Zobrazeno 1 - 10
of 442
pro vyhledávání: '"Malignant peripheral nerve sheath tumour"'
Publikováno v:
Journal of Clinical and Scientific Research, Vol 12, Iss 2, Pp 81-87 (2023)
Background: Diverse lesions ranging from infective, inflammatory to neoplastic can occur in the hand. Almost all lesions that occur elsewhere in the body can affect the hand as well. Methods: This was a hospital-based retrospective study of 5 years d
Externí odkaz:
https://doaj.org/article/d49e17e5dc7c4a78a0f5c9d080ec5d29
Publikováno v:
Case Reports in Oncology, Vol 16, Iss 1, Pp 1-6 (2023)
Sporadically occurring malignant peripheral nerve sheath tumours (MPNSTs) can have a variety of genomic alterations including altered NF1, leading to activation of the RAS-RAF-MEK-ERK signalling pathway. Trametinib is an inhibitor of MEK1 and MEK2. H
Externí odkaz:
https://doaj.org/article/8fd79cf357fb47289da3df3126195a42
Autor:
Cecilie Ejerskov, Stense Farholt, Flemming Secher Kromann Nielsen, Ingunn Berg, Stine Bogetofte Thomasen, Aparna Udupi, Trude Ågesen, Sofie de Fine Licht, Mette Møller Handrup
Publikováno v:
Oncology and Therapy, Vol 11, Iss 1, Pp 97-110 (2022)
Abstract Introduction Plexiform neurofibromas (PN) are benign nerve sheath tumours that are a frequent and potentially debilitating complication in patients with neurofibromatosis type 1 (NF1). The objective of this study was to describe the natural
Externí odkaz:
https://doaj.org/article/25dcb177a4eb438fa7acbe2a23ac96a7
Autor:
Petković Sanja, Petković Stefan, Tadić-Latinović Ljiljana, Berendika Jelena, Tubić Biljana, Jungić Saša
Publikováno v:
Scripta Medica, Vol 53, Iss 2, Pp 165-169 (2022)
A malignant peripheral nerve sheath tumour (MPNST) is a highly aggressive sarcoma. This disease develops in a number of people with neurofibromatosis type 1 (NF1), which is a common genetic disease. The paper presents a patient with typical manifesta
Externí odkaz:
https://doaj.org/article/6e751559e2ea4c92a46d11b2e0981a92
Publikováno v:
African Journal of Urology, Vol 27, Iss 1, Pp 1-5 (2021)
Abstract Background Malignant peripheral nerve sheath tumour (MPNST) is a rare malignant soft tissue neoplasm of ectomesenchymal origin. They usually arise from a major or minor peripheral nerve branch or its sheath and also from somatic soft tissues
Externí odkaz:
https://doaj.org/article/e0a666c0a8d344bf8f37a1942accbbbb
Primary malignant peripheral nerve sheath tumour of the trachea: a case report and literature review
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 15, Iss 1, Pp 1-4 (2020)
Abstract Background Malignant peripheral nerve sheath tumours (MPNSTs) of the trachea are extremely uncommon neoplasms with unknown genetic and clinical profiles. Only individual cases have been reported in the literature to date. Case presentation H
Externí odkaz:
https://doaj.org/article/b9ab14bf49ed40f288d2f6276cac190f
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Central nervous system metastasis of an intradural malignant peripheral nerve sheath tumour in a dog
Publikováno v:
Open Veterinary Journal, Vol 9, Iss 1, Pp 49-53 (2019)
An 8-year-old French Bulldog was presented with a nonambulatory tetraparesis. Magnetic Resonance showed an intradurally located mass at the level of the right second cervical nerve root. The mass was surgically removed and the dog was ambulatory with
Externí odkaz:
https://doaj.org/article/8bfde2f34fff4ba1821a8a53c94248c9
Publikováno v:
Otolaryngology Case Reports, Vol 17, Iss , Pp 100212- (2020)
Malignant peripheral nerve sheath tumours are uncommon, aggressive tumours that are very rarely found in the head and neck. Whilst commonly associated with NF1 and radiotherapy, they can on occasion present sporadically. MPNSTs provide a challenge to
Externí odkaz:
https://doaj.org/article/06ce070c5c2743c989a453ee7b733147
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 14, Iss 8, Pp EC01-EC05 (2020)
Introduction: Mediastinal lesions are not frequently observed in routine clinical practice. A wide variety of disease process can occur within the mediastinum. Tissue from needle biopsies forms the major diagnostic material. There is need for deta
Externí odkaz:
https://doaj.org/article/760068844bf9442ab7aae084e1ee24a9