1.
Chinese Medical Journal
;
(24): 1672-1674, 2012.
Article
in English
| WPRIM
| ID: wpr-324913
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.