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Neurofibrosarcoma

Known as: Neurogenic Sarcomas, Neurofibrosarcomas, neurosarcomas 
A malignant tumor that arises from small cutaneous nerves, is locally aggressive, and has a potential for metastasis. Characteristic histopathologic… Expand
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
BACKGROUND Patients affected by neurofibromatosis type 1 (NF1) are at higher risk of developing soft-tissue sarcomas (STS) than… Expand
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Highly Cited
1999
Highly Cited
1999
Neurogenic sarcomas are incurable, common malignant human peripheral nerve tumors subject to local recurrence and systemic… Expand
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Highly Cited
1994
Highly Cited
1994
We studied 43 patients with ganglioneuromas of the gastrointestinal tract accessioned at the Armed Forces Institute of Pathology… Expand
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Highly Cited
1993
Highly Cited
1993
Individuals with neurofibromatosis type 1 (NF1) have an increased risk of developing benign and malignant tumours. The NF1 gene… Expand
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Highly Cited
1992
Highly Cited
1992
DEFECTS in the NF1 gene have been implicated in the inherited disorder neurofibromatosis type 1, which is characterized by… Expand
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Highly Cited
1992
Highly Cited
1992
Seventy-five primary sarcomas of the heart were classified by histologic appearance as angiosarcoma (26 cases), undifferentiated… Expand
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Highly Cited
1990
Highly Cited
1990
von Recklinghausen neurofibromatosis (NF1) is a common hereditary disorder characterized by neural crest-derived tumors… Expand
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Highly Cited
1988
Highly Cited
1988
Tumor grade is currently the most important factor in the staging of patients with soft tissue sarcomas. In previous studies, a… Expand
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Highly Cited
1982
Highly Cited
1982
ABSTRACTThe presence of S-100 protein was immunohistochemically studied in many types of formalin-fixed and paraffin-embedded… Expand
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