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...
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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 |
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