Adrenocortical carcinoma: Diagnosis & Treatments
Diagnosis Adrenocortical carcinoma is a rare cancer that occurs in one to two patients per million per year. Adrenocortical carcinoma is thought to be a very malignant tumor, but it exhibits very different biological and clinical characteristics for each individual. Patients with large, suspected adrenal tumors should be treated with a multidisciplinary team of medical professionals including endocrine, cancer, surgeon, radiologist, and pathologist. A suspected adrenocortical carcinoma is not an indication for FNA. First, malignancy and benignity of the adrenal mass can not be distinguished either cytologically or pathologically. Second, FNAs invade cancer capsules and can lead to cancer metastasis. It is difficult to distinguish benign from malignant pathologically even when the whole cancer mass is present. The most commonly used pathological category is Weiss Score. Weiss Score considers high nuclear grade, rate of dissection (> 5 / HPF), atypical cleavage, clear cell of 25% or ...