Myxoid adrenal cortical tumor: report of four cases / 中华医学杂志(英文版)
Chin. med. j
; Chin. med. j;(24): 1672-1674, 2012.
Article
en En
| WPRIM
| ID: wpr-324913
Biblioteca responsable:
WPRO
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.
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Cirugía General
/
Biomarcadores de Tumor
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Neoplasias de la Corteza Suprarrenal
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Diagnóstico
/
Metabolismo
Tipo de estudio:
Diagnostic_studies
Límite:
Adult
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Aged
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Female
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Humans
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Male
Idioma:
En
Revista:
Chin. med. j
Año:
2012
Tipo del documento:
Article