Atypical Presentation of an Osteoid Osteoma With a Multicentric Nidus
Sandeep Kumar Thirlapuram, Khazi Syed Asif Hussain, Pragnya Keerthisree, Sundeep Kund Reddy Aluka

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.
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,…
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Taxonomy
TopicsBone Tumor Diagnosis and Treatments · Sarcoma Diagnosis and Treatment · Cancer-related molecular mechanisms research
