Zobrazeno 1 - 10
of 4 492
pro vyhledávání: '"peripheral nerve sheath tumor"'
Autor:
Marie-Lena Schmalhofer, Said Farschtschi, Lan Kluwe, Victor Felix Mautner, Gerhard Adam, Lennart Well, Inka Ristow
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Patients with neurofibromatosis type 1 (NF1) can develop plexiform neurofibromas (PN). Large tumor burden is a predictor for the development of malignant peripheral nerve sheath tumors. Whole-body magnetic resonance imaging (WB-MR
Externí odkaz:
https://doaj.org/article/8d7edd8b3f144e49abd5b06f094fd6de
Autor:
Jeffrey Rosenthal, MD, Chukwuemeka Okoro, MD, Naomi Walker, MD, Scott Nelson, MD, Nicholas Bernthal, MD, Varand Ghazikhanian, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 6080-6084 (2024)
Peripheral nerve sheath tumors are a heterogenous group of predominantly benign tumors of neurogenic origin that arise outside of the central nervous system and include schwannomas and neurofibromas. These tumors often occur sporadically, however mul
Externí odkaz:
https://doaj.org/article/cb85fe930ed64c72b7461e5ea22fd192
Autor:
A. Yu. Orlov, A. S. Nazarov, A. A. Dolgushin, D. A. Murzaeva, Yu. V. Belyakov, E. A. Oleynik, A. V. Kudziev, Yu. M. Zabrodskaya
Publikováno v:
Сибирский онкологический журнал, Vol 23, Iss 3, Pp 32-43 (2024)
Peripheral nerve sheaths tumors (PNST) account for about 8 % of all nervous system cancers. The relapse rate ranges from 17.3 to 26.4 %, showing an upward trend. The causes and provoking factors for the development of relapses of PNST have not been f
Externí odkaz:
https://doaj.org/article/d6492cf4d31c4e378598af024cdd6b95
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
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
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