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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_display&id=3958 Clinicopathologic features of familial pituitary adenomas [documento electrónico] / Luis Vicente Syro Moreno, . - 2016.
Obra : 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_display&id=3958 Reserva
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