# Atypical Presentation of an Osteoid Osteoma With a Multicentric Nidus

**Authors:** Sandeep Kumar Thirlapuram, Khazi Syed Asif Hussain, Pragnya Keerthisree, Sundeep Kund Reddy Aluka

PMC · DOI: 10.7759/cureus.67053 · 2024-08-17

## TL;DR

A 12-year-old girl presented with a rare case of osteoid osteoma featuring two tumor centers, diagnosed through imaging and successfully treated with surgery.

## Contribution

This case report documents an atypical osteoid osteoma with a multicentric nidus in a young female, emphasizing the importance of imaging and surgical intervention.

## Key findings

- Osteoid osteoma with multicentric nidi was diagnosed in a 12-year-old girl using plain radiographs, CT, and MRI.
- Surgical excision was performed due to atypical presentation and lack of RFA experience for multicentric cases.
- The patient remained asymptomatic with no recurrence after six months of follow-up.

## Abstract

An osteoid osteoma is typically a benign bone tumor affecting young adult males, often presenting with nocturnal pain alleviated by nonsteroidal anti-inflammatory medications (NSAIDS). It usually manifests as a solitary nidus with surrounding sclerosis. An osteoid osteoma with a multicentric nidus, characterized by multiple nidi, is a rare variant. A 12-year-old girl presented with a one-year history of worsening, nighttime pain in her upper left leg. Plain radiographs revealed two lytic lesions with sclerosis. A computed tomography (CT) scan confirmed two well-defined sclerotic lesions with central lytic lesions. Magnetic resonance imaging (MRI) demonstrated two hypointense lesions with peripheral hyperintensity on short tau inversion recovery (STIR) sequences, suggestive of osteoid osteoma with a multicentric nidus. Differential diagnoses included osteomyelitis with Brodie's abscess, osteoblastoma, chondroblastoma, and malignant lesions. Due to the atypical presentation and lack of experience with radiofrequency ablation (RFA) for multicentric cases, surgical excision was performed. Histopathology confirmed osteoid osteoma. After rehabilitation, the patient was asymptomatic at six months with no recurrence on radiographs. This case highlights the unusual presentation of osteoid osteoma with a multicentric nidus in a young female. Radiological workup with plain films, CT, and MRI was crucial for diagnosis. While RFA is gaining popularity, surgical excision remains a valid option, especially for atypical cases.

## Linked entities

- **Diseases:** osteoid osteoma (MONDO:0009808), osteomyelitis (MONDO:0005246), osteoblastoma (MONDO:0018936), chondroblastoma (MONDO:0004997)

## Full-text entities

- **Diseases:** chondroblastoma (MESH:D002804), osteoblastoma (MESH:D018215), pain (MESH:D010146), osteomyelitis (MESH:D010019), benign (MESH:D009369), sclerosis (MESH:D012598), sclerotic lesions (MESH:C538213), Osteoid Osteoma (MESH:D010017), lytic lesions (MESH:D009059), bone tumor (MESH:D001859), Brodie's abscess (MESH:C536607)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11403376/full.md

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Source: https://tomesphere.com/paper/PMC11403376