Myxoid adrenal cortical tumor: report of four cases

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...

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Veröffentlicht in:Chinese medical journal 2012-05, Vol.125 (9), p.1672-1674
Hauptverfasser: Sheng, Jia-Yan, He, Hong-Chao, Zhu, Yu, Wu, Yu-Xuan, Shen, Zhou-Jun, Zhao, Ju-Ping, Ma, Gui, Xu, Yun-Ze
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Sprache:eng
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Zusammenfassung: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.
ISSN:0366-6999
2542-5641
DOI:10.3760/cma.j.issn.0366-6999.2012.09.030