Triple gall bladder is a rare congenital anomaly. It was first reported separately in 1958 by Boni and by Skielboe. Since then only four further cases have appeared in the literature. An additional case demonstrated on routine oral cholecystography is described, together with a review of the literature.A 46-year-old male complaining of right hypochondrial pain was investigated by oral cholecystography. Physical examination was unremarkable.