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1.
Epileptic Disord ; 25(4): 480-491, 2023 08.
Artigo em Inglês | MEDLINE | ID: mdl-37309048

RESUMO

OBJECTIVE: Eating-induced seizures (EIS) are a rare form of reflex seizures. The objective of this study was to report a series of cases of EIS involving patients admitted to our epilepsy unit, and to analyze the clinical characteristics, etiology, and treatment response of this type of infrequent seizure. METHODS: We performed a single-center retrospective analysis of all consecutive patients diagnosed with epilepsy with eating-induced seizures between 2008 and 2020. RESULTS: We included eight patients (six women) with mean age 54.75 years (range: 40-79), and mean age at epilepsy onset 30.75 years (range: 9-58 years). EIS were triggered during a meal in 5/8 (at dinner 1/8, at breakfast in 1/8, and without time preference in 3/8), by a certain flavor in 1/8, by eating different textures or drinking soft drinks in 1/8, and by slicing food in 1/8. All patients suffered nonreflex seizures and 3/8 other types of reflex seizures. In 6/8 of patients, EIS originated in the right hemisphere. In 5/8, the EIS progressed to impaired awareness with oromandibular automatisms. In 6/8, the epilepsy was drug-resistant. Temporopolar encephalocele was the most frequent etiology, in 4/8. Three of the eight underwent surgical treatment, with Engel IA 1 year in 3/3. Three of the eight were treated with vagal stimulation therapy, with McHugh A 1 year in 2/3. SIGNIFICANCE: In our series, eating-induced seizures were observed in patients with focal epilepsy. It was frequently drug-resistant and started predominantly in the right hemisphere, due to temporal pole involvement in half of the patients.


Assuntos
Epilepsia do Lobo Temporal , Epilepsia , Humanos , Feminino , Pessoa de Meia-Idade , Criança , Adolescente , Adulto Jovem , Adulto , Estudos Retrospectivos , Eletroencefalografia , Convulsões/diagnóstico , Lobo Temporal/cirurgia , Epilepsia/complicações , Epilepsia do Lobo Temporal/etiologia , Epilepsia do Lobo Temporal/cirurgia
2.
Neurocirugía (Soc. Luso-Esp. Neurocir.) ; 30(2): 81-86, mar.-abr. 2019. ilus, tab
Artigo em Inglês | IBECS | ID: ibc-182006

RESUMO

Anterior cervical discectomy has a low non-mechanical complication rate. In our literature review, we found 7 cases of delayed surgical site infection. We report a case of cervical prevertebral abscess due to Propionibacterium acnes 2 years after discectomy and arthroplasty, with a beta-2-transferrin false positive test as a complementary highlighted finding. We discuss the diagnosis and etiology of this rare delayed infectious complication


La discectomía cervical anterior tiene una baja tasa de complicaciones no mecánicas. En la revisión de la literatura, encontramos 7 casos de infección diferida del sitio quirúrgico. Presentamos un caso de absceso cervical prevertebral secundario a Propionibacterium acnes 2 años después de la cirugía, asociado a un falso positivo del test de beta-2-transferrina como hallazgo complementario a destacar, y discutimos el diagnóstico y la etiología de esta rara complicación infecciosa diferida


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Infecção da Ferida Cirúrgica/etiologia , Plexo Cervical/cirurgia , Artroplastia/métodos , Tempo para o Tratamento , Abscesso/complicações , Infecção da Ferida Cirúrgica/complicações , Complicações Pós-Operatórias/prevenção & controle , Fatores de Tempo , Cicatrização
3.
Neurocirugia (Astur : Engl Ed) ; 30(2): 81-86, 2019.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-29627290

RESUMO

Anterior cervical discectomy has a low non-mechanical complication rate. In our literature review, we found 7 cases of delayed surgical site infection. We report a case of cervical prevertebral abscess due to Propionibacterium acnes 2 years after discectomy and arthroplasty, with a beta-2-transferrin false positive test as a complementary highlighted finding. We discuss the diagnosis and etiology of this rare delayed infectious complication.


Assuntos
Abscesso/diagnóstico por imagem , Artroplastia , Vértebras Cervicais/cirurgia , Discotomia , Infecções por Bactérias Gram-Positivas/diagnóstico por imagem , Deslocamento do Disco Intervertebral/cirurgia , Propionibacterium acnes , Fusão Vertebral , Infecção da Ferida Cirúrgica/diagnóstico por imagem , Humanos , Masculino , Pessoa de Meia-Idade , Fatores de Tempo
4.
World Neurosurg ; 108: 996.e17-996.e25, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-28939541

RESUMO

BACKGROUND: Composite ganglioma and pleomorphic xanthoastrocytoma with anaplastic features in both components is an extremely rare glioneuronal tumor. Five cases of anaplastic progression in the glioma component have been reported. These tumors generally affect young patients who have brain tumor-related epilepsy, which are usually located in the temporal lobe or in the cerebellum and may have associated leptomeningeal spreading. Its current optimal treatment consists of maximal safe surgical resection and adjuvant chemoradiotherapy. Overall survival at 5 years is 33% in anaplastic pleomorphic xanthoastrocytoma and 53% in anaplastic ganglioglioma. CASE DESCRIPTION: We describe a progression from ganglioglioma to this composite anaplastic entity after 32 months of follow-up, with apparently nontumoral parenchyma separating the 2 components. Polymerase chain reaction showed a wild-type BRAF gene. Seven months after concomitant chemoradiotherapy, radiologic progression led to a second line of chemotherapy, and a third line of chemotherapy was initiated after a subsequent progression at 11 months. CONCLUSIONS: This case may add some evidence in favor of the glioneuronal maldevelopment hypothesis to explain the oncogenesis of these neuroepithelial tumors.


Assuntos
Astrocitoma/diagnóstico por imagem , Neoplasias Encefálicas/diagnóstico por imagem , Ganglioglioma/diagnóstico por imagem , Neoplasias Complexas Mistas/diagnóstico por imagem , Adulto , Astrocitoma/complicações , Astrocitoma/patologia , Astrocitoma/terapia , Neoplasias Encefálicas/complicações , Neoplasias Encefálicas/terapia , Progressão da Doença , Epilepsia do Lobo Temporal/etiologia , Feminino , Ganglioglioma/complicações , Ganglioglioma/patologia , Ganglioglioma/terapia , Humanos , Imageamento por Ressonância Magnética , Neoplasias Complexas Mistas/complicações , Neoplasias Complexas Mistas/terapia
5.
Neurosurgery ; 81(4): 585-594, 2017 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-28327942

RESUMO

BACKGROUND: Intraoperative identification and preservation of the corticospinal tract is often necessary for glioma resection. OBJECTIVE: To make a proposal for intraoperative management with the high-frequency monopolar stimulation technique for monitoring the corticospinal tract. METHODS: Ninety-two patients operated on with the assistance of the high-frequency monopolar stimulation. Clinical and neurophysiological data have been related with the motor status at 3 months to establish prognostic factors of motor deterioration. RESULTS: Twenty-one patients (22.8%) presented intraoperative alterations in motor-evoked potentials (MEPs). Twelve (13%) presented an increment in the MEP threshold ≥5 mA (no deficit at 3 months). Two (2.2%) presented an MEP amplitude reduction >50% (100% deficit at 3 months). Seven (7.6%) had an intraoperative MEP loss (80% deficit at 3 months). Subcortical stimulation was positive in 75 patients (81.5%). Eighty-five patients were available for the analysis at 3 months. Fourteen presented new deficits (16.5%). Among them, 5 presented a deficit in nonmonitored muscles (5.9%) and 1 presented a new deficit not detected intraoperatively. The combination of patients with preoperative motor deficits, MEP deterioration, or loss and intensity of subcortical stimulation ≤3 mA showed the highest sensitivity and specificity in the prediction of new deficits. CONCLUSIONS: Persistent MEP loss or deterioration is associated with a high probability of new deficits. It seems recommendable to stop the subcortical resection before obtaining a subcortical MEP threshold at 3 mA especially in patients with preoperative motor deficits. A careful selection of muscles for the registration of MEPs is mandatory to avoid deficits in nonmonitored muscles.


Assuntos
Mapeamento Encefálico/normas , Neoplasias Encefálicas/cirurgia , Estimulação Encefálica Profunda/normas , Glioma/cirurgia , Monitorização Neurofisiológica Intraoperatória/normas , Tratos Piramidais/cirurgia , Adulto , Idoso , Mapeamento Encefálico/métodos , Neoplasias Encefálicas/fisiopatologia , Estimulação Encefálica Profunda/métodos , Potencial Evocado Motor/fisiologia , Feminino , Glioma/fisiopatologia , Humanos , Monitorização Neurofisiológica Intraoperatória/métodos , Masculino , Pessoa de Meia-Idade , Tratos Piramidais/fisiologia
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