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The way concept relations are shown:
The way concept relations are shown:
Neurofibrosarcoma
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate concepts∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate concepts∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Neurofibrosarcoma 7 coordinate conceptsX |
Broader terms: | |
Annotation: | coord IM with precoord organ/neopl term (IM)
X |
History note: | |
historyNote*: | 94
X |
publicMeSHNote*: | 94
X |
Scope note: | 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)
X |
activeMeSHYear*: | |
dateCreated*: | 1993-06-25X |
dateEstablished*: | 1994-01-01X |
dateRevised*: | 1999-11-03X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | KEVX |
recordOriginator*: | PLSX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Neurofibrosarkooma (fi) XNeurofibrosarkom (sv) Sarcoma, Neurogenic (en, replaced) Neurofibrosarcoma (la-FI, replaced) |
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