Myxoid adrenal cortical tumor: report of four cases.
- Author:
Jia-Yan SHENG
1
;
Hong-Chao HE
;
Yu ZHU
;
Yu-Xuan WU
;
Zhou-Jun SHEN
;
Ju-Ping ZHAO
;
Gui MA
;
Yun-Ze XU
Author Information
1. Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
- Publication Type:Case Reports
- MeSH:
Adrenal Cortex Neoplasms;
diagnosis;
metabolism;
surgery;
Adult;
Aged;
Biomarkers, Tumor;
metabolism;
Female;
Humans;
Male;
Middle Aged
- From:
Chinese Medical Journal
2012;125(9):1672-1674
- CountryChina
- Language:English
-
Abstract:
Myxoid adrenocortical neoplasms are rare. Surgical resection of the mass is the first-line therapy. Here we reported a total of four patients, aged 44–66 years, diagnosed with myxoid adrenocortical tumor. The clinical characteristics and immunohistochemical features of the tumor are discussed in the current literature.
