Results 151 to 160 of about 5,276 (179)
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Radiotherapy and Oncology, 2019
Malignant peripheral nerve sheath tumors (MPNST) may be sporadic or associated with neurofibromatosis or prior radiation. MPNST may behave aggressively with a high rate of local recurrence and distant metastasis.In an IRB approved protocol, we reviewed the clinical characteristics, treatment, and outcomes of 280 patients treated for MPNST at ...
Ruoyu Miao +12 more
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Malignant peripheral nerve sheath tumors (MPNST) may be sporadic or associated with neurofibromatosis or prior radiation. MPNST may behave aggressively with a high rate of local recurrence and distant metastasis.In an IRB approved protocol, we reviewed the clinical characteristics, treatment, and outcomes of 280 patients treated for MPNST at ...
Ruoyu Miao +12 more
openaire +2 more sources
Journal of Clinical Oncology, 2011
10066 Background: Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder associated with several clinical manifestations, including peripheral neurofibromas. Malignant transformation of these neurofibromas into malignant peripheral nerve sheath tumors (MPNST) is a potential life-threatening sequelae of this syndrome.
K. N. Johnson +5 more
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10066 Background: Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder associated with several clinical manifestations, including peripheral neurofibromas. Malignant transformation of these neurofibromas into malignant peripheral nerve sheath tumors (MPNST) is a potential life-threatening sequelae of this syndrome.
K. N. Johnson +5 more
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Malignant Peripheral Nerve Sheath Tumor (MPNST)
1999This usually high-grade sarcoma mainly consists of spindle cells of both schwannian and fibroblastic type, and occasionally may have focal heterogeneous differentiation, such as chondroid, osteoid, rhabdomyoblastic, epithelial, endothelial, and melanocytic. This histology recapitulates the components of the nerve sheath (Schwann cells and fibroblasts),
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TRPS1 expression in MPNST is correlated with PRC2 inactivation and loss of H3K27me3
Human PathologyInitially described as a highly specific immunohistochemical marker for carcinomas of mammary origin, trichorhinophalangeal syndrome type 1 (TRPS1) has subsequently been detected in a variety of other non-mammary tumors. In this study, we examined the immunohistochemical expression of TRPS1 in 114 peripheral nerve sheath tumors, including 43 malignant ...
Rossana Lazcano +5 more
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Stem-like cells drive NF1-associated MPNST functional heterogeneity and tumor progression
Cell Stem Cell, 2021Jack Shern +2 more
exaly
Surgical strategies and the use of functional reconstructions after resection of MPNST
Orthoplastic Surgery, 2021Cornelis Verhoef +2 more
exaly
COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF MPNST
2022HAO HUAIXIANG +3 more
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