INCIDENTALLY DETECTED ADRENAL CORTICAL CARCINOMA

dc.creatorLy, Thu
dc.date.accessioned2022-07-05T15:05:18Z
dc.date.available2022-07-05T15:05:18Z
dc.date.issued2013-04-12
dc.description.abstractPurpose: Compared to benign adrenocortical tumors, adrenal cortical carcinomas (ACC) are rare occurrences affecting 1 out of 1,000,000 persons in the general population with a 3% prevalence rate in those older than 50 years old. Of interest is this unusual case of a nonfunctional adrenal cortical carcinoma in the left adrenal cortex in a 58-year old male. Methods: Laboratory evaluation was obtained while patient was in the hospital. This included plasma metanephrine, normetanephrine labs and a dexamethasone suppression test that ruled out pheochromocytoma and Cushing's syndrome. In addition, computerized tomography (CT) scan of the abdomen and pelvis was obtained. Results: The computerized tomography (CT) scan revealed a large, lobulated, heterogeneous density obliterating the left adrenal gland. Pathology reported adrenal cortical carcinoma from the biopsy. Conclusions: After surgical resection, further imaging was obtained that revealed metastasis into the lumbar spine. Oncology follow-up included mitotane chemotherapy.
dc.identifier.urihttps://hdl.handle.net/20.500.12503/31375
dc.subjectadrenal
dc.subjectadrenocortical
dc.subjectcarcinoma
dc.titleINCIDENTALLY DETECTED ADRENAL CORTICAL CARCINOMA
dc.typeposter
dc.type.materialtext

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