Solitary fibrous tumours (SFTs) are soft tissue tumours of fibroblastic origin. 1 These tumours were first reported in pleura but are also detected at extra-pleural locations. 2,3 The underlying genetic pathology is a paracentric inversion in chromosome 12q, leading to NAB2-STAT6 gene fusion, which further activates several growth factor pathways. 1,2,4 Morphologically, these tumours are composed of spindle-shaped cells along with prominent, dilated and branching blood vessels, described as "staghorn vasculature". 5