Cargando…
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...
| Autores principales: | , , , , , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Japan
2014
|
| Materias: | |
| 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 |