Bilateral adrenal pheochromocytoma with a germline L790F mutation in the RET oncogene / 대한외과학회지
Journal of the Korean Surgical Society
;
: 185-189, 2012.
Article
Dans Anglais
| WPRIM
| ID: wpr-50634
ABSTRACT
About ten percent of pheochromocytomas are associated with familial syndrome. Hereditary pheochromocytoma has characteristics of early onset, multifocality and bilaterality. We experienced a case of 44-year-old man with bilateral pheochromocytoma without evidence of medullary thyroid cancer. Genetic test detected a L790F germline mutation of RET oncogene. The author found a necessity for genetic tests in cases of young-age, bilateral pheochromocytoma.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Oncogènes
/
Phéochromocytome
/
Tumeurs de la thyroïde
/
Mutation germinale
Limites du sujet:
Adulte
/
Humains
langue:
Anglais
Texte intégral:
Journal of the Korean Surgical Society
Année:
2012
Type:
Article
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