Ewing's Sarcoma: Difference between revisions
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Ewing’s Sarcoma is a malignant primary tumor that can arise in soft tissue or bone. The pelvis and the lower extremities are the most common sites. <br> | Ewing’s Sarcoma is a malignant primary tumor that can arise in soft tissue or bone. The pelvis and the lower extremities are the most common sites. <br> | ||
== | Ewing's Sarcoma is the second most common primary malignant bone tumor of children and the fourth more common overall. 80% of these tumors occur in people under the age of 20 and they have been reported in children as young as 5 months. They rarely occur in the African American or Asian population.<sup>1,2</sup> == | ||
== Characteristics/Clinical Presentation == | == Characteristics/Clinical Presentation == |
Revision as of 06:01, 9 March 2011
Original Editors - Lisa Miville from Bellarmine University's Pathophysiology of Complex Patient Problems project.
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Definition/Description[edit | edit source]
Ewing’s Sarcoma is a malignant primary tumor that can arise in soft tissue or bone. The pelvis and the lower extremities are the most common sites.
Ewing's Sarcoma is the second most common primary malignant bone tumor of children and the fourth more common overall. 80% of these tumors occur in people under the age of 20 and they have been reported in children as young as 5 months. They rarely occur in the African American or Asian population.1,2 ==
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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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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Differential Diagnosis[edit | edit source]
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