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Titlebook: Bone Tumors; Diagnosis and Therap Jaime Paulos,Dominique G. Poitout Book 2021 Springer-Verlag London Ltd., part of Springer Nature 2021 Bon

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發(fā)表于 2025-3-28 17:03:47 | 只看該作者
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發(fā)表于 2025-3-29 09:24:04 | 只看該作者
Osteochondroma and Hereditary Multiple Osteochondromashe remaining cases are part of the multiple hereditary osteochondromas syndrome. The pathogenesis is not entirely clear. Osteochondromas usually develop at the metaphysis of long bones. Malignant transformation is rare in solitary lesions, but more common in hereditary syndromes. Solitary osteochond
46#
發(fā)表于 2025-3-29 14:24:33 | 只看該作者
Enchondromaentally. Their clinical presentation can range from an asymptomatic lesion in an adult to multiple lesions as part of a syndrome in a younger patient. If the clinical and radiological presentation is characteristic, enchondromas can be treated non-operatively with observation alone. However, in cert
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發(fā)表于 2025-3-30 07:16:21 | 只看該作者
Ewing’s Sarcomaidence is low and all bones can be affected. Local pain and swelling are common signs of presentation. There are sometimes inflammatory signs such as fever and a macroscopic aspect looking like pus, thus mimicking infectious presentation. The presence of metastasis is high at the moment of the diagn
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