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Vague neuroglycopenic complaints camouflage diagnosis of adolescent insulinoma: a case report

BACKGROUND: Insulinoma is a rare diagnosis in the general population with estimates of 1 in 250,000 people per year. Reports of these pancreatic islet cell tumors are even more unusual in children and adolescents. Chronic hypoglycemia due to an insulinoma often presents with neuroglycopenic symptoms...

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Autores principales: Halpin, Kelsee, McDonough, Ryan, Alba, Patria, Halpin, Jared, Singh, Vivekanand, Yan, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967349/
https://www.ncbi.nlm.nih.gov/pubmed/27478444
http://dx.doi.org/10.1186/s13633-016-0032-8
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author Halpin, Kelsee
McDonough, Ryan
Alba, Patria
Halpin, Jared
Singh, Vivekanand
Yan, Yun
author_facet Halpin, Kelsee
McDonough, Ryan
Alba, Patria
Halpin, Jared
Singh, Vivekanand
Yan, Yun
author_sort Halpin, Kelsee
collection PubMed
description BACKGROUND: Insulinoma is a rare diagnosis in the general population with estimates of 1 in 250,000 people per year. Reports of these pancreatic islet cell tumors are even more unusual in children and adolescents. Chronic hypoglycemia due to an insulinoma often presents with neuroglycopenic symptoms that can easily be overlooked, especially in adolescents where nonspecific complaints are common. This may result in delayed diagnosis with prolonged periods of untreated hypoglycemia and associated complications. The rarity of pediatric insulinoma, vagueness of presenting symptoms, and challenge of tumor localization make insulinoma a true diagnostic quandary for clinicians. CASE PRESENTATION: In this report, we present a 15-year-old female who visited her primary care provider complaining of intermittent episodes of altered mental status including fatigue, irritability, and poor concentration. Her outpatient management included routine laboratory studies, drug screening, electroencephalogram (EEG), valproic acid initiation, CT scan of the abdomen, and endoscopic ultrasound with documentation of hypoglycemia, but otherwise inconclusive results. The patient was admitted to a tertiary children’s hospital with severe refractory hypoglycemia 8 months after the initial evaluation. A serum critical sample was obtained and magnetic resonance imaging (MRI) of the abdomen performed which confirmed the presence of a pancreatic mass ultimately identified as an insulinoma. She went on to have surgical resection of her tumor resulting in complete resolution of her hypoglycemia and associated symptoms. CONCLUSION: Within this report we demonstrate the importance of being vigilant for fasting hypoglycemia secondary to insulinoma even when the patient presents with nonspecific symptoms such as fatigue, irritability, or problems with concentration. If these neuroglycopenic complaints are unnoticed or misdiagnosed, patients with a potentially curable disease are put at risk of neurologic injury, or even death, due to untreated severe hypoglycemia.
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spelling pubmed-49673492016-07-31 Vague neuroglycopenic complaints camouflage diagnosis of adolescent insulinoma: a case report Halpin, Kelsee McDonough, Ryan Alba, Patria Halpin, Jared Singh, Vivekanand Yan, Yun Int J Pediatr Endocrinol Case Report BACKGROUND: Insulinoma is a rare diagnosis in the general population with estimates of 1 in 250,000 people per year. Reports of these pancreatic islet cell tumors are even more unusual in children and adolescents. Chronic hypoglycemia due to an insulinoma often presents with neuroglycopenic symptoms that can easily be overlooked, especially in adolescents where nonspecific complaints are common. This may result in delayed diagnosis with prolonged periods of untreated hypoglycemia and associated complications. The rarity of pediatric insulinoma, vagueness of presenting symptoms, and challenge of tumor localization make insulinoma a true diagnostic quandary for clinicians. CASE PRESENTATION: In this report, we present a 15-year-old female who visited her primary care provider complaining of intermittent episodes of altered mental status including fatigue, irritability, and poor concentration. Her outpatient management included routine laboratory studies, drug screening, electroencephalogram (EEG), valproic acid initiation, CT scan of the abdomen, and endoscopic ultrasound with documentation of hypoglycemia, but otherwise inconclusive results. The patient was admitted to a tertiary children’s hospital with severe refractory hypoglycemia 8 months after the initial evaluation. A serum critical sample was obtained and magnetic resonance imaging (MRI) of the abdomen performed which confirmed the presence of a pancreatic mass ultimately identified as an insulinoma. She went on to have surgical resection of her tumor resulting in complete resolution of her hypoglycemia and associated symptoms. CONCLUSION: Within this report we demonstrate the importance of being vigilant for fasting hypoglycemia secondary to insulinoma even when the patient presents with nonspecific symptoms such as fatigue, irritability, or problems with concentration. If these neuroglycopenic complaints are unnoticed or misdiagnosed, patients with a potentially curable disease are put at risk of neurologic injury, or even death, due to untreated severe hypoglycemia. BioMed Central 2016-07-29 2016 /pmc/articles/PMC4967349/ /pubmed/27478444 http://dx.doi.org/10.1186/s13633-016-0032-8 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Halpin, Kelsee
McDonough, Ryan
Alba, Patria
Halpin, Jared
Singh, Vivekanand
Yan, Yun
Vague neuroglycopenic complaints camouflage diagnosis of adolescent insulinoma: a case report
title Vague neuroglycopenic complaints camouflage diagnosis of adolescent insulinoma: a case report
title_full Vague neuroglycopenic complaints camouflage diagnosis of adolescent insulinoma: a case report
title_fullStr Vague neuroglycopenic complaints camouflage diagnosis of adolescent insulinoma: a case report
title_full_unstemmed Vague neuroglycopenic complaints camouflage diagnosis of adolescent insulinoma: a case report
title_short Vague neuroglycopenic complaints camouflage diagnosis of adolescent insulinoma: a case report
title_sort vague neuroglycopenic complaints camouflage diagnosis of adolescent insulinoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967349/
https://www.ncbi.nlm.nih.gov/pubmed/27478444
http://dx.doi.org/10.1186/s13633-016-0032-8
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