3 búsqueda de la palabra clave 'multiple endocrine neoplasia type 1'

Clinicopathologic features of familial pituitary adenomas / Luis Vicente Syro Moreno  

Público ISBD 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

Reservar este documento

Ejemplares(1)

Código de barras	Número de Ubicación	Tipo de medio	Ubicación	Sección	Estado
DD000544	AC-2016-019	Archivo digital	Producción Científica	Artículos científicos	Disponible

Progress in the Diagnosis and Classification of Pituitary Adenomas / Luis Vicente Syro Moreno  

Público ISBD Título : Progress in the Diagnosis and Classification of Pituitary Adenomas Tipo de documento : documento electrónico Autores : Luis Vicente Syro Moreno, Fecha de publicación : 2015 Títulos uniformes : Frontiers in Endocrinology Idioma : Inglés (eng) Palabras clave : Diagnosis  genetics  pathology  acromegaly  multiple endocrine neoplasia type 1  pituitary adenoma  familial isolated  carney complex Resumen : Pituitary adenomas are common neoplasms. Their classification is based upon size, invasion of adjacent structures, sporadic or familial cases, biochemical activity, clinical manifestations, morphological characteristics, response to treatment and recurrence. Although they are considered benign tumors, some of them are difficult to treat due to their tendency to recur despite standardized treatment. Functional tumors present other challenges for normalizing their biochemical activity. Novel approaches for early diagnosis, as well as different perspectives on classification, may help to identify subgroups of patients with similar characteristics, creating opportunities to match each patient with the best personalized treatment option. In this paper, we present the progress in the diagnosis and classification of different subgroups of patients with pituitary tumors that may be managed with specific considerations according to their tumor subtype. Mención de responsabilidad : Luis V Syro, Fabio Rotondo, Alex Ramirez, Antonio Di Ieva, Murat Aydin Sav, Lina M Restrepo, Carlos A Serna, Kalman Kovacs Referencia : Front Endocrinol (Lausanne). 2015 Jun 12;6:97. DOI (Digital Object Identifier) : 10.3389/fendo.2015.00097 PMID : 26124750 En línea : https://www.frontiersin.org/articles/10.3389/fendo.2015.00097/full Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3893 Progress in the Diagnosis and Classification of Pituitary Adenomas [documento electrónico] / Luis Vicente Syro Moreno,  . - 2015. Obra : Frontiers in Endocrinology Idioma : Inglés (eng) Palabras clave : Diagnosis  genetics  pathology  acromegaly  multiple endocrine neoplasia type 1  pituitary adenoma  familial isolated  carney complex Resumen : Pituitary adenomas are common neoplasms. Their classification is based upon size, invasion of adjacent structures, sporadic or familial cases, biochemical activity, clinical manifestations, morphological characteristics, response to treatment and recurrence. Although they are considered benign tumors, some of them are difficult to treat due to their tendency to recur despite standardized treatment. Functional tumors present other challenges for normalizing their biochemical activity. Novel approaches for early diagnosis, as well as different perspectives on classification, may help to identify subgroups of patients with similar characteristics, creating opportunities to match each patient with the best personalized treatment option. In this paper, we present the progress in the diagnosis and classification of different subgroups of patients with pituitary tumors that may be managed with specific considerations according to their tumor subtype. Mención de responsabilidad : Luis V Syro, Fabio Rotondo, Alex Ramirez, Antonio Di Ieva, Murat Aydin Sav, Lina M Restrepo, Carlos A Serna, Kalman Kovacs Referencia : Front Endocrinol (Lausanne). 2015 Jun 12;6:97. DOI (Digital Object Identifier) : 10.3389/fendo.2015.00097 PMID : 26124750 En línea : https://www.frontiersin.org/articles/10.3389/fendo.2015.00097/full Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3893

Reserva

Reservar este documento

Ejemplares(1)

Código de barras	Número de Ubicación	Tipo de medio	Ubicación	Sección	Estado
DD000473	AC-2015-026	Archivo digital	Producción Científica	Artículos científicos	Disponible

Pituitary tumors in patients with MEN1 syndrome / Luis Vicente Syro Moreno  

Público ISBD Título : Pituitary tumors in patients with MEN1 syndrome Tipo de documento : documento electrónico Autores : Luis Vicente Syro Moreno, Fecha de publicación : 2012 Títulos uniformes : Clinics (Sao Paulo) Idioma : Inglés (eng) Palabras clave : Pituitary neoplasms  multiple endocrine neoplasia type 1  review  genetics Resumen : We briefly review the characteristics of pituitary tumors associated with multiple endocrine neoplasia type 1. Multiple endocrine neoplasia type 1 is an autosomal-dominant disorder most commonly characterized by tumors of the pituitary, parathyroid, endocrine-gastrointestinal tract, and pancreas. A MEDLINE search for all available publications regarding multiple endocrine neoplasia type 1 and pituitary adenomas was undertaken. The prevalence of pituitary tumors in multiple endocrine neoplasia type 1 may vary from 10% to 60% depending on the studied series, and such tumors may occur as the first clinical manifestation of multiple endocrine neoplasia type 1 in 25% of sporadic and 10% of familial cases. Patients were younger and the time between initial and subsequent multiple endocrine neoplasia type 1 endocrine lesions was significantly longer when pituitary disease was the initial manifestation of multiple endocrine neoplasia type 1. Tumors were larger and more invasive and clinical manifestations related to the size of the pituitary adenoma were significantly more frequent in patients with multiple endocrine neoplasia type 1 than in subjects with non-multiple endocrine neoplasia type 1. Normalization of pituitary hypersecretion was much less frequent in patients with multiple endocrine neoplasia type 1 than in subjects with non-multiple endocrine neoplasia type 1. Pituitary tumors in patients with multiple endocrine neoplasia type 1 syndrome tend to be larger, invasive and more symptomatic, and they tend to occur in younger patients when they are the initial presentation of multiple endocrine neoplasia type 1. Mención de responsabilidad : Luis V Syro, Bernd W Scheithauer, Kalman Kovacs, Rodrigo A Toledo, Francisco J Londoño, Leon D Ortiz, Fabio Rotondo, Eva Horvath, Humberto Uribe Referencia : Clinics (Sao Paulo). 2012;67 Suppl 1:43-8. DOI (Digital Object Identifier) : 10.6061/clinics/2012(Sup01)09 PMID : 22584705 En línea : https://www.revistas.usp.br/clinics/article/view/19720 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3610 Pituitary tumors in patients with MEN1 syndrome [documento electrónico] / Luis Vicente Syro Moreno,  . - 2012. Obra : Clinics (Sao Paulo) Idioma : Inglés (eng) Palabras clave : Pituitary neoplasms  multiple endocrine neoplasia type 1  review  genetics Resumen : We briefly review the characteristics of pituitary tumors associated with multiple endocrine neoplasia type 1. Multiple endocrine neoplasia type 1 is an autosomal-dominant disorder most commonly characterized by tumors of the pituitary, parathyroid, endocrine-gastrointestinal tract, and pancreas. A MEDLINE search for all available publications regarding multiple endocrine neoplasia type 1 and pituitary adenomas was undertaken. The prevalence of pituitary tumors in multiple endocrine neoplasia type 1 may vary from 10% to 60% depending on the studied series, and such tumors may occur as the first clinical manifestation of multiple endocrine neoplasia type 1 in 25% of sporadic and 10% of familial cases. Patients were younger and the time between initial and subsequent multiple endocrine neoplasia type 1 endocrine lesions was significantly longer when pituitary disease was the initial manifestation of multiple endocrine neoplasia type 1. Tumors were larger and more invasive and clinical manifestations related to the size of the pituitary adenoma were significantly more frequent in patients with multiple endocrine neoplasia type 1 than in subjects with non-multiple endocrine neoplasia type 1. Normalization of pituitary hypersecretion was much less frequent in patients with multiple endocrine neoplasia type 1 than in subjects with non-multiple endocrine neoplasia type 1. Pituitary tumors in patients with multiple endocrine neoplasia type 1 syndrome tend to be larger, invasive and more symptomatic, and they tend to occur in younger patients when they are the initial presentation of multiple endocrine neoplasia type 1. Mención de responsabilidad : Luis V Syro, Bernd W Scheithauer, Kalman Kovacs, Rodrigo A Toledo, Francisco J Londoño, Leon D Ortiz, Fabio Rotondo, Eva Horvath, Humberto Uribe Referencia : Clinics (Sao Paulo). 2012;67 Suppl 1:43-8. DOI (Digital Object Identifier) : 10.6061/clinics/2012(Sup01)09 PMID : 22584705 En línea : https://www.revistas.usp.br/clinics/article/view/19720 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3610

Reserva

Reservar este documento

Ejemplares(1)

Código de barras	Número de Ubicación	Tipo de medio	Ubicación	Sección	Estado
DD000180	AC-2012-020	Archivo digital	Producción Científica	Artículos científicos	Disponible