| Literature DB >> 22800844 |
Jia-Yan Sheng1, Hong-Chao He, Yu Zhu, Yu-Xuan Wu, Zhou-Jun Shen, Ju-Ping Zhao, Gui Ma, Yun-Ze Xu.
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.Entities:
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Year: 2012 PMID： 22800844
Source DB: PubMed Journal: Chin Med J (Engl) ISSN： 0366-6999 Impact factor: 2.628