Insulinoma: a case report of a successful resective surgery

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Insulinoma is a pancreatic neuroendocrine tumor that produces hyperinsulinism and causes a severe lowering of blood glucose levels with chronic symptoms such as fainting. It is more common in males and can occur at any age, either as solitary or multiple neoplasms, the latter known to be part of the...

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Detalles Bibliográficos
Autor: Machicado Rivero, Luis Enrique
Formato: artículo
Fecha de Publicación:2023
Institución:Universidad de San Martín de Porres
Repositorio:Horizonte médico
Lenguaje:español
inglés
OAI Identifier:oai:horizontemedico.usmp.edu.pe:article/2391
Enlace del recurso:https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/2391
Nivel de acceso:acceso abierto
Materia:brain stem infarctions
HIV
toxoplasmosis
síndrome de Weber
VIH
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dc.title.none.fl_str_mv Insulinoma: a case report of a successful resective surgery
Insulinoma: reporte de un caso con resección quirúrgica exitosa
title Insulinoma: a case report of a successful resective surgery
spellingShingle Insulinoma: a case report of a successful resective surgery
Machicado Rivero, Luis Enrique
brain stem infarctions
HIV
toxoplasmosis
síndrome de Weber
VIH
toxoplasmosis
title_short Insulinoma: a case report of a successful resective surgery
title_full Insulinoma: a case report of a successful resective surgery
title_fullStr Insulinoma: a case report of a successful resective surgery
title_full_unstemmed Insulinoma: a case report of a successful resective surgery
title_sort Insulinoma: a case report of a successful resective surgery
dc.creator.none.fl_str_mv Machicado Rivero, Luis Enrique
author Machicado Rivero, Luis Enrique
author_facet Machicado Rivero, Luis Enrique
author_role author
dc.subject.none.fl_str_mv brain stem infarctions
HIV
toxoplasmosis
síndrome de Weber
VIH
toxoplasmosis
topic brain stem infarctions
HIV
toxoplasmosis
síndrome de Weber
VIH
toxoplasmosis
description Insulinoma is a pancreatic neuroendocrine tumor that produces hyperinsulinism and causes a severe lowering of blood glucose levels with chronic symptoms such as fainting. It is more common in males and can occur at any age, either as solitary or multiple neoplasms, the latter known to be part of the multiple endocrine neoplasia, type 1 (MEN 1) group. Insulinomas are rare and require resective surgery, with symptoms resolution being the marker of recovery. This article describes a case of insulinoma in a 51-year-old woman with a clinically typical presentation and signs and symptoms of hyperinsulinism. Laboratory tests revealed increased insulin secretion, while magnetic resonance imaging showed features of insulinoma, where the pancreatic tumor could be seen. This case was treated by surgical resection of the pancreatic tumor during an exploratory laparotomy, using the enucleation technique, which is described in detail herein. There were no intraoperative or postoperative complications, i.e., the result was successful in terms of health recovery. This surgical technique is used at Hospital Nacional Arzobispo Loayza in Lima, Peru, when facing cases such as the one described. This type of neoplasm is very uncommon, so it should be considered highly suspicious and, in this case, the images were essential for choosing the surgical resection. Other cases of insulinoma have been treated surgically at the Hospital; moreover at least one case of nesidioblastosis could not receive an adequate treatment.
publishDate 2023
dc.date.none.fl_str_mv 2023-12-18
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/2391
10.24265/horizmed.2023.v23n4.10
url https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/2391
identifier_str_mv 10.24265/horizmed.2023.v23n4.10
dc.language.none.fl_str_mv spa
eng
language spa
eng
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dc.rights.none.fl_str_mv Derechos de autor 2023 Horizonte Médico (Lima)
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rights_invalid_str_mv Derechos de autor 2023 Horizonte Médico (Lima)
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dc.publisher.none.fl_str_mv Universidad de San Martín de Porres. Facultad de Medicina Humana
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dc.source.none.fl_str_mv Horizonte Médico (Lima); Vol. 23 No. 4 (2023): Octubre-Diciembre; e2391
Horizonte Médico (Lima); Vol. 23 Núm. 4 (2023): Octubre-Diciembre; e2391
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spelling Insulinoma: a case report of a successful resective surgeryInsulinoma: reporte de un caso con resección quirúrgica exitosaMachicado Rivero, Luis Enriquebrain stem infarctionsHIVtoxoplasmosis síndrome de WeberVIHtoxoplasmosis Insulinoma is a pancreatic neuroendocrine tumor that produces hyperinsulinism and causes a severe lowering of blood glucose levels with chronic symptoms such as fainting. It is more common in males and can occur at any age, either as solitary or multiple neoplasms, the latter known to be part of the multiple endocrine neoplasia, type 1 (MEN 1) group. Insulinomas are rare and require resective surgery, with symptoms resolution being the marker of recovery. This article describes a case of insulinoma in a 51-year-old woman with a clinically typical presentation and signs and symptoms of hyperinsulinism. Laboratory tests revealed increased insulin secretion, while magnetic resonance imaging showed features of insulinoma, where the pancreatic tumor could be seen. This case was treated by surgical resection of the pancreatic tumor during an exploratory laparotomy, using the enucleation technique, which is described in detail herein. There were no intraoperative or postoperative complications, i.e., the result was successful in terms of health recovery. This surgical technique is used at Hospital Nacional Arzobispo Loayza in Lima, Peru, when facing cases such as the one described. This type of neoplasm is very uncommon, so it should be considered highly suspicious and, in this case, the images were essential for choosing the surgical resection. Other cases of insulinoma have been treated surgically at the Hospital; moreover at least one case of nesidioblastosis could not receive an adequate treatment.El insulinoma es un tumor endocrino del páncreas, el cual produce hiperinsulinismo y provoca disminución severa de la glucemia, con síntomas crónicos como desvanecimiento. Es más frecuente en varones y puede presentarse a cualquier edad, ya sea como neoplasias solitarias o múltiples, estas últimas conocidas por formar parte del grupo de neoplasias endocrinas múltiples tipo 1 (MEN 1). Los insulinomas son de rara presentación y requieren tratamiento quirúrgico resectivo; la resolución de los síntomas es el marcador de curación. En la presente publicación, se describe un caso de insulinoma en una mujer de 51 años, de presentación típica desde el punto de vista clínico, con síntomas y signos de hiperinsulinismo. Los exámenes de laboratorio indican un aumento de la secreción de insulina, mientras que las imágenes por resonancia magnética muestran características del insulinoma, donde se puede apreciar la tumoración pancreática. Este caso se trató mediante resección quirúrgica por medio de laparotomía exploratoria, utilizando la técnica de enucleación del tumor pancreático, la cual se describe al detalle en la publicación; no se presentaron complicaciones intraoperatorias ni posoperatorias, es decir, desde el punto de vista curativo, el resultado fue exitoso. Esta es la técnica quirúrgica que se emplea en el Hospital Nacional Arzobispo Loayza en Lima, Perú, ante casos como el descrito. Este tipo de neoplasia es muy poco común, por lo que se le debe considerar de alta sospecha y, en este caso, las imágenes fueron fundamentales para optar por la resección quirúrgica. En el hospital Arzobispo Loayza se han tratado otros casos de insulinoma mediante cirugía; asimismo, se ha presentado, al menos, un caso de nesidioblastosis, en donde no se pudo administrar un tratamiento adecuado al paciente. Universidad de San Martín de Porres. Facultad de Medicina Humana2023-12-18info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdftext/xmltext/htmlapplication/pdftext/xmlhttps://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/239110.24265/horizmed.2023.v23n4.10Horizonte Médico (Lima); Vol. 23 No. 4 (2023): Octubre-Diciembre; e2391Horizonte Médico (Lima); Vol. 23 Núm. 4 (2023): Octubre-Diciembre; e2391Horizonte Médico (Lima); v. 23 n. 4 (2023): Octubre-Diciembre; e23912227-35301727-558Xreponame:Horizonte médicoinstname:Universidad de San Martín de Porresinstacron:USMPspaenghttps://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/2391/1729https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/2391/1628https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/2391/1672https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/2391/1734https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/2391/1758Derechos de autor 2023 Horizonte Médico (Lima)https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:horizontemedico.usmp.edu.pe:article/23912023-12-18T14:03:13Z
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