Cervicomedullary Junction Ependymoma Associated with Neurofibromatosis Type II: Case Report and Literature Review
Autor: | Helder Tedeschi, Otávio Turolo da Silva, Enrico Ghizoni, Carlos Eduardo Vasconcelos Miranda, Andrei Fernandes Joaquim, Luciano de Souza Queiroz |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
Ependymoma
medicine.medical_specialty ependymoma business.industry lcsh:R lcsh:Surgery lcsh:Medicine lcsh:RD1-811 medicine.disease Cervicomedullary Junction Resection Surgery neurofibromatosis type ii surgery Rare case otorhinolaryngologic diseases Medicine Neurology (clinical) Inherited disease Neurofibromatosis Presentation (obstetrics) business Surgical treatment |
Zdroj: | Brazilian Neurosurgery, Vol 36, Iss 01, Pp 54-57 (2017) |
ISSN: | 2359-5922 0103-5355 |
Popis: | Neurofibromatosis type II (NF2) is a rare autosomal dominant inherited disease caused by a mutation in chromosome 22q12 and associated with multiple central nervous system tumors. In this paper, we describe a rare case of cervicomedullary junction ependymoma associated with NF2 in a 25-year-old man who underwent surgical treatment with total resection and had a good clinical outcome. We discussed the nuances of the surgical resection and the literature concerning this rare form of presentation of NF2. |
Databáze: | OpenAIRE |
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