# Cavernous Hemangioma: A Rare Adrenal Tumor Associated With Hyperaldosteronism

**Authors:** Hannah Sage, Edward Jones, Vladimir Neychev

PMC · DOI: 10.7759/cureus.79251 · Cureus · 2025-02-18

## TL;DR

A rare adrenal tumor called cavernous hemangioma was found to cause high aldosterone levels in a patient with uncontrolled hypertension.

## Contribution

This case highlights cavernous hemangioma as a potential cause of hyperaldosteronism in adrenal masses.

## Key findings

- The patient had a 5 cm adrenal mass associated with hyperaldosteronism, not pheochromocytoma.
- Surgical pathology confirmed the mass was a cavernous hemangioma with no malignancy.
- Post-surgery, the patient's blood pressure and aldosterone levels normalized.

## Abstract

Adrenal cavernous hemangiomas are rare benign venous malformations characterized by vascular dysmorphogenesis. A 53-year-old male patient was referred for a surgical consultation with a 5 cm heterogeneous, lipid-poor, incidental left adrenal mass. It was detected on a computed tomography (CT) scan performed for left upper quadrant pain. His past medical history was significant for poorly-controlled hypertension on a multi-drug regimen, anxiety, headaches, insomnia, and palpitations. Laboratory testing performed by his primary care physician revealed elevated plasma catecholamines, which were concerning for pheochromocytoma. A repeat workup by endocrinology and endocrine surgery showed biochemical evidence of primary hyperaldosteronism with an aldosterone/plasma renin ratio of 36.8 and normal plasma catecholamines and metanephrines. Due to the biochemical workup, size, and radiological features of the mass, a decision to proceed with a left adrenalectomy was made. The patient was started on phenoxybenzamine two weeks before surgery due to a high index of clinical suspicion for a pheochromocytoma, despite the equivocal biochemical workup. Surgical pathology revealed a cavernous hemangioma with pseudonodular thickening of the adrenal cortex without evidence of malignancy, adrenal adenoma, or pheochromocytoma. On follow-up, the patient was on fewer antihypertensive medications with normal blood pressure and a normalized aldosterone/plasma renin ratio. A diagnosis of cavernous hemangioma should be considered for adrenal masses of uncertain biology and biochemical activity.

## Linked entities

- **Chemicals:** phenoxybenzamine (PubChem CID 4768)
- **Diseases:** hyperaldosteronism (MONDO:0003009), pheochromocytoma (MONDO:0004974), anxiety (MONDO:0005618), insomnia (MONDO:0013600)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}
- **Diseases:** Adrenal Tumor (MESH:D000310), headaches (MESH:D006261), pheochromocytoma (MESH:D010673), venous malformations (MESH:C563977), adrenal mass (MESH:C536030), pain (MESH:D010146), Adrenal cavernous hemangiomas (MESH:D006392), anxiety (MESH:D001007), insomnia (MESH:D007319), palpitations (MESH:D006331), malignancy (MESH:D009369), Hyperaldosteronism (MESH:D006929), hypertension (MESH:D006973), adrenal adenoma (MESH:D018246)
- **Chemicals:** aldosterone (MESH:D000450), lipid (MESH:D008055), phenoxybenzamine (MESH:D010643), metanephrines (MESH:D008676), catecholamines (MESH:D002395)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC11929149/full.md

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Source: https://tomesphere.com/paper/PMC11929149