Abstract
CLOVES syndrome is a rare congenital disorder characterized by Congenital Lipomatous
Overgrowth of the trunk and/or thorax, Vascular malformations, skin abnormalities
(such as linear Epidermal nevi), and Skeletal anomalies, with scoliosis and tethered
cord being common features. This report presents the case of a 17-year-old boy with
clinical and imaging features consistent with CLOVES syndrome, confirmed by genetic
analysis demonstrating a somatic PIK3CA mutation.
Keywords
CLOVES - soft tissue overgrowth - vascular malformations