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Myxoid adrenal cortical tumor: report of four cases
Jia-Yan Sheng1, Hong-Chao He, Yu Zhu
1Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Chinese Medical Journal
|July 18, 2012
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.
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