sarcoma
Research Topic
Language: English
This is a research topic created to provide authors with a place to attach new problem publications.
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- The overall survival rate of osteosarcoma (OS) patients has not been improved for 30 years, and the diagnosis and treatment of OS is still a critical issue.
- Rhabdomyosarcoma (RMS) is a malignant soft tissue sarcoma of childhood including two major histological subtypes, alveolar (ARMS) and embryonal (ERMS) RMS.
- Adrenal sarcomas are rare malignant tumors with structural and clinical similarities to sarcomatoid adrenocortical carcinoma.
- Myeloid sarcoma is a rare extramedullary tumor of immature myeloid cells.
- Ewing sarcoma is a bone and soft tissue sarcoma that occurs in children and young adults.
- Ewing's sarcoma is a malignant tumor, with an extremely aggressive growth pattern and a high risk of metastasis.
- Response to neoadjuvant chemotherapy is a significant prognostic factor for osteosarcoma (OS) and the Ewing sarcoma family of tumors (ESFT).