# Unexpected Paraganglioma Identified During Bilateral Nephrectomy in Autosomal Dominant Polycystic Kidney Disease: A Case Report

**Authors:** Mehdi Vollet, Catherine Blanc, Maurice Matter, Gregory Hofmann

PMC · DOI: 10.7759/cureus.92464 · Cureus · 2025-09-16

## TL;DR

A patient with kidney disease had unexpected tumors discovered during surgery, highlighting the need for thorough checks in similar cases.

## Contribution

Highlights the importance of considering paragangliomas in ADPKD patients with severe hypertension.

## Key findings

- A 6.3-cm paraganglioma was discovered during surgery in a patient with ADPKD.
- A 13-cm metastasis of myxoid liposarcoma and a second 0.4-cm paraganglioma were identified.
- Perioperative hemodynamic instability occurred but resolved without organ failure.

## Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is commonly associated with hypertension, which is typically attributed to renal dysfunction. However, secondary causes of hypertension, particularly pheochromocytomas and paragangliomas (PPGLs), should be considered in cases of severe or difficult-to-control hypertension.

We report the case of a 77-year-old woman with ADPKD and end-stage renal disease who underwent bilateral nephrectomy before kidney transplantation. Despite requiring four antihypertensive medications, her hypertension was attributed to renal disease. During left nephrectomy, manipulation of a perirenal mass resulted in a severe hypertensive crisis followed by refractory hypotension. Intraoperative frozen section analysis revealed an unsuspected 6.3-cm paraganglioma, while final pathology further demonstrated a 13-cm perirenal metastasis of the previously known myxoid liposarcoma, and also identified a second 0.4-cm peri-aortic paraganglioma.

The patient experienced significant perioperative hemodynamic instability but recovered without organ failure. Postoperative complications included arteriovenous fistula occlusion, which was successfully managed. The discovery of metastatic disease led to reassessment of transplant candidacy.

This case highlights the importance of considering PPGLs in ADPKD patients with severe hypertension requiring multiple antihypertensive medications. Preoperative biochemical screening and appropriate perioperative management are crucial for patient safety. The complexity of imaging interpretation in ADPKD patients requires careful multidisciplinary evaluation to exclude neoplastic processes.

## Linked entities

- **Diseases:** Autosomal dominant polycystic kidney disease (MONDO:0004691), paragangliomas (MONDO:0000448), myxoid liposarcoma (MONDO:0013280)

## Full-text entities

- **Diseases:** end-stage renal disease (MESH:D007676), Paraganglioma (MESH:D010235), myxoid liposarcoma (MESH:D018208), ADPKD (MESH:D016891), organ failure (MESH:D009102), hypotension (MESH:D007022), renal disease (MESH:D007674), metastatic disease (MESH:D000092182), PPGLs (MESH:D010673), metastasis (MESH:D009362), arteriovenous fistula occlusion (MESH:D001164), hypertension (MESH:D006973)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12530456/full.md

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Source: https://tomesphere.com/paper/PMC12530456