# A Case of Pancreatic Metastasis of Renal Cancer Coexisting With a Pancreatic Neuroendocrine Tumor in a Patient Diagnosed With Fulminant Type 1 Diabetes Mellitus

**Authors:** Kento Miyazaki, Masaharu Ishida, Masahiro Iseki, Masamichi Mizuma, Michiaki Unno

PMC · DOI: 10.7759/cureus.79489 · 2025-02-23

## TL;DR

A rare case is reported where a patient developed fulminant type 1 diabetes alongside a pancreatic tumor and metastasis from a previous kidney cancer.

## Contribution

This case highlights a rare coexistence of fulminant type 1 diabetes with pancreatic neuroendocrine tumor and metastatic renal cancer.

## Key findings

- A 72-year-old man had F1DM, PanNET, and pancreatic metastasis from renal cancer without chemotherapy or viral infection.
- Pathological analysis confirmed metastatic renal cell carcinoma and neuroendocrine tumors in the pancreas.
- Post-surgery, the patient's insulin requirement decreased significantly.

## Abstract

Fulminant type 1 diabetes mellitus (F1DM) is a subtype of type 1 diabetes that typically arises from viral infections or exposure to anticancer drugs. In the absence of these triggers, F1DM rarely develops concurrently with pancreatic tumors. This report presents a unique case of F1DM occurring alongside a pancreatic neuroendocrine tumor (PanNET) and pancreatic metastasis of renal cancer. A 72-year-old man with a history of right nephrectomy for renal cancer 20 years prior presented with a sudden onset of severe thirst. Laboratory investigations revealed hyperglycemia, ketoacidosis, and depleted insulin levels, leading to a diagnosis of F1DM. Abdominal computed tomography imaging identified multiple, rapidly enhancing tumors within the pancreatic body and tail, suggestive of metastatic renal cancer. The patient underwent a distal pancreatectomy and splenectomy. Pathological examination confirmed the presence of metastatic renal cell carcinoma and neuroendocrine tumors within the pancreas. A significant reduction in the number of pancreatic islets was observed, and the remaining islets exhibited a complete absence of insulin production. The postoperative course was uneventful, with a notable decrease in the required insulin dosage by approximately 50%. We experienced a rare case of PanNET and pancreatic metastasis of renal cancer complicated with F1DM, in the absence of chemotherapy or viral infection. The possibility of a coexisting pancreatic tumor should be considered in cases of fulminant type 1 diabetes.

## Linked entities

- **Diseases:** type 1 diabetes (MONDO:0005147), renal cancer (MONDO:0005206), pancreatic neuroendocrine tumor (MONDO:0019954)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** viral infection (MESH:D014777), tumors (MESH:D009369), hyperglycemia (MESH:D006943), F1DM (MESH:D003922), renal cancer (MESH:D007680), PanNET (MESH:D018358), renal cell carcinoma (MESH:D002292), ketoacidosis (MESH:D007662), Pancreatic Metastasis of Renal Cancer (MESH:D010190)
- **Chemicals:** anticancer (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11934003/full.md

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Source: https://tomesphere.com/paper/PMC11934003