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Giant insulinoma in a 15-year-old man: A case report

INTRODUCTION: Giant insulinomas are extremely rare pancreatic neuroendocrine tumor. PRESENTATION OF CASE: A 15-year-old man presenting with acute onset of lightheadedness was found to have serum glucose of 1.5 mmol/L. The blood collected from the hypoglycemic episode showed an inappropriately high i...

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Autores principales: Vasikasin, Vasin, Watthanatham, Jirawat, Napatharatip, Prateep, Termmathurapoj, Sumeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899312/
https://www.ncbi.nlm.nih.gov/pubmed/27258815
http://dx.doi.org/10.1016/j.ijscr.2016.05.037
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author Vasikasin, Vasin
Watthanatham, Jirawat
Napatharatip, Prateep
Termmathurapoj, Sumeth
author_facet Vasikasin, Vasin
Watthanatham, Jirawat
Napatharatip, Prateep
Termmathurapoj, Sumeth
author_sort Vasikasin, Vasin
collection PubMed
description INTRODUCTION: Giant insulinomas are extremely rare pancreatic neuroendocrine tumor. PRESENTATION OF CASE: A 15-year-old man presenting with acute onset of lightheadedness was found to have serum glucose of 1.5 mmol/L. The blood collected from the hypoglycemic episode showed an inappropriately high insulin and C-peptide level. Abdominal computerized tomography showed a 12.5 cm well-defined, lobulated hypervascular mass at pancreatic tail, without any evidence of metastasis. En bloc resection with distal pancreatectomy, and splenectomy was successfully performed. The pathological examination confirmed insulinoma, with benign characteristics. Follow-up after the procedure revealed neither hypoglycemic, nor hyperglycemia. CONCLUSION: We report the youngest case of a giant insulinoma. Despite the size of the tumor, the pathological report confirmed the benign characteristics. However, long-term follow-up is still essential to detect recurrence in the future.
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spelling pubmed-48993122016-06-21 Giant insulinoma in a 15-year-old man: A case report Vasikasin, Vasin Watthanatham, Jirawat Napatharatip, Prateep Termmathurapoj, Sumeth Int J Surg Case Rep Case Report INTRODUCTION: Giant insulinomas are extremely rare pancreatic neuroendocrine tumor. PRESENTATION OF CASE: A 15-year-old man presenting with acute onset of lightheadedness was found to have serum glucose of 1.5 mmol/L. The blood collected from the hypoglycemic episode showed an inappropriately high insulin and C-peptide level. Abdominal computerized tomography showed a 12.5 cm well-defined, lobulated hypervascular mass at pancreatic tail, without any evidence of metastasis. En bloc resection with distal pancreatectomy, and splenectomy was successfully performed. The pathological examination confirmed insulinoma, with benign characteristics. Follow-up after the procedure revealed neither hypoglycemic, nor hyperglycemia. CONCLUSION: We report the youngest case of a giant insulinoma. Despite the size of the tumor, the pathological report confirmed the benign characteristics. However, long-term follow-up is still essential to detect recurrence in the future. Elsevier 2016-05-25 /pmc/articles/PMC4899312/ /pubmed/27258815 http://dx.doi.org/10.1016/j.ijscr.2016.05.037 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Vasikasin, Vasin
Watthanatham, Jirawat
Napatharatip, Prateep
Termmathurapoj, Sumeth
Giant insulinoma in a 15-year-old man: A case report
title Giant insulinoma in a 15-year-old man: A case report
title_full Giant insulinoma in a 15-year-old man: A case report
title_fullStr Giant insulinoma in a 15-year-old man: A case report
title_full_unstemmed Giant insulinoma in a 15-year-old man: A case report
title_short Giant insulinoma in a 15-year-old man: A case report
title_sort giant insulinoma in a 15-year-old man: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899312/
https://www.ncbi.nlm.nih.gov/pubmed/27258815
http://dx.doi.org/10.1016/j.ijscr.2016.05.037
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