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dc.creatorManterola, Carlos
dc.date2015-09-01
dc.date.accessioned2020-10-07T22:50:29Z
dc.date.available2020-10-07T22:50:29Z
dc.identifierhttps://revistas.uautonoma.cl/index.php/ijmss/article/view/184
dc.identifier10.32457/ijmss.2015.032
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/154285
dc.descriptionPancreatic insulinomas (IP), are uncommon tumors that come from the beta cells of pancreatic islets, which are characterized by producing insulin excessively, therefore causing hypoglycemia; which is manifested by neuroglycopenic and autonomic symptoms. IP diagnosis is proposed by Whipple's triad, characterized by hypoglycemia, neuroglycopenic symptoms and the reversal of the symptoms following the administration of glucose. Surgery remains the treatment of choice for IP, either by laparotomy or laparoscopy, performing enucleation or segmental pancreatectomies. These procedures are not free of complications, most notably are pancreatic fistula, and pseudocyst formation, and the development of diabetes mellitus. The aim of this paper is to report the personal experience in treating consecutive patients with PI and discuss the related literature.en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherUniversidad Autónoma de Chileen-US
dc.relationhttps://revistas.uautonoma.cl/index.php/ijmss/article/view/184/181
dc.rightsCopyright (c) 2020 International Journal of Medical and Surgical Sciencesen-US
dc.sourceInternational Journal of Medical and Surgical Sciences; Vol. 2 No. 3 (2015): September 2015; 571-577en-US
dc.sourceInternational Journal of Medical and Surgical Sciences; Vol. 2 Núm. 3 (2015): September 2015; 571-577es-ES
dc.source0719-532X
dc.source0719-3904
dc.subjectInsulinomaen-US
dc.subjectInsulinoma/diagnosisen-US
dc.subjectInsulinoma/surgeryen-US
dc.subjectPancreatectomyen-US
dc.titlePancreatic Insulinoma. About a Personal Experience of 3 Casesen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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