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

页码：1672 / 1674

页数：3

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