| Título : |
Clinicopathologic features of familial pituitary adenomas |
| Tipo de documento : |
documento electrónico |
| Autores : |
Luis Vicente Syro Moreno, |
| Fecha de publicación : |
2016 |
| Títulos uniformes : |
Diagnostic Histopathology
|
| Idioma : |
Inglés (eng) |
| Palabras clave : |
AIP Carney complex classification diagnosis DICER1 familial isolated familial syndromes genetics McCune–Albright syndrome multiple endocrine neoplasia type 1 pathology pituitary adenoma pituitary blastoma X-linked acrogigantism syndrome |
| Resumen : |
Pituitary adenomas are common neoplasms. Initially considered as sporadic tumours, some of them are associated with familial syndromes such as familial isolated pituitary adenoma, multiple endocrine neoplasia type 1 and type 4, X-linked acrogigantism syndrome, Carney complex, pheochromocytoma/paraganglioma–pituitary adenoma, pituitary blastoma and McCune–Albright syndrome. They represent a group of diseases with different genetic background and variable phenotype. Here, we summarize the clinicopathological features of pituitary adenomas associated with these familial syndromes. |
| Mención de responsabilidad : |
Luis V. Syro, Fabio Rotondo, Kalman Kovacs, Márta Korbonits |
| Referencia : |
Diag Histop. 2016;22(3):85-91. |
| DOI (Digital Object Identifier) : |
10.1016/j.mpdhp.2016.02.004 |
| En línea : |
http://www.diagnostichistopathology.co.uk/article/S1756-2317(16)00022-0/fulltext |
| Enlace permanente : |
https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_dis |
Clinicopathologic features of familial pituitary adenomas [documento electrónico] / Luis Vicente Syro Moreno, . - 2016. Obra : Diagnostic HistopathologyIdioma : Inglés ( eng)
| Palabras clave : |
AIP Carney complex classification diagnosis DICER1 familial isolated familial syndromes genetics McCune–Albright syndrome multiple endocrine neoplasia type 1 pathology pituitary adenoma pituitary blastoma X-linked acrogigantism syndrome |
| Resumen : |
Pituitary adenomas are common neoplasms. Initially considered as sporadic tumours, some of them are associated with familial syndromes such as familial isolated pituitary adenoma, multiple endocrine neoplasia type 1 and type 4, X-linked acrogigantism syndrome, Carney complex, pheochromocytoma/paraganglioma–pituitary adenoma, pituitary blastoma and McCune–Albright syndrome. They represent a group of diseases with different genetic background and variable phenotype. Here, we summarize the clinicopathological features of pituitary adenomas associated with these familial syndromes. |
| Mención de responsabilidad : |
Luis V. Syro, Fabio Rotondo, Kalman Kovacs, Márta Korbonits |
| Referencia : |
Diag Histop. 2016;22(3):85-91. |
| DOI (Digital Object Identifier) : |
10.1016/j.mpdhp.2016.02.004 |
| En línea : |
http://www.diagnostichistopathology.co.uk/article/S1756-2317(16)00022-0/fulltext |
| Enlace permanente : |
https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_dis |
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Clinicopathologic features of familial pituitary adenomas
