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1.
No Shinkei Geka ; 48(7): 607-613, 2020 Jul.
Artigo em Japonês | MEDLINE | ID: mdl-32694230

RESUMO

Herein, we report a rare case of penetrating transorbital cavernous sinus injury caused by a bamboo stick, treated by craniotomy in a hybrid operating room. A 63-year-old gardener presented at our hospital with right upper orbital injury after falling on a bamboo basket. Neurological examination revealed right II, III, IV, and VI cranial nerve palsies. CT and MRI revealed a right transorbital penetrating injury by a small sharp wooden foreign body, extending from the orbit to the cavernous sinus via the superior orbital fissure. Preoperative digital subtraction angiography revealed partial occlusion of the right cavernous sinus by the foreign body and no internal carotid artery(ICA)injury. There was a nine-day waiting period after the injury because the patient was on dual antiplatelet therapy for ischemic heart disease. Subsequently, the bamboo stick was completely removed through the right fronto-temporo-orbito-zygomatic approach in a hybrid operating room. To treat the potential massive hemorrhage, a five-French balloon catheter was inserted in the right ICA at its origin via the right transfemoral approach before the craniotomy. The bamboo stick was completely removed with minor hemorrhage in the cavernous sinus; this was controlled using hemostatic materials. The postoperative course was uneventful. The patient was discharged with blindness and total ophthalmoplegia in the right eye but he was able to return to his prior job. This is the first report of such a treatment of a transorbital penetrating injury in a hybrid operating room.


Assuntos
Seio Cavernoso/cirurgia , Ferimentos Penetrantes/cirurgia , Craniotomia , Humanos , Masculino , Pessoa de Meia-Idade , Salas Cirúrgicas , Órbita/cirurgia
2.
No Shinkei Geka ; 46(5): 405-411, 2018 May.
Artigo em Japonês | MEDLINE | ID: mdl-29794317

RESUMO

A 16-year-old boy collided with a passenger car while riding a motorcycle. He was thrown to a distance and experienced a head injury on impact. When brought to our medical facility, he was alert, had no neurological abnormalities, and did not complain of headache. A head computed tomography(CT)scan indicated a left cranial fracture and an acute epidural hematoma(15mm thick)directly under the fracture. Follow-up head CT performed 3 hours after the injury indicated no change in the size of the hematoma. The head CT performed on the following day indicated that most of the hematoma had disappeared. As the patient had neither headache nor neurological symptoms, he was placed under observation. However, a head CT performed 7 days after the injury indicated the formation of an epidural hematoma approximately the same size as the initial hematoma and located at the same site. We performed craniotomy to evacuate the hematoma, identify the source of the bleeding, and restore hemostasis. Although cases in which an acute epidural hematoma rapidly and spontaneously resolves have been reported, these are extremely rare. Recurrence of an epidural hematoma despite normal blood coagulation function after its initial rapid resolution has not been reported yet. We report on this rare case of acute epidural hematoma with reference to relevant literatures.


Assuntos
Traumatismos Craniocerebrais , Hematoma Epidural Craniano , Adolescente , Traumatismos Craniocerebrais/complicações , Craniotomia , Hematoma Epidural Craniano/etiologia , Humanos , Masculino , Recidiva , Remissão Espontânea , Tomografia Computadorizada por Raios X
3.
World Neurosurg ; 83(5): 842-51, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25683130

RESUMO

OBJECTIVE: Aneurysms of the posterior cerebral artery (PCA) are rare, and therefore the individual and institutional experience of their microsurgical management is usually limited. In the present article, we describe our experience with the subtemporal approach to aneurysms arising from the PCA. METHODS: We reviewed 34 patients diagnosed with 37 PCA aneurysms, all microsurgically managed using the subtemporal approach between 1980 and 2012 at 2 Finnish neurosurgical centers (Helsinki and Kuopio). The following procedures were applied using the subtemporal approach: neck clipping (n = 24); proximal occlusion (n = 7); trapping (n = 2); wrapping (n = 1); aneurysmoraphy (n = 1); bypass bridging/trapping (n = 1); and a complex excimer laser-assisted nonocclusive anastomosis procedure (n = 1). RESULTS: Of these 34 patients, 16 presented with acute subarachnoid hemorrhage as a result of PCA aneurysm rupture, and 11 of the 16 had good outcome (modified Rankin scale 0-2) at 3 months The remaining 18 patients were treated microsurgically for incidentally diagnosed unruptured aneurysms, and 14 of the 18 had a good outcome. The most common serious complication in this series was an ipsilateral PCA infarction (12/34; 35%), mostly after proximal occlusion (n = 7) and/or trapping (n = 2). CONCLUSIONS: The subtemporal approach is a suitable approach to aneurysms of the segments P1, P1-P2 junction, and P2, as well as the anterior P3 segment of the PCA. Using the subtemporal approach, the cerebrospinal fluid is released before retraction is necessary to prevent temporal lobe injury. The subtemporal approach can provide enough space for revascularization procedures. The most encountered complications were not related to the subtemporal approach but to the specific nature of PCA aneurysms.


Assuntos
Fístula Arteriovenosa/cirurgia , Aneurisma Intracraniano/cirurgia , Procedimentos Neurocirúrgicos/métodos , Artéria Cerebral Posterior/cirurgia , Lobo Temporal/cirurgia , Adolescente , Adulto , Idoso , Aneurisma Roto/cirurgia , Fístula Arteriovenosa/patologia , Criança , Craniotomia/métodos , Bases de Dados Factuais , Feminino , Seguimentos , Humanos , Aneurisma Intracraniano/patologia , Masculino , Pessoa de Meia-Idade , Procedimentos Neurocirúrgicos/efeitos adversos , Artéria Cerebral Posterior/patologia , Complicações Pós-Operatórias/epidemiologia , Resultado do Tratamento , Adulto Jovem
4.
Neurol Med Chir (Tokyo) ; 51(9): 667-70, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21946735

RESUMO

A 51-year-old immunocompetent Japanese woman presented with a rare case of granulomatous amoebic encephalitis (GAE) caused by Balamuthia mandrillaris. She was brought to our hospital with epilepsy. Magnetic resonance imaging of the brain revealed a homogeneously enhanced solitary mass in the left frontal lobe. Histological diagnosis was made by a biopsy, which suggested lymphomatoid granulomatosis. After that, her neurological condition got worse. New masses were found and had spread across the whole brain. She died 2 months later of cerebral hernia. Autopsy revealed that the patient had GAE caused by Balamuthia mandrillaris. GAE is usually fatal, and is difficult to diagnose except at autopsy. Therefore, awareness of this disease is important, and earlier diagnosis and the development of a better therapeutic strategy will improve clinical outcome.


Assuntos
Amebíase/parasitologia , Balamuthia mandrillaris/isolamento & purificação , Infecções Protozoárias do Sistema Nervoso Central/parasitologia , Encefalite/parasitologia , Granuloma/parasitologia , Doenças dos Trabalhadores Agrícolas/etiologia , Doenças dos Trabalhadores Agrícolas/parasitologia , Amebíase/etiologia , Animais , Infecções Protozoárias do Sistema Nervoso Central/diagnóstico , Infecções Protozoárias do Sistema Nervoso Central/etiologia , Encefalite/etiologia , Evolução Fatal , Feminino , Granuloma/etiologia , Humanos , Japão , Pessoa de Meia-Idade
5.
J Dermatol ; 38(6): 575-80, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21366675

RESUMO

We present a case of Epstein-Barr virus (EBV)-associated primary central nervous system lymphoma (PCNSL) arising from a patient with cutaneous-type adult T-cell leukemia/lymphoma (ATLL). Extranodal sites affected by ATLL include the skin, lung, liver, gastrointestinal tract and central nervous system (CNS). CNS involvement usually occurs as an acute and lymphoma-type ATLL. PCNSL is a rare type of tumor and the vast majority of PCNSL are of B-cell lineage. Individuals with acquired, iatrogenic or congenital immunodeficiency are at increased risk of PCNSL, which is commonly associated with EBV. In our patient, the expression of latent infection membrane protein 1 (LMP1), EBV nuclear antigen 2 (EBNA2), and EBV-encoded small RNA (EBER) in tumor cells confirmed a type III latency of EBV infection. Human T-cell lymphotropic virus type I (HTLV-I) can induce immunodeficiency before the overt development of ATLL. The HTLV-I infection led to suppression of the immune system and the development of EBV-associated PCNSL. This is the first reported case of the clinicopathological features of EBV-associated PCNSL arising from a patient with ATLL.


Assuntos
Neoplasias Encefálicas/virologia , Infecções por Vírus Epstein-Barr/complicações , Infecções por HTLV-I/complicações , Leucemia-Linfoma de Células T do Adulto/virologia , Linfoma/virologia , Segunda Neoplasia Primária , Neoplasias Encefálicas/patologia , Evolução Fatal , Humanos , Linfoma/patologia , Masculino , Pessoa de Meia-Idade
6.
Childs Nerv Syst ; 23(4): 459-63, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16951962

RESUMO

CASE REPORT: We report a complicated extremely low-birth-weight (ELBW) infant with posthemorrhagic hydrocephalus after intraventricular hemorrhage and preceding stoma creation after bowel perforation who was treated with staged operations, including shunting and external ventricular drainage. The first operation was a temporary valveless ventriculoperitoneal (VP) shunt placement until the time of the stoma closure. The stoma was successfully closed 3 months after the first operation when the peritoneal tube was drawn out from the chest wall and the VP shunt system was temporarily used as an external drainage with a long subcutaneous tunnel. One month after the second operation, final VP shunt placement was performed after good healing of bowel anastomosis was surely confirmed. The previous peritoneal shunt tube was cut behind the ear, removed, and replaced with a valve-regulated VP shunt system. CONCLUSION: This staged strategy is a safe and feasible option for complicated ELBW infants with preceding stoma and hydrocephalus.


Assuntos
Hidrocefalia/cirurgia , Perfuração Intestinal/etiologia , Hemorragias Intracranianas/cirurgia , Estomas Cirúrgicos , Derivação Ventriculoperitoneal/efeitos adversos , Feminino , Humanos , Hidrocefalia/diagnóstico por imagem , Recém-Nascido de Peso Extremamente Baixo ao Nascer , Recém-Nascido , Hemorragias Intracranianas/diagnóstico por imagem , Gravidez , Ultrassonografia
7.
Pathol Int ; 55(6): 348-52, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15943792

RESUMO

An unusual case of glioblastoma with adenoid structures arising in a 30-year-old Japanese woman with neurofibromatosis type-1 (NF1) is reported. The patient was admitted to University of Miyazaki Hospital, complaining of headache, nausea and vomiting. From the neuroradiological findings the patient was diagnosed as having glioblastoma, and the tumor was surgically resected. Histologically, the tumor consisted mainly of dark basophilic cells showing prominent tubular or glandular structures surrounded by large eosinophilic cells, in addition to the typical glioblastoma features in the periphery of the tumor. Both cells showed strong stainability with glial fibrillary acidic protein (GFAP) and S-100 protein immunohistochemically, so that the tumor was classified as adenoid glioblastoma. Several cases of glioblastoma have been reported to reveal the adenoid or epithelioid differentiation. The patients with NF1 are prone to develop malignant tumors including glioblastoma, but no cases representing adenoid glioblastoma associated with NF1 have been reported. This report is considered to be the first case of adenoid glioblastoma arising in a patient with NF1. The recognition of the existence of epithelial features of glioblastoma would be important in differential diagnosis of epithelioid tumors of the brain including metastatic carcinomas.


Assuntos
Neoplasias Encefálicas/patologia , Glioblastoma/patologia , Neurofibromatose 1/patologia , Adulto , Neoplasias Encefálicas/etiologia , Neoplasias Encefálicas/metabolismo , Diagnóstico Diferencial , Feminino , Proteína Glial Fibrilar Ácida/análise , Glioblastoma/etiologia , Glioblastoma/metabolismo , Cefaleia/etiologia , Humanos , Imuno-Histoquímica , Imageamento por Ressonância Magnética , Náusea/etiologia , Neurofibromatose 1/complicações , Proteínas S100/análise , Vômito/etiologia
8.
J Neurosurg ; 99(1 Suppl): 121-4, 2003 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12859072

RESUMO

The authors devised a paramedian transmuscular approach to the C2-3 facet joint that enabled total removal of C-3 dumbbell-type neurofibroma; dissection of the paravertebral muscles from the spinous process was not required and the facet joint was preserved. Only splitting or retraction of the paravertebral muscles was necessary. The anatomical features and procedures involved in muscle splitting are described.


Assuntos
Vértebras Cervicais/cirurgia , Neurofibroma/cirurgia , Procedimentos Ortopédicos/métodos , Neoplasias da Medula Espinal/cirurgia , Adulto , Feminino , Humanos
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