Feminizing Adrenocortical Carcinoma with Distinct Histopathological Findings.
Feminizing Adrenocortical Carcinoma with Distinct Histopathological Findings.
Intern Med. 2016;55(22):3301-3307
Authors: Hatano M, Takenaka Y, Inoue I, Homma K, Hasegawa T, Sasano H, Awata T, Katayama S
Abstract
We herein present a 60-year-old man with adrenocortical carcinoma who had gynecomastia. An endocrinological examination revealed increased levels of serum estradiol and dehydroepiandrosterone-sulfate (DHEA-S) and reduced levels of free testosterone. Magnetic resonance imaging showed an adrenal tumor with heterogeneous intensity. Iodine-131 adosterol scintigraphy showed an increased uptake at the same site. Because feminizing adrenocortical carcinoma was suspected, right adrenalectomy was performed; the pathological diagnosis was adrenocortical carcinoma. The results of immunostaining indicated a virilizing tumor. Aromatase activity was identified on RT-PCR. As disorganized steroidogenesis is pathologically present in adrenocortical carcinoma, this diagnosis should be made with caution.
PMID: 27853073 [PubMed - in process]
Source: Internal Medicine - Category: Internal Medicine Tags: Intern Med Source Type: research
More News: Adrenocortical Carcinoma | Cancer & Oncology | Carcinoma | Endocrinology | Estradiol | Gynecomastia | Internal Medicine | MRI Scan