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peripheral chondrosarcoma. There are also exceedingly rare descriptions of periosteal Ewing sarcoma. 5 Regarding clinical symptoms, these are non-specific and include pain, local swelling and limited range of motion of the adjacent joint. Pain is usually
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to pain, pathological fractures, immobility, decreased functioning, and hypercalcaemia. Over half of patients experience clinical symptoms for which treatment is required, 3 of whom only a minority are surgically treated. 4 In the long bones
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bone. In the past, mostly palliative treatments, radiotherapy and pain relief were favoured. Nowadays, modern diagnostic tools (PET-CT, whole body MRI, etc) are included in the follow-up protocols allowing for early detection of bony metastases. Besides
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years after the diagnosis of a primary neoplasm or at the same presentation. The treatment of a metastatic bone lesion has multiple goals that must be achieved, such as reducing pain, restoring functionality, or maintaining functionality without the
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-mechanical rest pain, soft tissue swelling, change in size of the mass, fever, night sweats and chills, which would warrant a higher level of suspicion for malignancy. 4 Diagnostic imaging is an important component of the workup of a patient with a
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Clinical symptoms may differ based on location and phase of MO. Patients usually present with pain, swelling, oedema in superficial lesions and joint stiffness (up to 20% of patients). Pain generally persists longer than would be expected in a simple injury
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history. Current symptoms of malaise, fevers or unremitting pain, especially at night, should ring alarm bells for neoplasia. The pain of primary bone tumours and metastatic bone disease is similar. Initially, a deep-seated dull pain can be intermittent
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all bone tumors ( 1 ). ABCs occur in children or adolescents with a mean age of 13 years old, and most of the lesions appear before the age of 30 years ( 8 , 9 ). Common symptoms and signs observed with this lesion are pain, swelling, deformity, and
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females (1:1.5) and a very low incidence – 10.2 per million/year for L-TGCT and 4.1 per million/year in the D-TGCT type. 2 , 4 Patients with TGCT most commonly present with non-specific symptoms such as pain, repeated non-traumatic joint effusions
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enchondroma from a low-grade chondrosarcoma. The presence of focal pain is often used to crudely distinguish a chondrosarcoma, but it may be difficult to localize pain in the paediatric population. In a study based on initial clinical and imaging information