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1.
Arq. bras. neurocir ; 38(1): 20-24, 15/03/2019.
Article in English | LILACS | ID: biblio-1362622

ABSTRACT

Introduction Cerebellopontine angle (CPA) tumors represent an important cause of persistent and refractory trigeminal neuralgia (TN). It is believed that between 1 and 9.9% of the cases of patients presenting with TN painful manifestation are caused by space-occupying lesions. Objective The objective of the present study is to describe the clinical and surgical experience of the operative management of patients presenting with secondary type TN associated with CPA tumors. Method An observational investigation was conducted with data collection from patients with secondary type TN associated with CPA tumors who were treated with surgical resection of the space-occupying lesion and decompression of the trigeminal nerve from January 2013 to November 2016 in 2 different centers in the western region of the state of São Paulo, Brazil. Results We operated on 11 consecutive cases in which TN was associated with CPA during the period of analysis. Seven (63.6%) patients were female, and 4 (36.4%) were male. Seven (63.6%) patients presented with right-side symptoms, and 4 (36.4%) presented with left-side symptoms. After 2 years of follow-up, we observed that 8 (72.7%) patients showed a complete improvement of the symptoms, with an excellent outcome, and that 3 (27.3%) patients showed an incomplete improvement, with a good outcome. No patient reported partial improvement or poor outcome after the follow-up. There was no operative mortality. Conclusion Cerebellopontine angle tumors represent an important cause of TNandmust be included in the differential diagnosis of patients presenting with refractory and persistent symptoms. Surgical treatment with total resection of the expansive lesion and effective decompression of the trigeminal nerve are essential steps to control the symptoms.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Postoperative Complications , Trigeminal Neuralgia/surgery , Trigeminal Neuralgia/diagnostic imaging , Neuroma, Acoustic/complications , Medical Records , Statistics, Nonparametric , Decompression, Surgical/methods , Observational Study
2.
Arq. bras. neurocir ; 35(3): 248-252, 20/09/2016.
Article in English | LILACS | ID: biblio-910738

ABSTRACT

Dural arteriovenous fistulas (DAVFs) are pathologic dural shunts characterized by meningeal arterial supply, absence of nidus and drainage to dural venous sinuses or cortical veins. They are usually acquired lesions associated with specific disease and inflammatory processes, including craniotomy. We report a case of postoperative DAVF in a 59 year-old male presenting with a ruptured distal right anterior cerebral artery aneurysm. After an uneventful microsurgery for clipping, meningitis occurred on the ninth day, and was successfully treated. The one-year control angiogram showed a left occipital DAVF. The relevant literature on the occurrence of DAVFs is also presented.


Fístulas arteriovenosas durais (FAVDs) são comunicações patológicas caracterizadas por suprimento arterial meníngeo, ausência de nidus e drenagem para seios venosos durais ou veias corticais. As fístulas são geralmente adquiridas, secundárias a processos inflamatórios e doenças específicas, podendo ocorrer após craniotomia. Relatamos um caso de FAVD ocorrido em um homem de 59 anos de idade com aneurisma intracraniano roto em artéria cerebral anterior direita distal, submetido a microcirurgia e clipagem, e evoluindo com meningite pós-operatória. O paciente apresentou boa evolução, mas na angiografia de controle um ano após a cirurgia foi identificada FAVD em seio transverso-sigmoide esquerdo. Uma revisão da literatura focada na etiologia também é apresentada.


Subject(s)
Humans , Male , Middle Aged , Arteriovenous Fistula , Aneurysm, Ruptured
3.
J. bras. neurocir ; 21(3): 179-181, 2010.
Article in English | LILACS | ID: lil-579603

ABSTRACT

A doença de Behcet é caracterizada por uma condição inflamatóriacronica, multissistemica e recorrente, que podeapresentar manifestações vasculares e neurológicas duranteseu curso. Raramente encontramos associação desta afecçãocom aneurismas cerebrais e quando presente, o predomínio éna circulação anterior. Descrevemos um caso raro de doençade Behcet associado a aneurisma roto da artéria vertebralsubmetido a tratamento endovascular.


Subject(s)
Aneurysm , Behcet Syndrome
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