# Acute Encephalopathy and Severe Hypercalcemia as the Initial Presentation of a Large Parathyroid Hormone-Related Protein (PTHrP)-Secreting Pancreatic Neuroendocrine Tumor: A Case Report

**Authors:** Katherine M Collamore, Parul Jandir, Jennifer Hashem, Alejandro Cruz Ponce, Michael Levitt

PMC · DOI: 10.7759/cureus.92717 · Cureus · 2025-09-19

## TL;DR

A rare pancreatic tumor caused severe hypercalcemia and brain issues, showing how early diagnosis can improve outcomes.

## Contribution

Highlights a rare initial presentation of a PTHrP-secreting pNET causing acute encephalopathy and severe hypercalcemia.

## Key findings

- A 15 cm pancreatic tumor was found to secrete PTHrP, leading to severe hypercalcemia.
- Neurologic symptoms improved after treating hypercalcemia with hydration, calcitonin, zoledronic acid, and dialysis.
- Lanreotide therapy was initiated for managing the neuroendocrine tumor.

## Abstract

Pancreatic neuroendocrine tumors (pNETs) are rare neoplasms that present with diverse clinical manifestations depending on their secretory activity. Paraneoplastic hypercalcemia due to parathyroid hormone-related peptide (PTHrP) secretion by pNETs is an uncommon but serious complication. We describe the case of a 67-year-old female with a past medical history of multiple sclerosis and uveitis presenting with acute metabolic encephalopathy due to profound hypercalcemia. Laboratory workup revealed a corrected calcium of 22.4 mg/dL and PTHrP of 327 pg/mL. Imaging demonstrated a new 15 cm pancreatic mass with adrenal nodules suspicious for metastatic disease. Pathology from a percutaneous biopsy confirmed a well-differentiated pNET with a Ki-67 index of ~15%. The patient’s mental status improved following treatment of hypercalcemia with intravenous hydration, calcitonin, zoledronic acid, and urgent hemodialysis. She was started on lanreotide therapy for pNET treatment. This case highlights the importance of considering pNETs in the differential diagnosis of unexplained hypercalcemia, as timely recognition and management can reverse neurologic dysfunction and improve outcomes. Awareness of this rare presentation may facilitate earlier diagnosis and treatment of underlying neuroendocrine malignancies.

## Linked entities

- **Proteins:** PTHLH (parathyroid hormone like hormone)
- **Chemicals:** calcitonin (PubChem CID 118984394), zoledronic acid (PubChem CID 68740)
- **Diseases:** multiple sclerosis (MONDO:0005301), uveitis (MONDO:0020283), hypercalcemia (MONDO:0001566), encephalopathy (MONDO:0005560), pancreatic neuroendocrine tumor (MONDO:0019954), pNET (MONDO:0005462)

## Full-text entities

- **Genes:** PTHLH (parathyroid hormone like hormone) [NCBI Gene 5744] {aka BDE2, HHM, PLP, PTHR, PTHRP}
- **Diseases:** multiple sclerosis (MESH:D009103), pancreatic mass (MESH:D010195), Hypercalcemia (MESH:D006934), Encephalopathy (MESH:D001927), adrenal nodules (MESH:D016606), neoplasms (MESH:D009369), uveitis (MESH:D014605), neurologic dysfunction (MESH:D009461), metabolic encephalopathy (MESH:D001928), disease (MESH:D004194), Pancreatic Neuroendocrine Tumor (MESH:D018358), pNET (MESH:D018242)
- **Chemicals:** zoledronic acid (MESH:D000077211), calcium (MESH:D002118)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12535749/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12535749/full.md

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Source: https://tomesphere.com/paper/PMC12535749