Produção Nacional
Revisado por pares
Magnetic resonance findings of neurofibromatosis type 2: a case report
2009; BioMed Central; Volume: 2; Issue: 1 Linguagem: Inglês
10.4076/1757-1626-2-6720
ISSN1757-1626
AutoresGabriela Spilberg, Edson Marchiori, Emerson L. Gasparetto, Rafael Ferracini Cabral, Tatiana Chinem Takayassu, Raquel Batista, Isabela Garcia Vieira,
Tópico(s)Vascular Malformations Diagnosis and Treatment
ResumoNeurofibromatosis type 2 is an inherited autosomal dominant syndrome, characterized by multiple neoplasms of the central and peripheral nervous system associated with ocular abnormalities. The most common tumor associated with the disease is the vestibulocochlear schwannoma (VIII cranial nerve), and as many as 10% of patients with this tumor have neurofibromatosis type 2. In this report we aim to present a 34-year-old male who was seen for bilateral hearing loss. During his workup, which included cranial computer tomography, he was found to have multiple intracranial masses. Cranial and whole spine magnetic resonance imaging showed bilateral vestibulocochlear schwannoma, multiple meningiomas, and one intramedullary tumor. Based on clinical and imaging findings the diagnostic of neurofibromatosis type 2 was made.
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