Metastatic Insulinoma in a 16-Year-Old Adolescent Male With Men-1: A Case Report and Review of the Literature

ABSTRACT: Objective: Multiple endocrine neoplasia type 1 (MEN-1) is an autosomal dominant condition associated with various combinations of endocrine and nonendocrine tumors. Insulinomas are rare endocrine tumors in the pediatric age group and may be associated with MEN-1 in 10% of cases. Malignant...

Full description

Bibliographic Details
Main Authors: Ayse Pinar Cemeroglu, MD, Michael S. Racine, MD, Lora Kleis, RN, Heather Borders, MD, Beth A. Kurt, MD
Format: Article
Language:English
Published: Elsevier 2016-01-01
Series:AACE Clinical Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2376060520305988
id doaj-896d9023cdd4412ba1ddb87e0f8bec59
record_format Article
spelling doaj-896d9023cdd4412ba1ddb87e0f8bec592021-04-30T07:25:20ZengElsevierAACE Clinical Case Reports2376-06052016-01-0123e247e250Metastatic Insulinoma in a 16-Year-Old Adolescent Male With Men-1: A Case Report and Review of the LiteratureAyse Pinar Cemeroglu, MD0Michael S. Racine, MD1Lora Kleis, RN2Heather Borders, MD3Beth A. Kurt, MD4From the Helen DeVos Children's Hospital, Spectrum Health Medical Group, Pediatric Endocrinology, Grand Rapids, Michigan; Michigan State University, Grand Rapids Campus, Grand Rapids, Michigan; Address correspondence to Dr. Ayse Pinar Cemeroglu, Spectrum Health Medical Group, Helen DeVos Children's Hospital, 230 Michigan Street NE, Suite 101, MC 77, Grand Rapids, MI 49503.From the Helen DeVos Children's Hospital, Spectrum Health Medical Group, Pediatric Endocrinology, Grand Rapids, Michigan; Michigan State University, Grand Rapids Campus, Grand Rapids, MichiganFrom the Helen DeVos Children's Hospital, Spectrum Health Medical Group, Pediatric Endocrinology, Grand Rapids, MichiganSpectrum Health Advanced Radiology Services, Pediatric Radiology, Grand Rapids, MichiganMichigan State University, Grand Rapids Campus, Grand Rapids, Michigan; Helen DeVos Children's Hospital, Spectrum Health Medical Group, Pediatric Hematology and Oncology, Grand Rapids, Michigan.ABSTRACT: Objective: Multiple endocrine neoplasia type 1 (MEN-1) is an autosomal dominant condition associated with various combinations of endocrine and nonendocrine tumors. Insulinomas are rare endocrine tumors in the pediatric age group and may be associated with MEN-1 in 10% of cases. Malignant insulinomas only constitute 5 to 10% of all the insulinomas and are exceedingly rare in children. There are only 11 cases of malignant insulinoma reported in the literature in the pediatric age group.Methods: We are reporting a 16-year-old adolescent male who presented with symptoms of hypoglycemia for the 4 months prior to referral.Results: He was diagnosed with malignant insulinoma with multiple metastases to liver and was treated with surgical resection followed by octreotide treatment. He had additional findings consistent with the diagnosis of MEN-1, including elevated prolactin levels combined with a 4 to 5 mm pituitary lesion possibly due to prolactinoma and mildly elevated calcium levels with a parathyroid ultrasound demonstrating a parathyroid adenoma on the left side measuring 8 × 6 × 4 mm in diameter. He has been free of symptoms and radiologic findings of recurrence of insulinoma 1-year post surgery.Conclusion: Malignant insulinoma is extremely rare in children, but should be considered in cases of hyperinsulinemic hypoglycemia. MEN-1 should also be considered because insulinoma may be the first finding of MEN-1. Surgical resection is the treatment of choice. Somatostatin analog is a safe and effective treatment in children in cases with metastatic insulinoma when residual tumor is present.Abbreviations: MEN-1 = multiple endocrine neoplasia-1 MRI = magnetic resonance imaginghttp://www.sciencedirect.com/science/article/pii/S2376060520305988
collection DOAJ
language English
format Article
sources DOAJ
author Ayse Pinar Cemeroglu, MD
Michael S. Racine, MD
Lora Kleis, RN
Heather Borders, MD
Beth A. Kurt, MD
spellingShingle Ayse Pinar Cemeroglu, MD
Michael S. Racine, MD
Lora Kleis, RN
Heather Borders, MD
Beth A. Kurt, MD
Metastatic Insulinoma in a 16-Year-Old Adolescent Male With Men-1: A Case Report and Review of the Literature
AACE Clinical Case Reports
author_facet Ayse Pinar Cemeroglu, MD
Michael S. Racine, MD
Lora Kleis, RN
Heather Borders, MD
Beth A. Kurt, MD
author_sort Ayse Pinar Cemeroglu, MD
title Metastatic Insulinoma in a 16-Year-Old Adolescent Male With Men-1: A Case Report and Review of the Literature
title_short Metastatic Insulinoma in a 16-Year-Old Adolescent Male With Men-1: A Case Report and Review of the Literature
title_full Metastatic Insulinoma in a 16-Year-Old Adolescent Male With Men-1: A Case Report and Review of the Literature
title_fullStr Metastatic Insulinoma in a 16-Year-Old Adolescent Male With Men-1: A Case Report and Review of the Literature
title_full_unstemmed Metastatic Insulinoma in a 16-Year-Old Adolescent Male With Men-1: A Case Report and Review of the Literature
title_sort metastatic insulinoma in a 16-year-old adolescent male with men-1: a case report and review of the literature
publisher Elsevier
series AACE Clinical Case Reports
issn 2376-0605
publishDate 2016-01-01
description ABSTRACT: Objective: Multiple endocrine neoplasia type 1 (MEN-1) is an autosomal dominant condition associated with various combinations of endocrine and nonendocrine tumors. Insulinomas are rare endocrine tumors in the pediatric age group and may be associated with MEN-1 in 10% of cases. Malignant insulinomas only constitute 5 to 10% of all the insulinomas and are exceedingly rare in children. There are only 11 cases of malignant insulinoma reported in the literature in the pediatric age group.Methods: We are reporting a 16-year-old adolescent male who presented with symptoms of hypoglycemia for the 4 months prior to referral.Results: He was diagnosed with malignant insulinoma with multiple metastases to liver and was treated with surgical resection followed by octreotide treatment. He had additional findings consistent with the diagnosis of MEN-1, including elevated prolactin levels combined with a 4 to 5 mm pituitary lesion possibly due to prolactinoma and mildly elevated calcium levels with a parathyroid ultrasound demonstrating a parathyroid adenoma on the left side measuring 8 × 6 × 4 mm in diameter. He has been free of symptoms and radiologic findings of recurrence of insulinoma 1-year post surgery.Conclusion: Malignant insulinoma is extremely rare in children, but should be considered in cases of hyperinsulinemic hypoglycemia. MEN-1 should also be considered because insulinoma may be the first finding of MEN-1. Surgical resection is the treatment of choice. Somatostatin analog is a safe and effective treatment in children in cases with metastatic insulinoma when residual tumor is present.Abbreviations: MEN-1 = multiple endocrine neoplasia-1 MRI = magnetic resonance imaging
url http://www.sciencedirect.com/science/article/pii/S2376060520305988
work_keys_str_mv AT aysepinarcemeroglumd metastaticinsulinomaina16yearoldadolescentmalewithmen1acasereportandreviewoftheliterature
AT michaelsracinemd metastaticinsulinomaina16yearoldadolescentmalewithmen1acasereportandreviewoftheliterature
AT lorakleisrn metastaticinsulinomaina16yearoldadolescentmalewithmen1acasereportandreviewoftheliterature
AT heatherbordersmd metastaticinsulinomaina16yearoldadolescentmalewithmen1acasereportandreviewoftheliterature
AT bethakurtmd metastaticinsulinomaina16yearoldadolescentmalewithmen1acasereportandreviewoftheliterature
_version_ 1721498341135613952