Zobrazeno 1 - 10
of 3 867
pro vyhledávání: '"malignant peripheral nerve sheath tumor"'
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 10, Iss 3, Pp 219-226 (2024)
Background: Malignant peripheral nerve sheath tumors (MPNSTs) are uncommon tumors typically originating from somatic soft tissues or peripheral nerves. Instances of primary MPNSTs on the scalp are exceedingly rare. Our objective is to present a uniqu
Externí odkaz:
https://doaj.org/article/eba65c73f30d4ec99cb0cf97f3533581
Publikováno v:
Asia Oceania Journal of Nuclear Medicine and Biology, Vol 12, Iss 2, Pp 174-178 (2024)
Malignant peripheral nerve sheath tumors (MPNST) are rare, aggressive soft tissue sarcomas that arise from peripheral nerves and often present a diagnostic and therapeutic challenge. They can occur sporadically or in association with neurofibromatosi
Externí odkaz:
https://doaj.org/article/48313c22a31b4c7aa4f87a7c63caed3f
Autor:
Anastasia Drakos, BHSc, Augusto Goncalves Filho, MD, MPH, John Woulfe, MD, PhD, FRCPC, Paulo Puac Polanco, MD, Eduardo Portela de Oliveira, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 7, Pp 2654-2662 (2024)
Stereotactic radiosurgery (SRS) is an effective treatment for vestibular schwannomas, offering high rates of tumor control and low neurological risks. Long-term complications of SRS are not fully understood, with several cases of malignant transforma
Externí odkaz:
https://doaj.org/article/d57fc79bd24846aeb19fb924c0bcf660
Autor:
Adisalem M. Teferi, Sangam Sangam, Azana Newman, Osman Alvarado, Irvianny Madera, Julian Paniagua
Publikováno v:
European Journal of Case Reports in Internal Medicine (2024)
Peripheral malignant nerve sheath tumours (MPNST) are rare and aggressive soft tissue sarcomas often associated with neurofibromatosis type I (NF-1). We describe a case of a 26-year-old female with NF-1, initially misdiagnosed as sciatica, who was la
Externí odkaz:
https://doaj.org/article/c0d5a505985f46178015b65c68b51efd
Publikováno v:
Journal of Immunotherapy and Precision Oncology, Vol 7, Iss 2, Pp 122-125 (2024)
ABSTRACT: Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder that primarily causes the growth of tumors alongnerves. Additionally, the germline mutations involved in NF1 predispose patients to develop further malignancies. The m
Externí odkaz:
https://doaj.org/article/9383a44b830f4e848e207ffe267ac387
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Primary intraosseous malignant peripheral nerve sheath tumors (MPNSTs) are rare yet highly aggressive neoplasms originating from peripheral nerves. Typically manifesting as soft tissue masses accompanied by pain or functional impairment, these tumors
Externí odkaz:
https://doaj.org/article/2b6647a3720d4471895d249f173edf5f
Autor:
E. V. Krishnakumar, Sandhra Satish, Joy Augustine, K. K. Ajaykumar, C. Davis Paul, N. A. Arun, P. Unnikrishnan
Publikováno v:
Journal of Advanced Lung Health, Vol 4, Iss 3, Pp 186-188 (2024)
A 28-year-old female, a known case of neurofibromatosis 1, presented to the respiratory medicine department with complaints of breathlessness and cough for 2 weeks’ duration. Clinical examination revealed right-sided moderate pleural effusion. Comp
Externí odkaz:
https://doaj.org/article/003b4126f9674ea0aec1356486cf7002
Autor:
Julia A. Nikrad, Robert T. Galvin, Mackenzie M. Sheehy, Ethan L. Novacek, Kari L. Jacobsen, Stanislas M.A.S. Corbière, Pauline J. Beckmann, Tyler A. Jubenville, Masato Yamamoto, David A. Largaespada
Publikováno v:
Molecular Therapy: Oncology, Vol 32, Iss 2, Pp 200783- (2024)
Oncolytic adenoviruses (Ads) stand out as a promising strategy for the targeted infection and lysis of tumor cells, with well-established clinical utility across various malignancies. This study delves into the therapeutic potential of oncolytic Ads
Externí odkaz:
https://doaj.org/article/7082c4ce0bb244fca6dec11d2d2154ac
Autor:
Yeaseul Kim, Uksha Saini, Doyeon Kim, Ilse Hernandez-Aguirre, Jack Hedberg, Alexia Martin, Xiaokui Mo, Timothy P. Cripe, James Markert, Kevin A. Cassady, Ravi Dhital
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionMalignant peripheral nerve sheath tumors (MPNSTs) are aggressive sarcomas with unacceptably low cure rates occurring often in patients with neurofibromatosis 1 defects. To investigate oncolytic Herpes Simplex Virus (oHSV) as an immunother
Externí odkaz:
https://doaj.org/article/5f74ff6d85764633914ea8330bf8e162
Autor:
Hyun Woo, Hyeyoung Kwon, Jin Hwan Kim, Song Soo Kim, Hyung Kyu Park, Younju Rhee, Jae-Hyeong Park
Publikováno v:
Journal of the Korean Society of Radiology, Vol 84, Iss 6, Pp 1384-1390 (2023)
Primary masses rarely originate from the heart and great vessels, and a malignant peripheral nerve sheath tumor (MPNST) is extremely rare. A 76-year-old male with pleural effusion underwent contrast- enhanced computed tomography, which revealed a h
Externí odkaz:
https://doaj.org/article/12706437c7564a0384468d75605dee96