Primary Meningeal Pheochromocytoma: A Case Report
Journal of the Korean Radiological Society
;
: 311-313, 2007.
Artigo
em Coreano
| WPRIM
| ID: wpr-160000
ABSTRACT
Pheochromocytoma is a rare endocrine tumor arising from the chromaffin tissue, and it is able to produce and secrete catecholamines. Lymph nodes, liver, lung and bone are the most frequent sites of metastasis. We report here on a case of pheochromocytoma arising from the dura in a patient who was surgically treated for bilateral pheochromocytoma five years previously.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Feocromocitoma
/
Catecolaminas
/
Fígado
/
Pulmão
/
Linfonodos
/
Metástase Neoplásica
Limite:
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Radiological Society
Ano de publicação:
2007
Tipo de documento:
Artigo
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