Abstract:Background Adenomatoid tumours are presented as rare neoplasms of mesothelian origin, with different location, which can easily mimic specific diseases presented as adrenal incidantelomas, eg pheochromytoma, Cushing syndrome or adrenal carcinoma. The incidence does not allow providing specific pathognomic characteristics and the differential diagnosis may be proven challenging. Case presentation NK, a 49 year old mechanic engineer, without remarkable medical history, non smoker, was examined by cardiologist (I… Show more
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