evaluation; HGGs (n = 25) and OTHER diagnoses (n = 14) Abbreviations: HGG, high-grade glioma; AT/RT, atypical teratoid/rhabdoid tumour; CNS NB-FOXR2, CNS neuroblastoma, FOXR2-activated; ETMR, embryonal tumour with multilayered rosettes; EPN, ependymoma; DHG, H3 G34-mutant, diffuse hemispheric glioma H3 G34-mutant; DMG, K27, diffuse midline glioma H3 K27-altered; IHG, infant-type hemispheric glioma; HGG NOS, high-grade glioma not otherwise specified; PBL, pineoblastoma; CPC, choroid plexus carcinoma

Back to article page

Clinical Epigenetics

ISSN: 1868-7083

Contact us