Anyone can shoot me down for being wrong (I may be), but with a beta-keto acid, when you draw the mechanism, you form an enol first, which can tautomerize into a ketone (stable). With an alpha-keto acid, I don't think you form an enol. In fact, before releasing CO2, the intermediate is a carbocation that, on releasing CO2, pushes electrons onto the carbon which looks even less stable.