Osteoblastoma

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Original Editors - Students from Bellarmine University's Pathophysiology of Complex Patient Problems project.

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Definition/Description[edit | edit source]

Osteoblastoma is a rare, benign osteoblastic (bone) tumor that most commonly develops in the spine, sacrum, long bones, and flat bones. Benign tumors do not spread to various sites or organs. However, an aggressive type of osteoblastoma has been identified in very rare occasions that have led to metastasis, death, and mimicked osteosarcoma. It is a bone tumor that histologically is very similar to that as an osteoid osteoma, which can make differentiating between the two difficult. Osteoblastoma tumors are typically larger, and have an osteolytic and sclerotic border when viewed on radiographs.

Prevalence[edit | edit source]

Of all benign bone tumors, osteoblastoma only accounts for about 1-2%, being more prevalent in males than females. This more commonly develops in men younger than 30, but can occur in ages as young as 2 and old as 70. Of those diagnosed with osteoblastoma, 80% of them are within the ages of 10 and 30.

Characteristics/Clinical Presentation[edit | edit source]

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Associated Co-morbidities[edit | edit source]

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Medications[edit | edit source]

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Diagnostic Tests/Lab Tests/Lab Values[edit | edit source]

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Etiology/Causes[edit | edit source]

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Systemic Involvement[edit | edit source]

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Medical Management (current best evidence)[edit | edit source]

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Physical Therapy Management (current best evidence)[edit | edit source]

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Alternative/Holistic Management (current best evidence)[edit | edit source]

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Differential Diagnosis[edit | edit source]

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Case Reports/ Case Studies[edit | edit source]

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Resources
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Recent Related Research (from Pubmed)[edit | edit source]

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References[edit | edit source]

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