# From Secondary Hyperparathyroidism to Neurologic Crisis: A Tale of Brown Tumor and Spinal Cord Compression

**Authors:** Aryn Kormanis, Matthew Anderson, Miya McKnight, Hima Darapu

PMC · DOI: 10.1210/jcemcr/luaf022 · JCEM Case Reports · 2025-03-20

## TL;DR

A patient with a rare brown tumor in the spine caused neurological issues, requiring surgery to relieve spinal cord compression.

## Contribution

Highlights the rare occurrence of brown tumors in the thoracic spine causing neurological symptoms and the need for surgical decompression.

## Key findings

- A brown tumor at T4-T5 caused severe spinal canal stenosis and right lower extremity weakness.
- Subtotal parathyroidectomy significantly reduced parathyroid hormone levels during surgery.
- Surgical decompression was necessary to address neurological deficits caused by the tumor.

## Abstract

A 26-year-old male with medical history of polycystic kidney disease, IgA nephropathy, end-stage renal disease, and brown tumor (requiring prior surgical intervention on brown tumor) was hospitalized because of right lower extremity weakness. Examination revealed right hip flexor weakness and right foot clonus. Laboratory results showed serum calcium of 10.4 mg/dL (2.59 mmol/L) (reference range: 8.5-10.5 mg/dL; 2.12-2.62 mmol/L). Magnetic resonance imaging displayed a 2.5 × 3.7 cm soft tissue mass with circumferential encroachment of the epidural space leading to severe spinal canal stenosis of T4-T5 at the site of prior brown tumor resection. The patient underwent subtotal parathyroidectomy with left cervical thymectomy, leading to an intraoperative PTH drop from >3500 pg/mL (>371 pmol/L) (reference range: 12-88 pg/mL; 1.27-9.33 pmol/L) to 247 pg/mL (26.182 pmol/L). In the context of treating vertebral brown tumors, the consensus suggests that parathyroidectomy plays a crucial role in achieving both clinical and radiographical amelioration of the tumor. However, in cases like ours where paresis is present, surgical decompression of the tumor becomes imperative. The development of brown tumors is an uncommon and severe, long-term complication for hyperparathyroidism. The location of a brown tumor in the thoracic spine causing symptomatic cord compression is rare.

## Linked entities

- **Diseases:** polycystic kidney disease (MONDO:0020642), IgA nephropathy (MONDO:0005342), end-stage renal disease (MONDO:0004375), hyperparathyroidism (MONDO:0001741)

## Full-text entities

- **Genes:** PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}
- **Diseases:** hyperparathyroidism (MESH:D006961), foot clonus (MESH:D005530), paresis (MESH:D010291), spinal canal stenosis (MESH:D013130), Cord Compression (MESH:D013117), Neurologic Crisis (MESH:D009461), Brown Tumor (MESH:D009369), hip flexor weakness (MESH:D018908), Secondary Hyperparathyroidism (MESH:D006962), end-stage renal disease (MESH:D007676), lower extremity weakness (MESH:D020335), IgA nephropathy (MESH:D005922), polycystic kidney disease (MESH:D007690)
- **Chemicals:** calcium (MESH:D002118)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC11924185/full.md

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Source: https://tomesphere.com/paper/PMC11924185