Osteoma and osteochondroma are both bone tumors in the body. Both are prone to occur in young and middle-aged people, and are also prone to occur in the dry ends of long tubular bones of the limbs, such as the proximal tibia, distal femur, and joints of the upper limbs. However, the difference between the two is very large. Osteosarcoma is generally a malignant tumor, and the pain is very severe. Generally, there will be night pain and rest pain. The lesion progresses very rapidly, and there may be some metastasis to internal organs. Generally, osteosarcoma patients do not survive long even after surgery, and the prognosis is very poor. However, osteochondroma is a common benign tumor, which is also seen in young and middle-aged people. However, this disease rarely causes pain. The local osteochondroma may grow larger before it is discovered. It is found that the local nodule may be larger, and then the osteochondroma will be discovered. Generally, the prognosis of osteochondroma is very good, and there are generally no pain symptoms. Generally, after surgical resection, it rarely recurs and will not metastasize. Therefore, there is still a clear difference between the two diseases. Chondrosarcoma and osteosarcoma are both common primary malignant tumors of bone. Chondrosarcoma is usually a low-grade malignant tumor characterized by the formation of cartilage matrix by malignant tumor cells. It is more common in adults, with a high incidence age of 30 to 60 years old. Osteosarcoma and chondrosarcoma are both malignant tumors of mesenchymal tissue, but their pathological types and tissue sources are completely different. Chondrosarcoma is caused by the malignant transformation of chondrocytes; What are the clinical manifestations of Ewing sarcoma? It often occurs in children and adolescents, and is highly malignant. It is most likely to occur at the epiphyseal end of long bones. The treatment is amputation plus radiotherapy and chemotherapy. The current treatment is a comprehensive treatment including radiotherapy and chemotherapy. In addition, surgery can increase the survival rate to more than 50%. There is significant tenderness, and the veins on the surface are distended. Sometimes the mass grows very fast in the soft tissue and can be as big as a human head within two to three months. Tumor masses occurring in the ilium can extend into the pelvis, and the mass can be felt in the lower abdomen and anus during examination. First of all, Ewing's sarcoma is a sarcoma with a relatively high degree of malignancy. Which department should I go to for osteosarcoma? Synovial sarcoma is a highly malignant soft tissue sarcoma that originates from mesenchymal cells with synovial differentiation. It is rarely found in joints, but is more likely to occur in the limbs and other parts of the body. Surface sarcomas may be skin fibromas or lipomas. A specific diagnosis requires removal of the surface tumor and then pathological examination. Patients with osteosarcoma generally need to go to the orthopedic department for relevant diagnosis and treatment. |
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