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Diffuse nesidioblastosis with hypoglycemia mimicking an insulinoma: a case report

INTRODUCTION: We describe a case of diffuse nesidioblastosis in an adult patient who presented with exclusively fasting symptoms and a focal pancreatic (111)In-pentetreotide uptake mimicking an insulinoma. CASE PRESENTATION: A 23-year-old Caucasian man had severe daily fasting hypoglycemia with gluc...

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Autores principales: Ferrario, Chiara, Stoll, Delphine, Boubaker, Ariane, Matter, Maurice, Yan, Pu, Puder, Jardena J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485087/
https://www.ncbi.nlm.nih.gov/pubmed/23031644
http://dx.doi.org/10.1186/1752-1947-6-332
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author Ferrario, Chiara
Stoll, Delphine
Boubaker, Ariane
Matter, Maurice
Yan, Pu
Puder, Jardena J
author_facet Ferrario, Chiara
Stoll, Delphine
Boubaker, Ariane
Matter, Maurice
Yan, Pu
Puder, Jardena J
author_sort Ferrario, Chiara
collection PubMed
description INTRODUCTION: We describe a case of diffuse nesidioblastosis in an adult patient who presented with exclusively fasting symptoms and a focal pancreatic (111)In-pentetreotide uptake mimicking an insulinoma. CASE PRESENTATION: A 23-year-old Caucasian man had severe daily fasting hypoglycemia with glucose levels below 2mmol/L. Besides rare neuroglycopenic symptoms (confusion, sleepiness), he was largely asymptomatic. His investigations revealed low venous plasma glucose levels, high insulin and C-peptide levels and a 72-hour fast test that were all highly suggestive for an insulinoma. Abdominal computed tomography and magnetic resonance imaging did not reveal any lesions. The sole imagery that was compatible with an insulinoma was a (111)In-somatostatin receptor scintigraphy that showed a faint but definite focal tracer between the head and the body of the pancreas. However, this lesion could not be confirmed by endoscopic ultrasonography of the pancreas. Following duodenopancreatectomy, the histological findings were consistent with diffuse nesidioblastosis. Postoperatively, the patient continued to present with fasting hypoglycemia and was successfully treated with diazoxide. CONCLUSION: In the absence of gastrointestinal surgery, nesidioblastosis is very rare in adults. In addition, nesidioblastosis is usually characterized by post-prandial hypoglycemia, whereas this patient presented with fasting hypoglycemia. This case also illustrates the risk for a false positive result of (111)In-pentetreotide scintigraphy in the case of nesidioblastosis. Selective arterial calcium stimulation and venous sampling is the most reliable procedure for the positive diagnosis of insulinoma or nesidioblastosis and should be used to confirm any suspicion based on imaging modalities.
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spelling pubmed-34850872012-11-01 Diffuse nesidioblastosis with hypoglycemia mimicking an insulinoma: a case report Ferrario, Chiara Stoll, Delphine Boubaker, Ariane Matter, Maurice Yan, Pu Puder, Jardena J J Med Case Rep Case Report INTRODUCTION: We describe a case of diffuse nesidioblastosis in an adult patient who presented with exclusively fasting symptoms and a focal pancreatic (111)In-pentetreotide uptake mimicking an insulinoma. CASE PRESENTATION: A 23-year-old Caucasian man had severe daily fasting hypoglycemia with glucose levels below 2mmol/L. Besides rare neuroglycopenic symptoms (confusion, sleepiness), he was largely asymptomatic. His investigations revealed low venous plasma glucose levels, high insulin and C-peptide levels and a 72-hour fast test that were all highly suggestive for an insulinoma. Abdominal computed tomography and magnetic resonance imaging did not reveal any lesions. The sole imagery that was compatible with an insulinoma was a (111)In-somatostatin receptor scintigraphy that showed a faint but definite focal tracer between the head and the body of the pancreas. However, this lesion could not be confirmed by endoscopic ultrasonography of the pancreas. Following duodenopancreatectomy, the histological findings were consistent with diffuse nesidioblastosis. Postoperatively, the patient continued to present with fasting hypoglycemia and was successfully treated with diazoxide. CONCLUSION: In the absence of gastrointestinal surgery, nesidioblastosis is very rare in adults. In addition, nesidioblastosis is usually characterized by post-prandial hypoglycemia, whereas this patient presented with fasting hypoglycemia. This case also illustrates the risk for a false positive result of (111)In-pentetreotide scintigraphy in the case of nesidioblastosis. Selective arterial calcium stimulation and venous sampling is the most reliable procedure for the positive diagnosis of insulinoma or nesidioblastosis and should be used to confirm any suspicion based on imaging modalities. BioMed Central 2012-10-02 /pmc/articles/PMC3485087/ /pubmed/23031644 http://dx.doi.org/10.1186/1752-1947-6-332 Text en Copyright ©2012 Ferrario et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ferrario, Chiara
Stoll, Delphine
Boubaker, Ariane
Matter, Maurice
Yan, Pu
Puder, Jardena J
Diffuse nesidioblastosis with hypoglycemia mimicking an insulinoma: a case report
title Diffuse nesidioblastosis with hypoglycemia mimicking an insulinoma: a case report
title_full Diffuse nesidioblastosis with hypoglycemia mimicking an insulinoma: a case report
title_fullStr Diffuse nesidioblastosis with hypoglycemia mimicking an insulinoma: a case report
title_full_unstemmed Diffuse nesidioblastosis with hypoglycemia mimicking an insulinoma: a case report
title_short Diffuse nesidioblastosis with hypoglycemia mimicking an insulinoma: a case report
title_sort diffuse nesidioblastosis with hypoglycemia mimicking an insulinoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485087/
https://www.ncbi.nlm.nih.gov/pubmed/23031644
http://dx.doi.org/10.1186/1752-1947-6-332
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