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Abstract. Background and aims: Adrenocortical carcinoma (ACC) is a rare tumour with an incidence of approximately 0.52 cases per million per year. Diagnosis is mostly delayed and prognosis is poor. We report our experiences with 11 patients operated on within the last 10 years. Patients/Methods: The data of the patients with ACC were reviewed and presenting symptoms, diagnostic procedures, treatment...
. Background and aims: Adrenocortical carcinoma (ACC) is a rare tumour with an incidence of approximately 0.5–2 cases per million per year. Diagnosis is mostly delayed and prognosis is poor. We report our experiences with 11 patients operated on within the last 10 years. Patients/Methods: The data of the patients with ACC were reviewed and presenting symptoms, diagnostic procedures, treatment and...
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