Two patients with phaeochromocytomas developed crises in which severe hypertension alternated with profound hypotension.One patient died during a n emergency operation. T h e other was controlled with a long-acting alphacholinergic blocking agent and had his tumour removed uneventfully.PATIENTS with phaeochromocytomas may develop paroxysmal attacks of hypertension (Labbe, Tinel, and Doumer, 1922). Although a n almost rhythmical 2.5 0.25 PHENTOLAMl M Lv.(mg)$ $ NORADRENALINE DRIP mwere available. T h e second patient responded satisfactorily to phenoxybenzamine, and subsequent removal of the tumour was straightforward.
CASE REPORTSCase I.-A 57-year-old farmer was admitted to the Royal Victoria Hospital, Belfast, on, 6 Feb., 1962, for investigation of headaches, excessive sweating, and irritability, which he had had for 3 months. He was rather obese, but the only other abnormal findings were a blood-pressure of 13o/11o mm. Hg and a coarse tremor in both hands. His haemoglobin level was 14.9 g. per ~o o m l . and there was a slight leucocytosis of 13,700 per cu. mm. with a normal differential count. Glycosuria 0.25 0.25 0.1 0.1 0.1 TO THEATRE J -1 J. J. J.