| Literature DB >> 32912887 |
Zahir S Hussain1, Smitha S Rao2, Wajith Z Hussain2, Shikhil Puzhakkal2.
Abstract
Adrenocortical carcinomas (ACCs) are rare malignancies with an incidence of one to two per million per year. Aldosterone-producing ACCs (APACs) are extremely rare with an incidence less than 1%. We describe a rare case of APAC, presenting with episodic lower-limb weakness and hypertension. Our patient was found to have serum aldosterone levels of 20.8 ng/dL (2.5-15.2) with persistent hypokalaemia and a 9.7×8.3×7.7 cm right adrenal mass, which was suspicious of malignancy on evaluation. He underwent a complete surgical resection which confirmed the diagnosis of ACC and normalised his aldosterone and potassium levels. He was then subjected to postoperative chemotherapy. Postoperative adjuvant chemotherapy with mitotane has a role in preventing recurrence. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: adrenal disorders; endocrine cancer; hypertension; surgical oncology; urological surgery
Mesh:
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Year: 2020 PMID: 32912887 PMCID: PMC7482498 DOI: 10.1136/bcr-2020-235317
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X