# A Giant Pediatric Ossifying Fibroma: A Case Report of a Rare Occipital Presentation

**Authors:** Ramón Castruita Meza, Oswaldo M Soriano, Glaucia B Tola Tarqui, Samuel García Torres, Vicente González Carranza

PMC · DOI: 10.7759/cureus.101980 · Cureus · 2026-01-21

## TL;DR

A rare case of a large ossifying fibroma in a child's occipital bone was successfully treated with surgery, improving vision and highlighting the need for early diagnosis.

## Contribution

This is the fifth reported case of a pediatric ossifying fibroma in the occipital region, emphasizing its rare presentation and management.

## Key findings

- A nine-year-old girl had a large occipital ossifying fibroma confirmed by histopathology.
- Surgical removal led to improved vision and reduced brain compression.
- This case highlights the importance of considering rare bone tumors in pediatric differential diagnoses.

## Abstract

Ossifying fibroma is a very uncommon tumor that affects craniofacial structures. Occipital bone presentation is extremely rare; it is more commonly found in the jaw. Its locally aggressive behavior and expansion near brain tissue require total surgical removal.

We report a nine-year-old girl with a five-year history of a growing, painless mass in the occipital region of the skull and progressive loss of vision. In the imaging studies, an extra-axial mass arising from the occipital bone was identified, with significant compression of the brain parenchyma. An occipital craniectomy and complete en bloc resection were performed, with histopathology confirming ossifying fibroma. Improvement in vision after surgery was noted. To our knowledge, this is the fifth reported case and is complemented by a review of the literature. The uncommon presentation of bone tumors, such as ossifying fibroma, with locally aggressive behavior should always be considered in the differential diagnosis in the pediatric population, because total resection decreases morbidity and can be curative.

## Linked entities

- **Diseases:** ossifying fibroma (MONDO:0002119)

## Full-text entities

- **Genes:** GNAS (GNAS complex locus) [NCBI Gene 2778] {aka AHO, AIMAH1, C20orf45, GNAS1, GPSA, GSA}
- **Diseases:** swelling (MESH:D004487), craniofacial fibro-osseous lesions (MESH:D000070896), weakness (MESH:D018908), benign neoplasms (MESH:D009369), occipital (MESH:D006259), pain (MESH:D010146), blurred vision (MESH:D014786), bone tumors (MESH:D001859), Fibrous dysplasia (MESH:D005357), cemento-ossifying fibroma (MESH:D002485), papilledema (MESH:D010211), headache (MESH:D006261), osteolytic (MESH:D030981), Painless mass (MESH:C536030), neurological deficit (MESH:D009461), VI nerve palsy (MESH:D020434), calvarial lesions (MESH:C537963), numbness (MESH:D006987), cranial trauma (MESH:D020197), brain injury (MESH:D001930), lesions of the mandible (MESH:C563485), diplopia (MESH:D004172), hyperostosis (MESH:D015576), Coma (MESH:D003128), benign lesions of the nervous system (MESH:D009422), posterior fossa lesion (MESH:D015192), dural tears (MESH:D020785), Ossifying Fibroma (MESH:D018214), intracranial hypertension (MESH:D019586), embolization (MESH:D004617)
- **Chemicals:** eosin (MESH:D004801), gadolinium (MESH:D005682)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC12922460/full.md

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Source: https://tomesphere.com/paper/PMC12922460