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  • Chordoma - Symptoms and causes - Mayo Clinic
    Overview Chordoma is a rare type of bone cancer that starts as a growth of cells in the bones of the spine or the skull It most often forms where the skull sits atop the spine, called the skull base, or at the bottom of the spine, called the sacrum
  • Chordoma: What It Is, Types, Symptoms Treatment - Cleveland Clinic
    Chordoma is a rare bone tumor that forms in your spine or skull base All subtypes of chordoma are considered cancerous (malignant) Surgical removal of the tumor is the first-line treatment, but it can be difficult to completely remove chordomas due to their location near your spinal cord or brainstem
  • Chordoma - Wikipedia
    Chordoma is a rare slow-growing neoplasm (cancer) that arises from cellular remnants of the notochord in the bones of the skull base and spine The evidence for the notochordal origin of chordoma is the location of the tumors (along the neuraxis), the similar immunohistochemical staining patterns, expression of brachyury, and the demonstration that notochordal cells are preferentially left
  • Chordoma - NCI - National Cancer Institute
    Chordoma is a slow growing cancer of tissue found inside the spine Chordoma can happen anywhere along the spine It is most often found near the tailbone (called a sacral tumor) or where the spine meets the skull (called a clival tumor)
  • Understanding chordoma - Chordoma Foundation
    Our glossary of commonly used terms can help you understand the medical and scientific terms you may hear when discussing your diagnosis with your care team ; Stacchiotti S, Sommer J, Chordoma Global Consensus Group Building a global consensus approach to chordoma: a position paper from the medical and patient community Lancet Oncology 2015 Feb;16(2):e71-83 doi: 10 1016 S1470-2045(14)71190-8
  • Chordoma: Rare Cancer in Spine and Skull - WebMD
    Chordoma is a kind of cancer that grows in the bones of your skull and spine It's very rare Only 1 out of every 1 million people gets it About 300 people are diagnosed with chordoma in the
  • Pathology Outlines - Chordoma
    Malignant tumor with notochordal differentiation 3 types: Conventional chordoma: ~95% of cases; chondroid chordoma is a subtype of conventional chordoma (World Neurosurg 2017;104:346) Poorly differentiated chordoma (very rare): cohesive sheets of epithelioid cells with eosinophilic cytoplasm and loss of INI1 staining; positive for brachyury
  • Q A: Chordoma, a one in a million bone cancer - MD Anderson Cancer Center
    When you have a rare cancer that only affects one in a million people, it can be difficult to find the answers and information you need That’s why we sat down with spinal neurosurgeon Laurence Rhines, M D , and skull base neurosurgeon Shaan Raza, M D , to discuss chordoma, a rare, malignant tumor diagnosed in about 300 people each year in the United States


















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