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Quoted phrase not found in phrase index: "Unresectable Malignant Peripheral Nerve Sheath Tumor"
Page 1
Epithelioid malignant peripheral nerve sheath tumor: clinicopathologic analysis of 63 cases.
Jo VY, Fletcher CD. Jo VY, et al. Am J Surg Pathol. 2015 May;39(5):673-82. doi: 10.1097/PAS.0000000000000379. Am J Surg Pathol. 2015. PMID: 25602794
Epithelioid malignant peripheral nerve sheath tumor (EMPNST) is rare and differs from conventional malignant peripheral nerve sheath tumor by showing diffuse S-100 protein positivity, infrequent association wit …
Epithelioid malignant peripheral nerve sheath tumor (EMPNST) is rare and differs from conventional mal …
Functional imaging of RAS pathway targeting in malignant peripheral nerve sheath tumor cells and xenografts.
Butler E, Schwettmann B, Geboers S, Hao G, Kim J, Nham K, Sun X, Laetsch TW, Xu L, Williams NS, Skapek SX. Butler E, et al. Pediatr Blood Cancer. 2020 Dec;67(12):e28639. doi: 10.1002/pbc.28639. Epub 2020 Sep 25. Pediatr Blood Cancer. 2020. PMID: 32975370
BACKGROUND: Malignant peripheral nerve sheath tumor (MPNST) is an aggressive form of soft-tissue sarcoma (STS) in children. ...CONCLUSION: The ability of MEK inhibitors to control MPNST growth cannot simply be predicted by serum drug leve …
BACKGROUND: Malignant peripheral nerve sheath tumor (MPNST) is an aggressive form of soft-tissue sarcoma …
Unusual primary tumors of the heart.
Vander Salm TJ. Vander Salm TJ. Semin Thorac Cardiovasc Surg. 2000 Apr;12(2):89-100. doi: 10.1053/ct.2000.5080. Semin Thorac Cardiovasc Surg. 2000. PMID: 10807431 Review.
The benign tumors include rhabdomyomas, fibromas, papillary fibroelastomas, hemangiomas, pericardial cysts, lipomas, hamartomas, teratomas, mesotheliomas, and paragangliomas or pheochromocytomas. The last 3 may also be malignant. The malignant tumors consist of vari …
The benign tumors include rhabdomyomas, fibromas, papillary fibroelastomas, hemangiomas, pericardial cysts, lipomas, hamartomas, teratomas, …
Malignant peripheral nerve sheath tumor: a study of 21 cases.
Chang SM, Ho WL. Chang SM, et al. Zhonghua Yi Xue Za Zhi (Taipei). 1994 Aug;54(2):122-30. Zhonghua Yi Xue Za Zhi (Taipei). 1994. PMID: 7954046
BACKGROUND: Malignant peripheral nerve sheath tumor (MPNST) is an aggressive tumor of neural origin. ...Aggressive surgical procedure with free resection margin is suggested. Malignant transformation should be highly suspected when …
BACKGROUND: Malignant peripheral nerve sheath tumor (MPNST) is an aggressive tumor of neural origi …
Pediatric malignant peripheral nerve sheath tumor: the Italian and German soft tissue sarcoma cooperative group.
Carli M, Ferrari A, Mattke A, Zanetti I, Casanova M, Bisogno G, Cecchetto G, Alaggio R, De Sio L, Koscielniak E, Sotti G, Treuner J. Carli M, et al. J Clin Oncol. 2005 Nov 20;23(33):8422-30. doi: 10.1200/JCO.2005.01.4886. J Clin Oncol. 2005. PMID: 16293873 Clinical Trial.
PURPOSE: To assess the value of chemotherapy and radiotherapy in children with malignant peripheral nerve sheath tumors (MPNSTs) and to identify risk factors associated with outcome. ...Postoperative radiotherapy may have a role in improving local cont …
PURPOSE: To assess the value of chemotherapy and radiotherapy in children with malignant peripheral nerve sheath …
Plexiform Neurofibroma Without Neurofibromatosis Type 1.
Wollina U, Schönlebe J. Wollina U, et al. Acta Dermatovenerol Croat. 2020 Dec;28(7):245-246. Acta Dermatovenerol Croat. 2020. PMID: 33835000
Dear Editor, Plexiform neurofibroma (PNF) is a particular subtype of benign nerve sheath tumors with a reticular growth pattern not respecting tissue borders and involving several nerve branches or fascicles. ...Malignant peripheral nerve …
Dear Editor, Plexiform neurofibroma (PNF) is a particular subtype of benign nerve sheath tumors with a reticular growth patter …
Dual mTORC1/2 inhibition induces anti-proliferative effect in NF1-associated plexiform neurofibroma and malignant peripheral nerve sheath tumor cells.
Varin J, Poulain L, Hivelin M, Nusbaum P, Hubas A, Laurendeau I, Lantieri L, Wolkenstein P, Vidaud M, Pasmant E, Chapuis N, Parfait B. Varin J, et al. Oncotarget. 2016 Jun 14;7(24):35753-35767. doi: 10.18632/oncotarget.7099. Oncotarget. 2016. PMID: 26840085 Free PMC article.
Approximately 30-50% of individuals with Neurofibromatosis type 1 develop benign peripheral nerve sheath tumors, called plexiform neurofibromas (PNFs). PNFs can undergo malignant transformation to highly metastatic malignant peripheral …
Approximately 30-50% of individuals with Neurofibromatosis type 1 develop benign peripheral nerve sheath tumors, called …
NTRK-Rearranged soft tissue neoplasms: A review of evolving diagnostic entities and algorithmic detection methods.
Surrey LF, Davis JL. Surrey LF, et al. Cancer Genet. 2022 Jan;260-261:6-13. doi: 10.1016/j.cancergen.2021.10.007. Epub 2021 Nov 3. Cancer Genet. 2022. PMID: 34794069
The pathology of NTRK rearranged tumors exists on a spectrum, with overlapping features of classic infantile fibrosarcoma, lipofibromatosis, and malignant peripheral nerve sheath tumor. In this tumor spectrum, clinical and pathologic p …
The pathology of NTRK rearranged tumors exists on a spectrum, with overlapping features of classic infantile fibrosarcoma, lipofibromatosis, …
TFG::MET-rearranged soft tissue tumor: A rare infantile neoplasm with a distinct low-grade triphasic morphology.
Michal M, Ud Din N, Švajdler M, Klubíčková N, Ptáková N, Hájková V, Michal M, Agaimy A. Michal M, et al. Genes Chromosomes Cancer. 2023 May;62(5):290-296. doi: 10.1002/gcc.23111. Epub 2022 Dec 13. Genes Chromosomes Cancer. 2023. PMID: 36464850
Both cases showed identical areas with a distinctive triphasic morphology resembling fibrous hamartoma of infancy (FHI), consisting of haphazardly arranged ovoid to spindled cells traversed by variably cellular and hyalinized fascicles admixed with (most likely non-neoplastic) ad …
Both cases showed identical areas with a distinctive triphasic morphology resembling fibrous hamartoma of infancy (FHI), consisting of hapha …
Carbon ion radiotherapy for unresectable retroperitoneal sarcomas.
Serizawa I, Kagei K, Kamada T, Imai R, Sugahara S, Okada T, Tsuji H, Ito H, Tsujii H. Serizawa I, et al. Int J Radiat Oncol Biol Phys. 2009 Nov 15;75(4):1105-10. doi: 10.1016/j.ijrobp.2008.12.019. Epub 2009 May 23. Int J Radiat Oncol Biol Phys. 2009. PMID: 19467578
PURPOSE: To evaluate the applicability of carbon ion radiotherapy (CIRT) for unresectable retroperitoneal sarcomas with regard to normal tissue morbidity and local tumor control. ...Of the patients, 16 had primary disease and 8 recurrent disease. Histologic diagnose …
PURPOSE: To evaluate the applicability of carbon ion radiotherapy (CIRT) for unresectable retroperitoneal sarcomas with regard to nor …
11 results