A novel RET mutation identified in a patient with pheochromocytoma and renal cell carcinoma / 고신대학교의과대학학술지
Kosin Medical Journal
;
: 446-453, 2018.
Artigo
em Inglês
| WPRIM
| ID: wpr-739004
ABSTRACT
Pheochromocytomas might be sporadic or genetic. Genetic pheochromocytoma is associated with multiple endocrine neoplasia (MEN) type 2A, MEN type 2B, and von Hippel-Lindau (VHL) disease. RET mutations are identified in more than 90% of index cases of MEN2 and familial medullary thyroid cancer and in about 4–12% of apparent sporadic cases. Here, we report a 54-year-old man presenting with pheochromocytoma and renal cell carcinoma, who was identified as having a novel missense RET mutation.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Feocromocitoma
/
Neoplasia Endócrina Múltipla
/
Neoplasias da Glândula Tireoide
/
Carcinoma de Células Renais
Limite:
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Kosin Medical Journal
Ano de publicação:
2018
Tipo de documento:
Artigo
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