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A case report of insulinoma presenting with seizures and localized on endoscopic ultrasound
Insulinomas are rare functioning neuroendocrine (NEN) tumors. Up to 10% of insulinomas are associated with multiple endocrine neoplasia 1 (MEN1). Most of the tumors present with symptomatic hypoglycemia. Several non‐invasive and invasive techniques are used to localize the lesion. We present a case...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014521/ https://www.ncbi.nlm.nih.gov/pubmed/36937638 http://dx.doi.org/10.1002/ccr3.6967 |
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author | Umer, Waseem Mohammed, Ahmed Salah Khan, Adeel Ahmad Saddique, Muhammad Umar Zahid, Muhammad |
author_facet | Umer, Waseem Mohammed, Ahmed Salah Khan, Adeel Ahmad Saddique, Muhammad Umar Zahid, Muhammad |
author_sort | Umer, Waseem |
collection | PubMed |
description | Insulinomas are rare functioning neuroendocrine (NEN) tumors. Up to 10% of insulinomas are associated with multiple endocrine neoplasia 1 (MEN1). Most of the tumors present with symptomatic hypoglycemia. Several non‐invasive and invasive techniques are used to localize the lesion. We present a case of insulinoma presenting with seizure episodes with negative results on non‐invasive imaging diagnosed and localized with endoscopic ultrasound. A 36‐year‐old male was brought by ambulance to the emergency department with an episode of generalized tonic–clonic seizures. He had been previously healthy and did not have family history of neuro‐endocrine tumors. At the time of the attack, the patient's blood glucose checked via point‐of‐care testing was 28.8 (70–99 mg/dL). He was given IV dextrose. Physical examination after the patient regained consciousness was completely unremarkable. Hypoglycemia workup revealed a normal morning cortisol level of 281 (138–689 nmol/L). Insulin level was 62.4 mcunit/ml (2.36–24.9), and c‐peptide was 8.13 (1.1–4.4 ng/mL) consistent with hyperinsulinemia. Magnetic resonance cholangiopancreatography (MRCP), fluorine‐18‐l‐dihydroxyphenylalanine whole‐body positron emission tomography scan (NM 18F‐DOPA whole‐body PET scan), and gallium Ga 68 dodecanetetraacetic acid (Ga‐68 DOTATATE) scan were normal and did not reveal any pancreatic lesion consistent with insulinoma. Due to high suspicion of insulinoma and negative non‐invasive imaging, an endoscopic ultrasound (EUS) was performed, which showed a hypoechoic homogenous mass lesion sized 13 × 9 mm in the proximal body/neck of the pancreas. A fine needle biopsy (FNA) via EUS was performed. Histopathology showed a well‐differentiated neuroendocrine tumor, consistent with Grade 1 insulinoma (T1N0M0). The patient underwent a distal pancreatectomy and splenectomy. In cases of high clinical and biochemical suspicion of insulinoma but negative non‐invasive imaging, invasive modalities should be used to localize the culprit lesion. |
format | Online Article Text |
id | pubmed-10014521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100145212023-03-16 A case report of insulinoma presenting with seizures and localized on endoscopic ultrasound Umer, Waseem Mohammed, Ahmed Salah Khan, Adeel Ahmad Saddique, Muhammad Umar Zahid, Muhammad Clin Case Rep Case Report Insulinomas are rare functioning neuroendocrine (NEN) tumors. Up to 10% of insulinomas are associated with multiple endocrine neoplasia 1 (MEN1). Most of the tumors present with symptomatic hypoglycemia. Several non‐invasive and invasive techniques are used to localize the lesion. We present a case of insulinoma presenting with seizure episodes with negative results on non‐invasive imaging diagnosed and localized with endoscopic ultrasound. A 36‐year‐old male was brought by ambulance to the emergency department with an episode of generalized tonic–clonic seizures. He had been previously healthy and did not have family history of neuro‐endocrine tumors. At the time of the attack, the patient's blood glucose checked via point‐of‐care testing was 28.8 (70–99 mg/dL). He was given IV dextrose. Physical examination after the patient regained consciousness was completely unremarkable. Hypoglycemia workup revealed a normal morning cortisol level of 281 (138–689 nmol/L). Insulin level was 62.4 mcunit/ml (2.36–24.9), and c‐peptide was 8.13 (1.1–4.4 ng/mL) consistent with hyperinsulinemia. Magnetic resonance cholangiopancreatography (MRCP), fluorine‐18‐l‐dihydroxyphenylalanine whole‐body positron emission tomography scan (NM 18F‐DOPA whole‐body PET scan), and gallium Ga 68 dodecanetetraacetic acid (Ga‐68 DOTATATE) scan were normal and did not reveal any pancreatic lesion consistent with insulinoma. Due to high suspicion of insulinoma and negative non‐invasive imaging, an endoscopic ultrasound (EUS) was performed, which showed a hypoechoic homogenous mass lesion sized 13 × 9 mm in the proximal body/neck of the pancreas. A fine needle biopsy (FNA) via EUS was performed. Histopathology showed a well‐differentiated neuroendocrine tumor, consistent with Grade 1 insulinoma (T1N0M0). The patient underwent a distal pancreatectomy and splenectomy. In cases of high clinical and biochemical suspicion of insulinoma but negative non‐invasive imaging, invasive modalities should be used to localize the culprit lesion. John Wiley and Sons Inc. 2023-03-14 /pmc/articles/PMC10014521/ /pubmed/36937638 http://dx.doi.org/10.1002/ccr3.6967 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Report Umer, Waseem Mohammed, Ahmed Salah Khan, Adeel Ahmad Saddique, Muhammad Umar Zahid, Muhammad A case report of insulinoma presenting with seizures and localized on endoscopic ultrasound |
title | A case report of insulinoma presenting with seizures and localized on endoscopic ultrasound |
title_full | A case report of insulinoma presenting with seizures and localized on endoscopic ultrasound |
title_fullStr | A case report of insulinoma presenting with seizures and localized on endoscopic ultrasound |
title_full_unstemmed | A case report of insulinoma presenting with seizures and localized on endoscopic ultrasound |
title_short | A case report of insulinoma presenting with seizures and localized on endoscopic ultrasound |
title_sort | case report of insulinoma presenting with seizures and localized on endoscopic ultrasound |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014521/ https://www.ncbi.nlm.nih.gov/pubmed/36937638 http://dx.doi.org/10.1002/ccr3.6967 |
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