Patient with neurofibromatosis type 1 and supratentorial tumor
Keywords:
neurofibromatosis 1, supratentorial neoplasms/diagnosisAbstract
The case of a 24-year-old male patient who had a history of neurofibromatosis type 1 and was admitted with headache, vomiting and dysarthria is reported. It was determined the existence of a supratentorial tumor, with a diagnosis of glial tumor of the type diffuse fibrillary astrocytoma grade IV. The report of various tumors associated with Von Recklinghausen's disease, and the imaging and morphological characteristics described, motivated a review the classification of the World Health Organization for tumors of the central nervous system and the classification of St Anne-Mayo for hemispheric tumors, allowing its proper location and its differentiation from other intracranial neoplasms that have been described in patients with the disease. The survival of the patient, for 20 months to date, coincides with the location of the tumor as a slower growing tumor that has undergone an anaplastic transformation, which has a relatively better prognosis.Downloads
Downloads
How to Cite
Issue
Section
License
Authors who have publications with this journal agree to the following terms:
- Authors will retain their copyright and assign to the journal the right of first publication of their work, which will simultaneously be subject to a Creative Commons License / Attribution-Noncommercial 4.0 International (CC BY-NC 4.0) that allows third parties to share the work as long as its author and first publication in this journal are indicated.
- Authors may adopt other non-exclusive license agreements for distribution of the published version of the work (e.g., depositing it in an institutional repository or publishing it in a monographic volume) as long as the initial publication in this journal is indicated.
- Authors are allowed and encouraged to disseminate their work through the Internet (e.g., in institutional telematic archives or on their web page) before and during the submission process, which can produce interesting exchanges and increase citations of the published work. (See The effect of open access).