دورية أكاديمية

Gliosarcoma in a young patient with neurofibromatosis type 1. Case report

التفاصيل البيبلوغرافية
العنوان: Gliosarcoma in a young patient with neurofibromatosis type 1. Case report
المؤلفون: Luisa Fernanda Zúñiga-Cerón, Jhan Sebastián Saavedra-Torres, Tomás Omar Zamora-Bastidas, María Virginia Pinzón-Fernández
المصدر: Case Reports, Vol 4, Iss 2, Pp 91-98 (2018)
بيانات النشر: Universidad Nacional de Colombia
سنة النشر: 2018
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Neurofibromatosis 1, Gliosarcoma, Glioblastoma, Neurofibroma, Medicine (General), R5-920
الوصف: Introduction: Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder that has variable phenotypic expressivity, with manifestations ranging from cutaneous lesions to functional compromise. It manifests clinically during childhood and adolescence. The NF-1 gene encodes a protein, neurofibromin gene, which acts as a tumor suppressor under normal conditions by regulating another protein that stimulates cell growth and proliferation. In case of alteration, different tumor processes may occur, such as the one seen in a small number of cases. Case presentation: 20-year-old male patient with NF1, who presented café-au-lait spots and developed a glioblastoma, which happens infrequently. Discussion: Immunohistochemistry methods that contribute greatly to prognosis are included to achieve the confirmed diagnosis since the median overall survival of glioblastoma patients is higher in patients with NF1 than in those without said pathological entity. Conclusion: The early diagnosis of the lesions favors a timely management of NF1. These patients require a comprehensive and interdisciplinary management to achieve full rehabilitation.
نوع الوثيقة: article in journal/newspaper
اللغة: English
Spanish; Castilian
تدمد: 2462-8522
العلاقة: https://revistas.unal.edu.co/index.php/care/article/view/68234Test; https://doaj.org/toc/2462-8522Test; https://doaj.org/article/bfb2ea8c96154dff8f23861d8dbd015fTest
DOI: 10.15446/cr.v4n2.68234
الإتاحة: https://doi.org/10.15446/cr.v4n2.68234Test
https://doaj.org/article/bfb2ea8c96154dff8f23861d8dbd015fTest
رقم الانضمام: edsbas.76AB2E22
قاعدة البيانات: BASE
الوصف
تدمد:24628522
DOI:10.15446/cr.v4n2.68234