A RARE CASE OF ADRENOCORTICAL CARCINOMA: A CASE REPORT
Abstract
Adrenocortical carcinoma (ACC) is a rare, heterogeneous malignancy with a poor prognosis. ACCs may
be hormone functioning and non-functioning , sign and symptoms develop depending upon the excessive
hormone secreted. Surgical resection is the preferred treatment option . Presenting a 60 year old male patient with complaints of
abdominal pain , weight loss , hypertension and hyperglycemia diagnosed as malignancy in adrenal gland in CECT abdomen ,
operated for right open adrenalectomy. Histopathological examination suggestive of : adrenocortical carcinoma
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PDFReferences
Sabiston textbook of surgery 1st south Asian edition
Bailey and Love short practice of surgery 27th edition
Smith and Tanagho’s general urology , 19th edition
Campbell-Walsh urology , 11th edition
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