Pheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a case

We report a rare case with pheochromocytoma as the first manifestation of multiple endocrine neoplasia type 2A with RET mutation S891A. Bilateral pheochromocytomas were identified in a 54-year-old woman. Screening for RET revealed a rare S891A mutation located in the intracellular tyrosine kinase do...

Descripción completa

Detalles Bibliográficos
Autores principales: Hibi, Yatsuka, Ohye, Tamae, Ogawa, Kimio, Shimizu, Yoshimi, Shibata, Masahiro, Kagawa, Chikara, Mizuno, Yutaka, Uchino, Shinya, Kosugi, Shinji, Kurahashi, Hiroki, Iwase, Katsumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194010/
https://www.ncbi.nlm.nih.gov/pubmed/24449023
http://dx.doi.org/10.1007/s00595-013-0826-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194010/
https://www.ncbi.nlm.nih.gov/pubmed/24449023
http://dx.doi.org/10.1007/s00595-013-0826-8

Ejemplares similares