MeSH 搜索器

Neurofibrosarcoma

A malignant tumor that arises from small cutaneous nerves, is locally aggressive, and has a potential for metastasis. Characteristic histopathologic features include proliferating atypical spindle cells with slender wavy and pointed nuclei, hypocellular areas, and areas featuring organized whorls of fibroblastic proliferation. The most common primary sites are the extremities, retroperitoneum, and trunk. These tumors tend to present in childhood, often in association with NEUROFIBROMATOSIS 1. (From DeVita et al., Cancer: Principles & Practice of Oncology, 5th ed, p1662; Mayo Clin Proc 1990 Feb;65(2):164-72)
推出的年份: 1994
副标题
树号: C04.557.450.565.590.350.590, C04.557.450.795.350.590, C04.557.580.600.580.795, C10.551.775.500.750.750, C10.668.829.725.500.600.600
MeSH 单一 ID: D018319
进入的组:
  • Neurofibrosarcomas
  • Sarcoma, Neurogenic
  • Neurogenic Sarcoma
  • Neurogenic Sarcomas
  • Sarcomas, Neurogenic
  • Malignant Peripheral Nerve Sheath Tumors
  • Neurilemmosarcoma
  • Neurilemmosarcomas
  • MPNST
  • Malignant Neurilemmoma
  • Malignant Neurilemmomas
  • Neurilemmoma, Malignant
  • Peripheral Nerve Sheath Tumors, Malignant
  • Malignant Neurilemoma
  • Malignant Neurilemomas
  • Neurilemoma, Malignant
  • Schwannoma, Malignant
  • Malignant Schwannoma
  • Malignant Schwannomas
  • Malignant Peripheral Nerve Sheath Tumor
早前的内容:
  • Fibrosarcoma (1966-1978)
  • Neurofibroma (1969-1993)

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