{Reference Type}: Case Reports
{Title}: Primary orbital rhabdoid tumour masquerading as atypical persistent foetal vasculature.
{Author}: Douch C;Merve A;Mankad K;Jorgensen M;
{Journal}: BMJ Case Rep
{Volume}: 17
{Issue}: 1
{Year}: 2024 Jan 9
暂无{DOI}: 10.1136/bcr-2022-250776
{Abstract}: We present a case of primary rhabdoid tumour of the orbit. Presenting features at birth included congenital ptosis, conjunctival injection, hyphaema and microphthalmia. The unique presentation caused a late diagnosis following the development of rapid proptosis 6 months later. We suggest that orbital rhabdoid tumour be considered in the differential diagnoses of patients presenting with atypical persistent foetal vasculature features.