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AimsWe describe three cases of primary adrenocortical carcinoma (ACC) with prominent rhabdoid features and study their clinicopathological and immunohistochemical properties.
Methods and resultsThe patients were three females aged 45–55 years (mean 49 years), none of whom had any hormone‐related symptoms. Histologically, the characteristic features were rhabdoid tumour cells with prominent eosinophilic...
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