Myxoid adrenal cortical tumor: report of four cases

被引：3
|
作者：
Sheng Jia-yan [1 ]
He Hong-chao [1 ]
Zhu Yu [1 ]
Wu Yu-xuan [1 ]
Shen Zhou-jun [1 ]
Zhao Ju-ping [1 ]
Ma Gui [1 ]
Xu Yun-ze [1 ]
机构：
[1] Shanghai Jiao Tong Univ, Ruijin Hosp, Sch Med, Dept Urol, Shanghai 200025, Peoples R China
来源：
CHINESE MEDICAL JOURNAL | 2012年 / 125卷 / 09期
关键词：
myxoid adrenal cortical tumor; endocrine metabolic; clinicopathological and immunohistochemical feature; prognosis; ADRENOCORTICAL CARCINOMA;
D O I：
10.3760/cma.j.issn.0366-6999.2012.09.030
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
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. Chin Med J 2012;125(9):1672-1674
引用
收藏
页码：1672 / 1674
页数：3
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