“…Recurrences and metastases frequently evolve within 2 years of diagnosis and death occurs either by local tumor extension or by development of lymph node, lung, liver or spleen metastases. The first report of an adrenal angiosarcoma was published in 1967 [16], and clinical and pathological characteristics of the 21 patients who have been reported so far are shown in table 1 [16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29]. Of interest, adrenal function was normal in all patients in whom it was evaluated (patients 4, 7, 12–21).…”