Adrenal Cortical Carcinoma: An Updated Review
نویسندگان
چکیده
This article reviews adrenal cortical carcinoma (ACC), especially associated synchronous and metachronous malignancies. The authors will discuss the genetic lesions associated with ACC, the clinical presentation, diagnosis, and treatment options. We hope to provide a thorough and updated review of this rare malignancy.
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گزارش بروز کارسینومای قشر فوق کلیه در 2 شیرخوار
Background: Adrenal cortical carcinoma is a rare malignant tumor which presents mainly in late adulthood with an equal age distribution. The tumor is usually functionally active. Case report: The present study reports two 11-month-old female infants with abdominal mass and virilysm who underwent radical nephrectomy. The final diagnosis was adrenal cortical carcinoma with regional lymph node...
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Adrenocortical carcinoma (ACC) is an uncommon malignancy originating from cortex of adrenal gland. The most common pitfall in diagnosis of ACC is to distinguish it from pheochromocytoma. Here we report a 62-year-old hypertensive man with presentation of dyspnea. The laboratory data showed an increase in urine cortisol and renin with a mild increase in aldosterone, but decrease in adrenocorticot...
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تاریخ انتشار 2018