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Related Concept Videos

Type I Diabetes III: Clinical Manifestations01:19

Type I Diabetes III: Clinical Manifestations

Type 1 diabetes mellitus typically presents with rapid-onset symptoms due to the body’s inability to utilize glucose in the absence of insulin. Since insulin is required for glucose uptake into cells, its deficiency leads to hyperglycemia and cellular energy deprivation, resulting in characteristic clinical features.Polyuria and PolydipsiaOne of the earliest, most prominent symptoms is polyuria (excessive urination). When blood glucose concentrations rise above the renal threshold, the kidneys...
Type I Diabetes I: Introduction01:12

Type I Diabetes I: Introduction

Type 1 diabetes mellitus is a chronic metabolic disorder characterized by an absolute deficiency of insulin resulting from the autoimmune destruction of pancreatic β-cells. Although it can occur at any age, it is most commonly diagnosed in childhood, adolescence, or early adulthood. The loss of insulin production impairs cellular glucose uptake, resulting in persistent hyperglycemia and necessitating lifelong insulin therapy.Autoimmune Destruction of β-CellsThe hallmark of type 1 diabetes is an...
Type I Diabetes II: Pathophysiology01:26

Type I Diabetes II: Pathophysiology

Type 1 diabetes mellitus arises from an immune-mediated destruction of pancreatic β-cells, resulting in an absolute deficiency of insulin. This process develops in genetically susceptible individuals when autoimmunity, environmental exposures, and immunologic dysregulation converge to trigger a targeted attack on the insulin-producing cells of the pancreas. The β-cells are located within the islets of Langerhans and are essential for regulating blood glucose by facilitating cellular uptake of...
Diabetes Mellitus: Introduction01:26

Diabetes Mellitus: Introduction

Diabetes mellitus consists of chronic metabolic disorders characterized by persistent hyperglycemia. This elevated blood glucose results from defects in insulin secretion, impaired insulin action, or both. Insulin, produced by pancreatic β-cells, is essential for maintaining glucose homeostasis by facilitating cellular glucose uptake for energy or storage. Disruptions in insulin production or function lead to glucose accumulation in the bloodstream, causing the clinical features and long-term...
Diabetes Mellitus: Overview and Type I Subtype01:22

Diabetes Mellitus: Overview and Type I Subtype

Diabetes mellitus is a chronic metabolic disorder characterized by high blood glucose levels due to inadequate insulin production, insulin resistance, or both. The condition affects millions worldwide and can significantly impact their health and quality of life.
Type 1 diabetes is an autoimmune disease in which the immune system mistakenly attacks and destroys the insulin-producing beta cells in the pancreas. As a result, the body is unable to produce sufficient insulin, and individuals with...
Type II Diabetes I: Introduction01:26

Type II Diabetes I: Introduction

Type 2 diabetes mellitus (T2DM) is a chronic metabolic disorder characterized by insulin resistance, in which target tissues such as the liver, muscle, and adipose tissue respond poorly to insulin. It is also associated with inadequate compensatory insulin secretion, where pancreatic β-cells fail to produce sufficient insulin. Together, these abnormalities lead to persistent hyperglycemia.EtiologyT2DM develops through a complex interaction of genetic predisposition and environmental or...

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Related Experiment Video

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Robotic Enucleation of an Intra-Pancreatic Insulinoma in the Pancreatic Head
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Published on: January 3, 2020

[Malignant insulinoma].

Miklós Tóth1, Nikolette Szücs, Zsuzsa Jakab

  • 1Semmelweis Egyetem, Általános Orvostudományi Kar, II. Belgyógyászati Klinika, Budapest. totmik@bel2.sote.hu

Orvosi Hetilap
|March 1, 2011
PubMed
Summary
This summary is machine-generated.

This case study details a metastatic neuroendocrine carcinoma of the pancreas. Despite treatment, the patient developed hypoglycemia due to insulin oversecretion, highlighting challenges in managing advanced neuroendocrine tumors.

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Last Updated: Jun 4, 2026

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Published on: January 3, 2020

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Published on: April 17, 2026

Area of Science:

  • Oncology
  • Endocrinology
  • Nuclear Medicine

Background:

  • Neuroendocrine tumors (NETs) are neoplasms originating from neuroendocrine cells.
  • Pancreatic NETs (PNETs) can exhibit aggressive behavior and metastasize.
  • Metastatic PNETs pose significant management challenges, particularly when associated with hormonal syndromes.

Observation:

  • A 56-year-old man presented with epigastric pain, found to have a pancreatic head tumor with liver metastasis.
  • Pathology revealed moderately differentiated neuroendocrine carcinoma with moderate proliferative activity (Ki-67).
  • Initial treatment with chemotherapy, interferon, and somatostatin analogue showed limited efficacy against rapidly progressing metastatic disease.

Findings:

  • Octreotide scintigraphy confirmed high somatostatin receptor expression on both primary and metastatic lesions.
  • ⁹⁰Yttrium-DOTATOC peptide receptor radionuclide therapy (PRRT) yielded a mixed response over three sessions.
  • Late-stage disease progression led to severe hypoglycemia due to insulin oversecretion, confirmed by elevated insulin and C-peptide levels.
  • Diazoxide was poorly tolerated; chemoembolization provided only temporary relief.

Implications:

  • This case underscores the complex management of advanced, metastatic pancreatic neuroendocrine carcinoma.
  • Effective control of hormonal syndromes, such as hypoglycemia, is critical in advanced NETs.
  • PRRT can be a therapeutic option for somatostatin receptor-positive metastatic NETs, but outcomes can be variable.
  • Multimodality treatment approaches are often necessary for advanced neuroendocrine neoplasms.