Incidentalomas suprarrenales: experiencia clínica en los hospitales de Castilla-La Mancha

ObjectiveThe management of incidentally discovered adrenal masses (incidentalomas) remains controversial. Our objective was to describe the demographic and clinical characteristics of a series of patients with adrenal incidentalomas attended in several hospitals of Castilla-La Mancha, and their diag...

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Autores: Lamas Oliveira, Cristina, Palma, Mercedes, Martín, David, Álvarez de Frutos, Visitación, López, María, Marco, Amparo
Tipo de recurso: artículo
Fecha de publicación:2009
País:España
Institución:Universidad de Castilla-La Mancha
Repositorio:RUIdeRA. Repositorio Institucional de la UCLM
OAI Identifier:oai:ruidera.uclm.es:10578/33329
Acceso en línea:https://hdl.handle.net/10578/33329
Access Level:acceso abierto
Palabra clave:Adrenal incidentalomas
Feocromocitoma
Hiperaldosteronismo primario
Incidentalomas suprarrenales
Pheochromocytoma
Primary aldosteronism
Síndrome de Cushing subclínico
Subclinical Cushing syndrome
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spelling Incidentalomas suprarrenales: experiencia clínica en los hospitales de Castilla-La ManchaLamas Oliveira, CristinaPalma, MercedesMartín, DavidÁlvarez de Frutos, VisitaciónLópez, MaríaMarco, AmparoAdrenal incidentalomasFeocromocitomaHiperaldosteronismo primarioIncidentalomas suprarrenalesPheochromocytomaPrimary aldosteronismSíndrome de Cushing subclínicoSubclinical Cushing syndromeObjectiveThe management of incidentally discovered adrenal masses (incidentalomas) remains controversial. Our objective was to describe the demographic and clinical characteristics of a series of patients with adrenal incidentalomas attended in several hospitals of Castilla-La Mancha, and their diagnostic and therapeutic management.Material and methodsData were obtained by reviewing the patients’ medical charts.ResultsA total of 270 patients were included (28.1% from Toledo, 25.9% from Albacete, 24.1% from Ciudad Real, 15.9% from Cuenca and 5.9% from Guadalajara). The mean age was 60.3 ± 12 and 53.3% were women. Overweight or obesity were found in 80.6%, hypertension in 55.8%, diabetes mellitus in 25.6%, impaired fasting glucose or impaired glucose tolerance in 15.6%, osteopenia in 31.5% and osteoporosis in 20.4%. These percentages were similar in patients with subclinical Cushing's syndrome. Diameter was less than 3 cm in 66% of the tumors, and more than 4 cm in 14.3%. Eighty-five percent of the tumors were detected by computed tomography. After a median follow-up of 28.8 months, 6% of nonfunctioning adenomas progressed to subclinical Cushing's syndrome, tumoral enlargement of more than 1 cm was found in 9.4% and a contralateral mass developed in 8.9%. Surgical adrenalectomy was performed in 14.4% of the patients.ConclusionsOur study confirms the favorable outcome in most patients with adrenal incidentalomas and contributes to a better understanding of this clinical entity.ObjetivoEl manejo de las masas suprarrenales descubiertas de manera incidental (incidentalomas) sigue siendo controvertido. El objetivo de este trabajo es describir las características demográficas y clínicas, así como el manejo diagnóstico-terapéutico, de una serie de pacientes con incidentalomas suprarrenales atendidos en los principales hospitales de Castilla-La Mancha.Material y métodosLos datos se recogieron mediante revisión de historias clínicas.ResultadosSe revisaron las historias clínicas de 270 pacientes (el 28,1% de Toledo, el 25,9% de Albacete, el 24,1% de Ciudad Real, el 15,9% de Cuenca y el 5,9% de Guadalajara), con media de edad de 60,3 ± 12 años y de los que el 53,3% eran mujeres. El 80,6% presentaba sobrepeso u obesidad; el 55,8%, hipertensión arterial; el 25,6%, diabetes mellitus; el 15,6%, alteración de la glucemia en ayunas o intolerancia hidrocarbonada; el 31,5%, osteopenia, y el 20,4%, osteoporosis; estos porcentajes son similares en los pacientes con síndrome de Cushing subclínico. El 66% de los tumores medían menos de 3 cm y el 14,3% más de 4 cm. El 85% fueron detectados por tomografía computarizada. Tras una mediana de seguimiento de 28,8 meses el 6% de los adenomas no funcionantes evolucionaron a un síndrome de Cushing subclínico, en un 9,4% de los casos el diámetro de la masa aumentó más de 1 cm y en un 8,9% apareció una masa contralateral. El 14,4% de los pacientes se sometieron a suprarrenalectomía quirúrgica.ConclusionesNuestro estudio confirma la evolución favorable de la mayoría de los pacientes con incidentalomas suprarrenales y contribuye a un mejor conocimiento de esta entidad clínica.Elsevier202420242009info:eu-repo/semantics/articleapplication/pdfapplication/pdfhttps://hdl.handle.net/10578/33329reponame:RUIdeRA. Repositorio Institucional de la UCLMinstname:Universidad de Castilla-La ManchaEspañolinfo:eu-repo/semantics/openAccessoai:ruidera.uclm.es:10578/333292026-05-27T07:36:41Z
dc.title.none.fl_str_mv Incidentalomas suprarrenales: experiencia clínica en los hospitales de Castilla-La Mancha
title Incidentalomas suprarrenales: experiencia clínica en los hospitales de Castilla-La Mancha
spellingShingle Incidentalomas suprarrenales: experiencia clínica en los hospitales de Castilla-La Mancha
Lamas Oliveira, Cristina
Adrenal incidentalomas
Feocromocitoma
Hiperaldosteronismo primario
Incidentalomas suprarrenales
Pheochromocytoma
Primary aldosteronism
Síndrome de Cushing subclínico
Subclinical Cushing syndrome
title_short Incidentalomas suprarrenales: experiencia clínica en los hospitales de Castilla-La Mancha
title_full Incidentalomas suprarrenales: experiencia clínica en los hospitales de Castilla-La Mancha
title_fullStr Incidentalomas suprarrenales: experiencia clínica en los hospitales de Castilla-La Mancha
title_full_unstemmed Incidentalomas suprarrenales: experiencia clínica en los hospitales de Castilla-La Mancha
title_sort Incidentalomas suprarrenales: experiencia clínica en los hospitales de Castilla-La Mancha
dc.creator.none.fl_str_mv Lamas Oliveira, Cristina
Palma, Mercedes
Martín, David
Álvarez de Frutos, Visitación
López, María
Marco, Amparo
author Lamas Oliveira, Cristina
author_facet Lamas Oliveira, Cristina
Palma, Mercedes
Martín, David
Álvarez de Frutos, Visitación
López, María
Marco, Amparo
author_role author
author2 Palma, Mercedes
Martín, David
Álvarez de Frutos, Visitación
López, María
Marco, Amparo
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Adrenal incidentalomas
Feocromocitoma
Hiperaldosteronismo primario
Incidentalomas suprarrenales
Pheochromocytoma
Primary aldosteronism
Síndrome de Cushing subclínico
Subclinical Cushing syndrome
topic Adrenal incidentalomas
Feocromocitoma
Hiperaldosteronismo primario
Incidentalomas suprarrenales
Pheochromocytoma
Primary aldosteronism
Síndrome de Cushing subclínico
Subclinical Cushing syndrome
description ObjectiveThe management of incidentally discovered adrenal masses (incidentalomas) remains controversial. Our objective was to describe the demographic and clinical characteristics of a series of patients with adrenal incidentalomas attended in several hospitals of Castilla-La Mancha, and their diagnostic and therapeutic management.Material and methodsData were obtained by reviewing the patients’ medical charts.ResultsA total of 270 patients were included (28.1% from Toledo, 25.9% from Albacete, 24.1% from Ciudad Real, 15.9% from Cuenca and 5.9% from Guadalajara). The mean age was 60.3 ± 12 and 53.3% were women. Overweight or obesity were found in 80.6%, hypertension in 55.8%, diabetes mellitus in 25.6%, impaired fasting glucose or impaired glucose tolerance in 15.6%, osteopenia in 31.5% and osteoporosis in 20.4%. These percentages were similar in patients with subclinical Cushing's syndrome. Diameter was less than 3 cm in 66% of the tumors, and more than 4 cm in 14.3%. Eighty-five percent of the tumors were detected by computed tomography. After a median follow-up of 28.8 months, 6% of nonfunctioning adenomas progressed to subclinical Cushing's syndrome, tumoral enlargement of more than 1 cm was found in 9.4% and a contralateral mass developed in 8.9%. Surgical adrenalectomy was performed in 14.4% of the patients.ConclusionsOur study confirms the favorable outcome in most patients with adrenal incidentalomas and contributes to a better understanding of this clinical entity.
publishDate 2009
dc.date.none.fl_str_mv 2009
2024
2024
dc.type.none.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://hdl.handle.net/10578/33329
url https://hdl.handle.net/10578/33329
dc.language.none.fl_str_mv Español
language_invalid_str_mv Español
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:RUIdeRA. Repositorio Institucional de la UCLM
instname:Universidad de Castilla-La Mancha
instname_str Universidad de Castilla-La Mancha
reponame_str RUIdeRA. Repositorio Institucional de la UCLM
collection RUIdeRA. Repositorio Institucional de la UCLM
repository.name.fl_str_mv
repository.mail.fl_str_mv
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