# Giant Cell Tumor of the Sacrum With Secondary Changes of an Aneurysmal Bone Cyst: A Case Report

**Authors:** Akanksha Kalwaghe, Suresh Phatak, Kajal Mitra, Prashant Onkar, Sagar Gund

PMC · DOI: 10.7759/cureus.101356 · Cureus · 2026-01-12

## TL;DR

A 21-year-old woman with a rare sacral giant cell tumor and aneurysmal bone cyst changes is reported, emphasizing the need for accurate diagnosis and timely treatment.

## Contribution

This case report adds to the limited literature on sacral giant cell tumors with secondary aneurysmal bone cyst transformation.

## Key findings

- Imaging showed a well-defined, expansile osteolytic lesion with features of GCT and fluid-fluid levels consistent with aneurysmal bone cyst changes.
- Histopathology confirmed the diagnosis of GCT with secondary aneurysmal bone cyst transformation.
- Surgical excision and preoperative embolization were key in managing this rare and aggressive tumor.

## Abstract

Giant cell tumor (GCT) of bone is a typically benign but locally aggressive neoplasm that occurs between the ages of 20 and 40 years, and most commonly arises in the epiphysis of long bones, with sacral involvement being rare and diagnostically challenging due to its insidious onset and nonspecific symptoms. We report the case of a 21-year-old woman who presented with progressive low back pain radiating to both lower limbs, associated with perianal numbness and bilateral heel pain aggravated by physical activity. Imaging revealed a well-defined, expansile osteolytic lesion involving the S1-S2 vertebrae with features suggestive of a GCT. Magnetic resonance imaging (MRI) demonstrated an avidly enhancing mass extending into the spinal canal, causing compression of the thecal sac and adjacent nerve roots, more pronounced on the right side, along with fluid-fluid levels consistent with secondary aneurysmal bone cyst-like changes. Histopathological examination confirmed the diagnosis of GCT with secondary aneurysmal bone cyst transformation. Sacral GCTs are rare, locally aggressive lesions that often present with neurological symptoms, and imaging typically shows an expansile “soap-bubble” osteolytic lesion with possible soft-tissue extension and secondary cystic changes. Surgical excision remains the mainstay of treatment, with preoperative transarterial embolization playing an important role in reducing tumor vascularity and intraoperative blood loss. This case highlights the importance of including GCT in the differential diagnosis of sacral lesions in young adults and underscores the role of timely imaging and biopsy in establishing an accurate diagnosis and guiding appropriate management.

## Linked entities

- **Diseases:** Giant cell tumor (MONDO:0002171), Aneurysmal bone cyst (MONDO:0018815)

## Full-text entities

- **Diseases:** osteolytic lesion (MESH:D030981), low back pain (MESH:D017116), GCT (MESH:D005870), Sacral GCTs (MESH:C537221), blood (MESH:D006402), neoplasm (MESH:D009369), numbness (MESH:D006987), heel pain (MESH:D010146), Aneurysmal Bone Cyst (MESH:D017824)
- **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/PMC12893187/full.md

## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12893187/full.md

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Source: https://tomesphere.com/paper/PMC12893187