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The Oncologist, ISSN 1083-7159, 02/2014, Volume 19, Issue 2, pp. 193 - 201
Learning Objectives Explain the characteristics and treatment of malignant peripheral nerve sheath tumors, both in relation to neurofibromatosis type I and... 
Clinical trials | Molecular targeted therapy | Neurofibromatosis type 1 | Sarcoma | Malignant peripheral nerve sheath tumor | MAMMALIAN TARGET | NEUROFIBROMATOSIS TYPE-I | PHASE-II | SOFT-TISSUE | MPNST | GENE | ONCOLOGY | SARCOMA | NF1 | INHIBITOR | TYPE-1 | Animals | Nerve Sheath Neoplasms - therapy | Humans | Nerve Sheath Neoplasms - pathology | Nerve Sheath Neoplasms - diagnosis | Sarcomas
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 05/2015, Volume 39, Issue 5, pp. 673 - 682
Epithelioid malignant peripheral nerve sheath tumor (EMPNST) is rare and differs from conventional malignant peripheral nerve sheath tumor by showing diffuse... 
epithelioid | sarcoma | soft tissue | malignant peripheral nerve sheath tumor | INI1 | SURGERY | SERIES | RARE | PATHOLOGY | SOFT-TISSUE | VARIANT | BENIGN ANCIENT SCHWANNOMA | EWSR1 GENE | PATIENT | SPECTRUM | OF-THE-LITERATURE | Immunohistochemistry | Biomarkers, Tumor - analysis | Humans | Middle Aged | Male | Neurilemmoma - pathology | Young Adult | Adolescent | Aged, 80 and over | Adult | Female | Aged | Child | Epithelioid Cells - pathology
Journal Article
Medicine, ISSN 0025-7974, 01/2019, Volume 98, Issue 4, p. e14223
Rationale: Malignant peripheral nerve sheath tumors (MPNSTs) are rare neoplasms with only a few reported cases affecting the nasal cavity, paranasal sinuses,... 
HEAD | MEDICINE, GENERAL & INTERNAL | malignant peripheral nerve sheath tumour | EXPERIENCE | NECK | nasopharynx | nasal cavity mass | pediatric | Nose Neoplasms - pathology | Humans | Nasal Cavity | Nerve Sheath Neoplasms - pathology | Female | Child | Nasopharyngeal Neoplasms - pathology | Case studies | Nose cancer | Tumors in children | Care and treatment | Diagnosis
Journal Article
Advances in Experimental Medicine and Biology, ISSN 0065-2598, 2016, Volume 916, pp. 495 - 530
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 10/2019, Volume 43, Issue 10, pp. 1323 - 1330
Spindle cell rhabdomyosarcoma (RMS) is an aggressive sarcoma type with a predilection for the head and neck and frequent transactivating MYOD1 mutations.... 
H3K27 TRIMETHYLATION LOSS | SUZ12 | SURGERY | DIAGNOSIS | METHYLATION | malignant peripheral nerve sheath tumor | PRC2 | MARKER | immunohistochemistry | MUTATIONS | PATHOLOGY | spindle cell rhabdomyosarcoma | Diagnosis, Differential | Nervous system tumors | Rhabdomyosarcoma | Physiological aspects | Genetic aspects | Diagnosis | Peripheral nerve diseases | Methods
Journal Article