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Nesidioblastosis and Insulinoma: A Rare Coexistence and a Therapeutic Challenge

Background: Nesidioblastosis and insulinoma are disorders of the endocrine pancreas causing endogenous hyperinsulinemic hypoglycemia. Their coexistence is very unusual and treatment represents a still unresolved dilemma. Case Description: The patient was a 43-year-old Caucasian woman, with a 2-year...

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Autores principales: Dardano, Angela, Daniele, Giuseppe, Lupi, Roberto, Napoli, Niccolò, Campani, Daniela, Boggi, Ugo, Del Prato, Stefano, Miccoli, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996476/
https://www.ncbi.nlm.nih.gov/pubmed/32047477
http://dx.doi.org/10.3389/fendo.2020.00010
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author Dardano, Angela
Daniele, Giuseppe
Lupi, Roberto
Napoli, Niccolò
Campani, Daniela
Boggi, Ugo
Del Prato, Stefano
Miccoli, Roberto
author_facet Dardano, Angela
Daniele, Giuseppe
Lupi, Roberto
Napoli, Niccolò
Campani, Daniela
Boggi, Ugo
Del Prato, Stefano
Miccoli, Roberto
author_sort Dardano, Angela
collection PubMed
description Background: Nesidioblastosis and insulinoma are disorders of the endocrine pancreas causing endogenous hyperinsulinemic hypoglycemia. Their coexistence is very unusual and treatment represents a still unresolved dilemma. Case Description: The patient was a 43-year-old Caucasian woman, with a 2-year history of repeated severe hypoglycemic events. The diagnostic work-up was strongly suggestive of insulinoma and the patient was submitted to surgical treatment carried out laparoscopically under robotic assistance. However, surgical exploration and intraoperative ultrasonography failed to detect a pancreatic tumor. Resection was therefore carried out based on the results of selective intra-arterial calcium stimulation test, following a step-up approach, eventually leading to a pancreatoduodenectomy at the splenic artery. The histopathology examination and the immunohistochemical staining were consistent with adult-onset nesidioblastosis. After surgery, the patient continued to experience hypoglycemia with futile response to medical treatments (octreotide, calcium antagonists, diazoxide, and prednisone). Following multidisciplinary evaluation and critical review of a repeat abdominal computed tomography scan, a small nodular lesion was identified in the tail of the pancreas. The nodule was enucleated laparoscopically and the pathological examination revealed an insulinoma. In spite of the insulinoma resection, glycemic values were only partially restored, with residual nocturnal hypoglycemia. Administration of uncooked cornstarch (1.25 g/kg body weight) at bedtime was associated with significant improvement of interstitial glucose levels (p < 0.0001) and reduction of nocturnal hypoglycemia episodes (p = 0.0002). Conclusions: This report describes a rare coexistence of adult-onset nesidioblastosis and insulinoma, suggesting the existence of a wide and continuous spectrum of proliferative β-cell changes. Moreover, we propose that uncooked cornstarch may offer an additional approach to alleviate the hypoglycemic episodes when surgery is impracticable/unaccepted.
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spelling pubmed-69964762020-02-11 Nesidioblastosis and Insulinoma: A Rare Coexistence and a Therapeutic Challenge Dardano, Angela Daniele, Giuseppe Lupi, Roberto Napoli, Niccolò Campani, Daniela Boggi, Ugo Del Prato, Stefano Miccoli, Roberto Front Endocrinol (Lausanne) Endocrinology Background: Nesidioblastosis and insulinoma are disorders of the endocrine pancreas causing endogenous hyperinsulinemic hypoglycemia. Their coexistence is very unusual and treatment represents a still unresolved dilemma. Case Description: The patient was a 43-year-old Caucasian woman, with a 2-year history of repeated severe hypoglycemic events. The diagnostic work-up was strongly suggestive of insulinoma and the patient was submitted to surgical treatment carried out laparoscopically under robotic assistance. However, surgical exploration and intraoperative ultrasonography failed to detect a pancreatic tumor. Resection was therefore carried out based on the results of selective intra-arterial calcium stimulation test, following a step-up approach, eventually leading to a pancreatoduodenectomy at the splenic artery. The histopathology examination and the immunohistochemical staining were consistent with adult-onset nesidioblastosis. After surgery, the patient continued to experience hypoglycemia with futile response to medical treatments (octreotide, calcium antagonists, diazoxide, and prednisone). Following multidisciplinary evaluation and critical review of a repeat abdominal computed tomography scan, a small nodular lesion was identified in the tail of the pancreas. The nodule was enucleated laparoscopically and the pathological examination revealed an insulinoma. In spite of the insulinoma resection, glycemic values were only partially restored, with residual nocturnal hypoglycemia. Administration of uncooked cornstarch (1.25 g/kg body weight) at bedtime was associated with significant improvement of interstitial glucose levels (p < 0.0001) and reduction of nocturnal hypoglycemia episodes (p = 0.0002). Conclusions: This report describes a rare coexistence of adult-onset nesidioblastosis and insulinoma, suggesting the existence of a wide and continuous spectrum of proliferative β-cell changes. Moreover, we propose that uncooked cornstarch may offer an additional approach to alleviate the hypoglycemic episodes when surgery is impracticable/unaccepted. Frontiers Media S.A. 2020-01-24 /pmc/articles/PMC6996476/ /pubmed/32047477 http://dx.doi.org/10.3389/fendo.2020.00010 Text en Copyright © 2020 Dardano, Daniele, Lupi, Napoli, Campani, Boggi, Del Prato and Miccoli. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Dardano, Angela
Daniele, Giuseppe
Lupi, Roberto
Napoli, Niccolò
Campani, Daniela
Boggi, Ugo
Del Prato, Stefano
Miccoli, Roberto
Nesidioblastosis and Insulinoma: A Rare Coexistence and a Therapeutic Challenge
title Nesidioblastosis and Insulinoma: A Rare Coexistence and a Therapeutic Challenge
title_full Nesidioblastosis and Insulinoma: A Rare Coexistence and a Therapeutic Challenge
title_fullStr Nesidioblastosis and Insulinoma: A Rare Coexistence and a Therapeutic Challenge
title_full_unstemmed Nesidioblastosis and Insulinoma: A Rare Coexistence and a Therapeutic Challenge
title_short Nesidioblastosis and Insulinoma: A Rare Coexistence and a Therapeutic Challenge
title_sort nesidioblastosis and insulinoma: a rare coexistence and a therapeutic challenge
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996476/
https://www.ncbi.nlm.nih.gov/pubmed/32047477
http://dx.doi.org/10.3389/fendo.2020.00010
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