“…The patient had a typical clinical picture of phaeochromocytoma with episodes of rising blood pressure and increased catecholamine excretion. It was previously held that a malignant phaeochromocytoma is unable to increase pressure (McGavack, Benjamin, Speer and Klotz, 1942;Washington, Callahan and Edwards, 1946), but later observations have shown that both the primary tumour (Brines andJennings, 1948 Kimberley, 1956;Scheinin, 1960) and metastases (Davis et al, 1955;Bjorck, Linderholm, Lublin, Pernow and Tornberg, 1959;Kennedy, Symington and Woodger, 1961) can be pharmacologically active. Palmieri et al (1961) have even been inclined to refuse the classification malignant to phaeochromocytomas without clinical signs.…”