Novel paediatric case of a spinal high-grade astrocytoma with piloid features in a patient with Noonan Syndrome
Year: 2024
Type: article
Study design: Case Report
Abstract: Noonan Syndrome (NS) is associated with an increased risk of low-grade central nervous system tumours in children but only very rarely associated with high-grade gliomas. Here we describe the first reported case of a spinal high-grade astrocytoma with piloid features (HGAP) in a child with NS. This case was a diagnostic and treatment dilemma, prior to whole-genome germline and tumour sequencing, tumour transcriptome sequencing and DNA methylation analysis. The methylation profile matched strongly with HGAP and sequencing identified somatic FGFR1 and NF1 variants and a PTPN11 germline pathogenic variant. Therapeutic targets were identified but also alterations novel to HGAP such as differential expression of VEGFA and PD-L1. The germline PTPN11 finding has not been previously described in individuals with HGAP. This case underscores the power of precision medicine from a diagnostic, therapeutic and clinical management perspective, and describes an association between HGAP and NS which has not previously been reported.
Source: npj Precision Oncology
Language: English
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,790
Funders: Children's Hospital Foundation, Australian Government, Australian Cancer Research Foundation, Cancer Australia, Cancer Institute NSW, University of New South Wales, Cure Brain Cancer Foundation, NSW Ministry of Health, Minderoo Foundation, Australian Genomics Health Alliance, Kids Cancer Alliance, Tour de Cure, Medical Research Council, National Health and Medical Research Council
OpenAlex ID: W4403562327
