A Case Report of Bilateral Adrenocortical Carcinoma Complicated by Adrenal Insufficiency.
10.3803/EnM.2011.26.3.243
- Author:
Min Joo KIM
1
;
Jung Hee KIM
;
Tae Young KIM
;
Sang Wan KIM
Author Information
1. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
- Publication Type:Case Report
- Keywords:
Adrenal cortex neoplasm;
Adrenal insufficiency;
Adrenocortical carcinoma
- MeSH:
Abdomen;
Adrenal Cortex Neoplasms;
Adrenal Insufficiency;
Adrenocortical Carcinoma;
Adrenocorticotropic Hormone;
Aldosterone;
Biopsy;
Brain;
Humans;
Hydrocortisone;
Male;
Middle Aged;
Neoplasm Metastasis;
Paresis;
Plasma;
Weight Loss
- From:Endocrinology and Metabolism
2011;26(3):243-247
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Adrenocortical carcinoma is often functional and presents with signs and symptoms of adrenal steroid hormone excess. Adrenal insufficiency secondary to bilateral adrenocortical carcinoma is a particularly rare complication. We recently encountered a case of bilateral adrenocortical carcinoma complicated by adrenal insufficiency. A 52-year-old male was transferred to this hospital complaining of general weakness and weight loss. A bilateral adrenal mass was detected on abdomen CT. Plasma cortisol and aldosterone failed to rise during the rapid ACTH stimulation test. The CT-guided adrenal biopsy revealed findings consistent with adrenocortical carcinoma. Left hemiparesis was developed and brain metastasis was detected via brain MRI. Despite the application of gamma knife surgery and chemotherapy, the disease progressed and the patient died.
