# Diffuse glioma with FGFR3::TACC3 gene fusion and prominent calcification: A case report

## TL;DR

This case report describes a rare type of brain tumor with a specific gene fusion and unusual calcification patterns, offering insights into its radiological and genetic features.

## Contribution

The paper presents a rare case linking FGFR3::TACC3 fusion with prominent calcifications in a diffuse glioma.

## Key findings

- The tumor exhibited coarse and irregular calcifications visible on CT imaging.
- Genetic testing confirmed the presence of FGFR3::TACC3 fusion and FGFR3 amplification.
- MRI showed a diffuse growth pattern with infiltration across the corpus callosum.

## Abstract

Diffuse gliomas with fibroblast growth factor receptor 3 (FGFR3) and transforming acidic coiled-coil containing protein 3 (TACC3) gene fusion represent a distinct molecular subtype of isocitrate dehydrogenase (IDH)-wildtype gliomas characterized by unique histopathological features. Although microcalcifications have frequently been reported in histopathological studies, their prevalence and diagnostic significance on radiological imaging remain unclear. We report a case of a 67-year-old woman who presented with a 1-year history of weakness in the left lower limb. Head CT revealed coarse and irregular calcifications in the deep white matter of the right frontal and parietal lobes. At the same time, MRI demonstrated a diffuse gliomatosis cerebri-like growth pattern with infiltration across the corpus callosum and contrast enhancement in distant areas. Histopathological examination confirmed glioblastoma, IDH-wildtype, and subsequent genetic testing revealed FGFR3::TACC3 fusion and amplification of FGFR3 gene. This case highlights the potential radiological characteristics of diffuse gliomas with FGFR3::TACC3 fusion, particularly the presence of coarse calcifications, that may serve as notable imaging features of this tumor. Further research is required to determine whether calcification is a characteristic of this glioma subtype.