Searchable abstracts of presentations at key conferences in endocrinology

ea0029p26 | Adrenal cortex | ICEECE2012

Follow-up of nonsurgical nonfunctioning adrenal adenomas at five years

Ramos-Prol A. , Camara-Gomez R. , Leon-de Zayas B. , Garcia-Malpartida K. , Campos-Alborg V. , del Olmo-Garcia M. , Merino-Torres J.

The management of nonfunctioning adrenal masses is controversial. The size is usually the only criterion for surgical treatment. The objective was to study the progression of the tumor size and the follow-up of several cardiovascular risk parameters in patients with nonsurgical nonfunctioning adrenal masses.Retrospective longitudinal observational study of 24 patients (54.2% men) with nonfunctioning adenomas followed for five years without surgical treat...

ea0029p27 | Adrenal cortex | ICEECE2012

Importance of the genetic study in fertile women with nonclassical congenital adrenal hyperplasia

Rubio-Almanza M. , Navas-de Solis S. , Tenes-Rodrigo S. , Querol Ripoll R. , Perez-Lazaro A. , del Olmo-Garcia M. , Merino-Torres J.

The Nonclassical Congenital Adrenal Hyperplasia (NCCAH) is an autosomal recessive disorder. The importance of the diagnosis in fertile women relies in its therapeutic implications, genetic counseling and antenatal care during pregnancy. Diagnosis is established by the presence of basal 17-OH-progesterone (17-OHP) levels ≧6 ng/ml or stimulated after ACTH test ≧15 ng/ml. Basal values between 2-6 ng/ml or stimulated between 10–15 ng/ml would require further con...

ea0029p880 | Endocrine tumours and neoplasia | ICEECE2012

Neuroendocrine tumors of the gastrointestinal tract: a descriptive study

Leon de Zayas B. , del Olmo Garcia M. , Ramos Prol A. , Argente Pla M. , Munoz Vicente M. , Gilsanz Peral A. , Merino Torres J.

Introduction and objective: Neuroendocrine tumors (NETs) are relatively rare tumors. The majority are located in the gastrointestinal (GI) tract and bronchopulmonary system. The aim of this report is to study the characteristics of gastrointestinal NETs at diagnosis.Material and methods: Descriptive study about 18 patients diagnosed of gastrointestinal NETs during 1993–2011 in our hospital. Data regarding demographic, clinical, analytical, anatomopa...

ea0026p57 | Endocrine tumours and neoplasia | ECE2011

Clinicopathological characteristics of pancreatic neuroendocrine tumors at diagnosis

Argente Pla M , Del Olmo Garcia M I , Almanza M Rubio , Herraiz A Moya , Huerta A Segura , Prol A Ramos , Gomez R Camara , Merino Torres J F

Introduction and objective: Neuroendocrine tumors (NETs) are a rare kind of tumor that can have various locations. Pancreatic location is the most common after the gastrointestinal tract. The aim of this report is to study the characteristics of neuroendocrine tumors located in the pancreatic gland (pNETs) at diagnosis.Material and methods: Descriptive and retrospective study about 22 patients diagnosed of pNET during the period 1993–2010 in our hos...

ea0026p211 | Pituitary | ECE2011

Gender-related differences in prolactinomas

Ramos-Prol A , Camara-Gomez R , Leon-de Zayas B , Beltran A , Simal J A , Argente-Pla M , del Olmo-Garcia M I , Merino-Torres J F

Introduction: It has been previously described that prolactinomas may have a more aggressive behaviour in men than in women.Methods: We performed a retrospective study in 59 patients diagnosed of prolactinoma (19 men). The variables collected were: age at diagnosis, clinical presentation, tumor size and stage (Hardy classification) and treatment response. The results were compared between both genders.Results: Age at diagnosis was ...