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Congenital diverticula of the ventricles are rare and Skapinker (1951) was able to collect only twelve reported cases. In most of these, as in Skapinker's own patient, the diverticulum arose from the left ventricle but in two it communicated with both ventricles. Skapinker resected the diverticulum in his case, an operation that had previously been reported only once (Roessler, 1944); but further cases treated in this way have since been reported by Potts et al. (1953) and Bailey (1955). Other recent reports are by Formijne (1950), Snellen et al. (1952), and Parsons (1957). Included in the following description of a patient, in whom surgical resection was successfully undertaken, are electrocardiographic and manometric observations not hitherto recorded. The latter are possibly relevant to the mechanism of rupture of such diverticula, an accident known to have been the cause of death in at least three of the published cases.

CONGENITAL DIVERTICULUM OF THE LEFT VENTRICLE