scholarly journals Characterization of Peripheral Nerve Sheath Tumors with 3T Proton MR Spectroscopy

2013 ◽  
Vol 35 (5) ◽  
pp. 1035-1041 ◽  
Author(s):  
L. M. Fayad ◽  
X. Wang ◽  
J. O. Blakeley ◽  
D. J. Durand ◽  
M. A. Jacobs ◽  
...  
Keyword(s):  
Peripheral Nerve ◽  
Mr Spectroscopy ◽  
Proton Mr Spectroscopy ◽  
Nerve Sheath Tumors ◽  
Peripheral Nerve Sheath Tumors ◽  
Nerve Sheath

scholarly journals GENE-26. MOLECULAR CHARACTERIZATION OF BENIGN AND MALIGNANT PERIPHERAL NERVE SHEATH TUMORS THAT OCCUR IN SPORADIC AND SYNDROMIC SETTINGS

2018 ◽  
Vol 20 (suppl_6) ◽  
pp. vi108-vi109
Author(s):  
Suganth Suppiah ◽  
Shirin Karimi ◽  
Sheila Mansouri ◽  
Yasin Mamatjan ◽  
Jeff Liu ◽  
...  
Keyword(s):  
Peripheral Nerve ◽  
Molecular Characterization ◽  
Nerve Sheath Tumors ◽  
Peripheral Nerve Sheath Tumors ◽  
Nerve Sheath

scholarly journals Establishment and characterization of patient-derived cancer models of malignant peripheral nerve sheath tumors

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Rieko Oyama ◽  
Fusako Kito ◽  
Mami Takahashi ◽  
Emi Hattori ◽  
Rei Noguchi ◽  
...  
Keyword(s):  
Peripheral Nerve ◽  
Nerve Sheath Tumors ◽  
Peripheral Nerve Sheath Tumors ◽  
Nerve Sheath ◽  
Cancer Models

scholarly journals Malignant Peripheral Nerve Sheath Tumors—A Comprehensive Review of Pathophysiology, Diagnosis, and Multidisciplinary Management

Children ◽  
2022 ◽  
Vol 9 (1) ◽  
pp. 38
Author(s):  
Samantha W. E. Knight ◽  
Tristan E. Knight ◽  
Teresa Santiago ◽  
Andrew J. Murphy ◽  
Abdelhafeez H. Abdelhafeez
Keyword(s):  
Peripheral Nerve ◽  
Relevant Literature ◽  
Soft Tissue Sarcomas ◽  
Neurofibromatosis Type ◽  
Comprehensive Review ◽  
Nerve Sheath Tumors ◽  
Peripheral Nerve Sheath Tumors ◽  
Nerve Sheath ◽  
Medical Oncologists

Malignant peripheral nerve sheath tumors (MPNSTs) are aggressive soft tissue sarcomas (STS) with nerve sheath differentiation and a tendency to metastasize. Although occurring at an incidence of 0.001% in the general population, they are relatively common in individuals with neurofibromatosis type 1 (NF1), for whom the lifetime risk approaches 10%. The staging of MPNSTs is complicated and requires close multi-disciplinary collaboration. Their primary management is most often surgical in nature, with non-surgical modalities playing a supportive, necessary role, particularly in metastatic, invasive, or widespread disease. We, therefore, sought to provide a comprehensive review of the relevant literature describing the characteristics of these tumors, their pathophysiology and risk factors, their diagnosis, and their multi-disciplinary treatment. A close partnership between surgical and medical oncologists is therefore necessary. Advances in the molecular characterization of these tumors have also begun to allow the integration of targeted RAS/RAF/MEK/ERK pathway inhibitors into MPNST management.

scholarly journals Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine

2015 ◽  
Vol 7 (5) ◽  
pp. 608-627 ◽  
Author(s):  
Joan Castellsagué ◽  
Bernat Gel ◽  
Juana Fernández‐Rodríguez ◽  
Roger Llatjós ◽  
Ignacio Blanco ◽  
...  
Keyword(s):  
Personalized Medicine ◽  
Peripheral Nerve ◽  
Mouse Models ◽  
Nerve Sheath Tumors ◽  
Peripheral Nerve Sheath Tumors ◽  
Nerve Sheath

Cytogenetic characterization of six malignant peripheral nerve sheath tumors

2001 ◽  
Vol 128 (1) ◽  
pp. 14-23 ◽  
Author(s):  
Hannelore Schmidt ◽  
Helge Taubert ◽  
Peter Würl ◽  
Matthias Bache ◽  
Frank Bartel ◽  
...  
Keyword(s):  
Peripheral Nerve ◽  
Nerve Sheath Tumors ◽  
Peripheral Nerve Sheath Tumors ◽  
Nerve Sheath ◽  
Cytogenetic Characterization
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