Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 11 de 11
Filter
2.
Neurosurgery ; 92(6): 1192-1198, 2023 06 01.
Article in English | MEDLINE | ID: mdl-36752634

ABSTRACT

BACKGROUND: Aneurysms of the posterior communicating segment of carotid artery (PcomA) have a high risk of rupture; when these nonruptured aneurysms are associated with oculomotor nerve palsy (ONP), the risk of rupture increases compared with asymptomatic nonruptured PcomA. OBJECTIVE: To retrospectively analyze the risk factors involved in ONP secondary to PcomA aneurysm and to study the factors involved in the recovery time of ONP once it is established. METHODS: This was a retrospective study of patients from 10 neurosurgery centers from October 2008 to December 2020. We analyzed age at diagnosis, presence of compressive neuropathy of the oculomotor nerve, presence of aneurysm rupture, largest aneurysm diameter, aneurysm projection, smoking, hypertension, diabetes, time between diagnosis and surgical treatment, as well as the outcome. RESULTS: Approximately 1 in 5 patients (119/511 23.3%) with a PcomA presented with ONP. We found that patients with aneurysms measuring greater than or equal to 7.5 mm were 1.6 times more likely to have ONP than those with aneurysms smaller than 7.5 mm. In our study, the prevalence of smoking in the PcomA + ONP group was 57.76%, and we also found that smokers were 2.51 times more likely to develop ONP. A total of 80.7% showed some degree of improvement, and 45.4% showed complete improvement with a median recovery time of 90 days. CONCLUSION: This study showed that 80.7% of patients with PcomA aneurysms undergoing surgical treatment with aneurysm clipping showed some degree of improvement of the ONP, with a median time to recovery between 90 and 120 days.


Subject(s)
Aneurysm, Ruptured , Endovascular Procedures , Intracranial Aneurysm , Oculomotor Nerve Diseases , Humans , Intracranial Aneurysm/complications , Intracranial Aneurysm/epidemiology , Intracranial Aneurysm/surgery , Retrospective Studies , Oculomotor Nerve Diseases/epidemiology , Oculomotor Nerve Diseases/surgery , Oculomotor Nerve Diseases/complications , Endovascular Procedures/adverse effects , Aneurysm, Ruptured/epidemiology , Aneurysm, Ruptured/surgery , Aneurysm, Ruptured/complications , Treatment Outcome
3.
Arq. bras. neurocir ; 40(3): 257-262, 15/09/2021.
Article in English | LILACS | ID: biblio-1362151

ABSTRACT

Pediatricmeningiomas are rare and account for only 2.2% of the central nervous system (CNS) tumors. In this age group, they aremore frequently located in atypical sites, such as, mainly, the ventricular system, with a frequency of 8.8 to 13.6%. Adding this to the fact that the angiomatous subtype constitutes only 2.1% of allmeningiomas, the rarity of the case reported here is corroborated. We report a 17-year-old female patient diagnosed with intraventricular angiomatous meningioma; she underwent surgical resection of the tumor in the body and frontal horn of the right lateral ventricle, and there were no neurological sequelae. With a follow-up of 26 months, there was no recurrence and the patient had clinical stability. Intraventricular tumors usually have slow growth and reach a considerable size until they cause symptoms and then are diagnosed. In addition, the deep location of the tumor and its proximity to eloquent areas make these tumors a neurosurgical challenge. The angiomatous subtype, due to the presence of hypervascularization (consisting of > 50% of vascular components), may, in some cases, hinder surgical resection as well as be erroneously diagnosed. However, surgical treatment aimed at total resection of the lesion remains the conduct of choice in the case reported here, especially in patients in the first two decades of life, in which the use of radiation is avoided. Specifically when it comes to the surgery, we chose a transcalosal approach that allows a good transoperative visualization of the lesion when located in the body and frontal horn of the lateral ventricle.


Subject(s)
Humans , Female , Adolescent , Lateral Ventricles/surgery , Meningeal Neoplasms/surgery , Meningioma/surgery , Treatment Outcome , Meningeal Neoplasms/diagnostic imaging , Meningioma/pathology , Meningioma/diagnostic imaging
4.
Neurosurg Focus Video ; 4(1): V14, 2021 Jan.
Article in English | MEDLINE | ID: mdl-36284612

ABSTRACT

Posterior fossa arteriovenous malformations (AVMs) can be a challenging disease, especially those large in size. AVMs can be treated with a combination of endovascular treatment and microsurgery. Here, the authors present the case of a 16-year-old female patient with progressive dizziness and episodic syncope. The workup of the patient showed a hemispheric cerebellar AVM, Spetzler-Martin grade IV. She underwent combined treatment (endovascular and microsurgery) with no complications and cure of the malformation. The video can be found here: https://youtu.be/rNw_Kyd76Mg.

5.
Oper Neurosurg (Hagerstown) ; 16(2): 48-49, 2019 Feb 01.
Article in English | MEDLINE | ID: mdl-29917106

ABSTRACT

The distal posterior inferior cerebellar artery (PICA) is a rare site of aneurysm formation. Only small case series and case reports regarding surgical treatment are found in the literature.The PICA is divided into 5 segments (anterior medullary, lateral medullary, tonsilomedullary, telovelotonsillary, and cortical), and the distal ones represent the most complex, due to anatomic variations. We present a case of a 69-yr-old female patient who has suffered from a sudden and intense occipital headache, associated with nausea and vomiting. CT scan showed intraventricular hemorrhage, and further investigation with MRI and MR Angiography revealed a small distal PICA aneurysm, at the superior part of the medial aspect of the left cerebellar tonsil. Digital angiography has demonstrated the aneurysm at the tonsilomedullary segment of the PICA. In this 3-dimensional video, the authors show the microsurgical clipping of a saccular distal PICA aneurysm in the close relation to a choroidal branch, performed by median suboccipital craniotomy. Step-by-step of the dissection, relevant surrounding anatomy and aneurysm clipping is demonstrated. The patient signed the Institutional Consent Form, which allows the use of his/her images and videos for any type of medical publications in conferences and/or scientific articles.

6.
World Neurosurg ; 2018 Dec 31.
Article in English | MEDLINE | ID: mdl-30605760

ABSTRACT

Basilar bifurcation is a challenging site for aneurysm clipping. Anatomical factors such as size and projection of the aneurysm, distance between the aneurysm neck and the dorsum sellae, and location of the basilar bifurcation contribute to surgical complexity. Endovascular treatment has been used more frequently than microsurgical clipping, especially for posterior circulation lesions. Thus, the upcoming generation of neurosurgeons will have increasingly less access to the microsurgical treatment of such lesions. We present the case of a 45-year-old female patient who presented sudden mental confusion characterized by disorientation in time, space, and person. Investigative acute cerebral magnetic resonance imaging revealed diffusion restriction in the left posterior cerebral and superior cerebellar arteries. The clinical and cardiologic investigations revealed no abnormalities, but computed tomographic angiography and digital arteriography revealed a low-riding basilar bifurcation aneurysm and a very small aneurysm in the right internal carotid artery. The wide neck precluded coil embolization, and the appropriate stent was not covered by our public health insurance. Considering the young age, surgical treatment was proposed. Microsurgical clipping was performed using the right pre-temporal approach. In this two-dimensional video, we show the steps to reach the low-riding basilar bifurcation aneurysm neck. The positioning, transzygomatic pterional craniotomy, intradural anterior clinoidectomy, and posterior cavernous sinus opening are shown, and the surrounding anatomy is illustrated.

8.
Arq Neuropsiquiatr ; 66(2A): 168-74, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18545776

ABSTRACT

OBJECTIVE: To describe the neurological outcome of newborns with seizures. METHOD: Cohort study with newborns prospectively followed. Perinatal characteristics and etiological screening were related to outcome in a regression model. RESULTS: During the study 3,659 newborns were admitted and 2.7% were diagnosed as having seizures. Hypoxic ischemic encephalopathy (51%) was the etiology more frequently associated to seizures and also to postneonatal epilepsy (53%). In the follow up 25 died during the acute neonatal illness and 9 during the first years of life, 19 were diagnosed as having post neonatal epilepsy, 35 had developmental delay and 11 an association among this two comorbidities. A significant association between abnormal postnatal EEG and neuroimaging to developmental delay (p=0.014, p=0.026) was observed. The group of newborns that had seizures presented an increased risk of developing epilepsy compared to newborns from the same cohort without seizures (19.3/100 vs. 1.8/100, p<0.001). CONCLUSION: In this study neonatal seizures predominated in term newborns with perinatal asphyxia an elevated perinatal mortality and post neonatal morbidity was observed. The follow up showed an increased risk for developing postnatal epilepsy and developmental delay.


Subject(s)
Brain Ischemia/complications , Developmental Disabilities/etiology , Epilepsy/etiology , Psychomotor Disorders/etiology , Seizures/complications , Brain Ischemia/congenital , Electroencephalography , Epidemiologic Methods , Female , Humans , Infant, Newborn , Male , Prognosis , Seizures/diagnosis
9.
Arq. neuropsiquiatr ; 66(2a): 168-174, jun. 2008. tab
Article in English | LILACS | ID: lil-484119

ABSTRACT

OBJECTIVE: To describe the neurological outcome of newborns with seizures. METHOD: Cohort study with newborns prospectively followed. Perinatal characteristics and etiological screening were related to outcome in a regression model. RESULTS: During the study 3659 newborns were admitted and 2.7 percent were diagnosed as having seizures. Hypoxic ischemic encephalopathy (51 percent) was the etiology more frequently associated to seizures and also to postneonatal epilepsy (53 percent). In the follow up 25 died during the acute neonatal illness and 9 during the first years of life, 19 were diagnosed as having post neonatal epilepsy, 35 had developmental delay and 11 an association among this two comorbidities. A significant association between abnormal postnatal EEG and neuroimaging to developmental delay (p=0.014, p=0.026) was observed. The group of newborns that had seizures presented an increased risk of developing epilepsy compared to newborns from the same cohort without seizures (19.3/100 vs. 1.8/100, p<0.001). CONCLUSION: In this study neonatal seizures predominated in term newborns with perinatal asphyxia an elevated perinatal mortality and post neonatal morbidity was observed.The follow up showed an increased risk for developing postnatal epilepsy and developmental delay.


OBJETIVO: Avaliar o prognóstico neurológico de neonatos com crises convulsivas. MÉTODO: Estudo prospectivo, realizado em coorte de neonatos provenientes de hospital terciário. As características clínicas perinatais e os resultados de exames complementares foram correlacionados com prognóstico através de modelo de regressão logística. RESULTADOS: Durante o estudo 3659 neonatos foram internados, sendo que 101 apresentaram crises convulsivas (2,7 por cento). A encefalopatia hipóxico-isquêmica foi a etiologia mais frequentemente associada às crises (51 por cento). O seguimento evidenciou 25 óbitos no período neonatal e 9 durante os primeiros anos de vida, 19 lactentes desenvolveram epilepsia, 35 atraso no desenvolvimento e 11 associação entre os dois desfechos. O modelo de regressão logística aplicado mostrou associação significativa entre EEG pós neonatal anormal e neuroimagem anormal com atraso no desenvolvimento (p=0,014, p=0,026). Os neonatos em estudo, quando comparados aos demais da mesma coorte, que não apresentaram crises convulsivas tiveram maior probabilidade de desenvolver epilepsia (19,3/100 vs. 1,8/100, p<0,001). CONCLUSÃO: Neste estudo em que ocorreu predomínio de crises neonatais em neonatos a termo com asfixia perinatal, foi observada alta mortalidade perinatal e morbidade. O seguimento neurológico evidenciou elevado risco de desenvolvimento de epilepsia e/ou atraso no desenvolvimento neuropsicomotor.


Subject(s)
Female , Humans , Infant, Newborn , Male , Brain Ischemia/complications , Developmental Disabilities/etiology , Epilepsy/etiology , Psychomotor Disorders/etiology , Seizures/complications , Brain Ischemia/congenital , Electroencephalography , Epidemiologic Methods , Prognosis , Seizures/diagnosis
10.
Acta méd. (Porto Alegre) ; 27: 319-329, 2006.
Article in Portuguese | LILACS | ID: lil-445193

ABSTRACT

A partir da descrição de um caso clínico de epilepsia do lobo temporal (elt), atendido no ambulatório de epilepsias graves do hospital são lucas da pucrs, os autores revisam os aspectos clínicos e fisiopatológicos dos traços de personalidade dita epilética. discutem ainda sua nosologia e relação dentro do espectro das alterações psiquiátricas em epilepsia.


Subject(s)
Humans , Behavior , Epilepsy, Temporal Lobe/physiopathology , Epilepsy, Temporal Lobe/psychology , Personality
11.
Rev. psiquiatr. Rio Gd. Sul ; 25(3): 453-465, dez. 2003. ilus
Article in Portuguese | LILACS-Express | LILACS | ID: lil-359624

ABSTRACT

OBJETIVO: descrever aspectos atualizados sobre as alterações e os distúrbios do sono no processo de envelhecimento normal e usual. MÉTODOS: procedeu-se a revisão da arquitetura do sono e ritmo circadiano de sono e vigília para estabelecer o padrão de normalidade e as alterações fisiológicas no processo de envelhecimento, descrevendo-se os distúrbios de sono mais prevalentes no idoso, sua avaliação diagnóstica e o manejo não-farmacológico. O texto foi elaborado a partir da consulta às publicações científicas indexadas no Medline, em outras de acesso on line e em livros textos das áreas de geriatria, psiquiátria geriátrica e medicina do sono. RESULTADOS E CONCLUSÃO: a maioria dos idosos tem queixas relacionadas ao sono decorrentes de mudanças fisiológicas específicas do processo de envelhecimento ou de doenças que podem causar distúrbios secundários de sono. A linha divisória entre a normalidade e o distúrbio pode ser estabelecida por meio de criteriosa avaliação diagnóstica, a qual necessariamente precede e orienta a conduta terapêutica. A maioria dos distúrbios de sono são clinicamente importantes e tratáveis com medidas não-farmacológicas, que incluem a orientação sobre rotinas e rituais de sono, atividades de vida diária e condições ambientais.

SELECTION OF CITATIONS
SEARCH DETAIL
...