Tumores de Sistema Nervioso asociados con la Neurofibromatosis tipo 1 y 2
محفوظ في:
| المؤلفون: | , |
|---|---|
| التنسيق: | artículo original |
| الحالة: | Versión publicada |
| تاريخ النشر: | 2018 |
| الوصف: | Neurofibromatosis, today understood as a concept including two different entities (type 1 and type 2), is a genetic disease part of the neurocutaneous syndromes, initially described in 1849 that nowadays remains widely studied due to its complex physiopathology. is mechanism has been partially attributed due to mutations in tumoral suppressor genes, allowing uncontrolled cellular proliferation, producing different benign and cancerous neoplasia that characterized the disease. e clinical picture is complemented by affection of other body systems. Among the tumors that compose this entity are neurofibromas, plexiform neurofibromas, nerve sheath malign tumors, gliomas, schwannomas, meningiomas and ependimomas. e approach to these tumors, consisting principally in image study follow ups, surgery and chemotherapy, is currently not unified by international guidelines by the respective worldwide entities. |
| البلد: | Portal de Revistas UCR |
| المؤسسة: | Universidad de Costa Rica |
| Repositorio: | Portal de Revistas UCR |
| اللغة: | Español |
| OAI Identifier: | oai:portal.ucr.ac.cr:article/36061 |
| الوصول للمادة أونلاين: | https://revistas.ucr.ac.cr/index.php/clinica/article/view/36061 |