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1.
J Clin Neurosci ; 20(3): 440-5, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23312560

RESUMO

The purpose of this retrospective study was to identify preoperative imaging characteristics and surgical findings that predict pain relief after microvascular decompression (MVD) for trigeminal neuralgia (TN). This study included 141 patients with follow-up ranging from 6 months to 10 years (mean follow-up=26.3 months). Preoperative images were assessed in 90 patients who were evaluated with constructive interference in steady-state (CISS) MRI in the last 6 years. These findings were compared with the severity of neurovascular conflict (NVC) found at operation to identify imaging findings useful for prognosis. Using Kaplan-Meier analysis, we found that the success rate of MVD was 91.1 ± 2.5% at 1 year and was 76.3 ± 7.5% after 5 years. A higher degree of NVC at operation (p=0.000), no vein compression (p=0.049) and single vessel compression (p=0.000) were good prognostic factors for pain relief. Two meaningful positive MRI findings, specifically, the "cerebrospinal fluid rim sign" and the "deviation sign" were statistically significantly associated with the severity of NVC at operation and MVD success (p=0.000). In this study, 34 patients (24.1%) complained of facial numbness postoperatively, and the oral herpes simplex virus was reactivated in 19 patients (13.4%). The involvement of a single arterial offender in NVC is the most important prognostic factor for MVD in TN, and the positive MRI findings described in this report may be helpful in selecting patients for MVD.


Assuntos
Cirurgia de Descompressão Microvascular , Doenças do Nervo Trigêmeo/patologia , Doenças do Nervo Trigêmeo/cirurgia , Adolescente , Adulto , Idoso , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Prognóstico , Estudos Retrospectivos , Resultado do Tratamento , Adulto Jovem
2.
J Korean Neurosurg Soc ; 52(6): 541-6, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23346326

RESUMO

OBJECTIVE: The prefabrication of customized cranioplastic implants has been introduced to overcome the difficulties of intra-operative implant molding. The authors present a new technique, which consists of the prefabrication of implant molds using three-dimensional (3D) printers and polymethyl-methacrylate (PMMA) casting. METHODS: A total of 16 patients with large skull defects (>100 cm(2)) underwent cranioplasty between November 2009 and April 2011. For unilateral cranial defects, 3D images of the skull were obtained from preoperative axial 1-mm spiral computed tomography (CT) scans. The image of the implant was generated by a digital subtraction mirror-imaging process using the normal side of the cranium as a model. For bilateral cranial defects, precraniectomy routine spiral CT scan data were merged with postcraniectomy 3D CT images following a smoothing process. Prefabrication of the mold was performed by the 3D printer. Intraoperatively, the PMMA implant was created with the prefabricated mold, and fit into the cranial defect. RESULTS: The median operation time was 184.36±26.07 minutes. Postoperative CT scans showed excellent restoration of the symmetrical contours and curvature of the cranium in all cases. The median follow-up period was 23 months (range, 14-28 months). Postoperative infection was developed in one case (6.2%) who had an open wound defect previously. CONCLUSION: Customized cranioplasty PMMA implants using 3D printer may be a useful technique for the reconstruction of various cranial defects.

3.
Exp Mol Med ; 43(12): 653-9, 2011 Dec 31.
Artigo em Inglês | MEDLINE | ID: mdl-21918363

RESUMO

In an oxygen-depleted environment, endothelial cells initiate an adaptive pattern of synthesis, which may enable them to survive hypoxic crises. Using high-resolution two-dimensional gel electrophoresis in conjunction with mass spectroscopy, we obtained a 24 differential display of proteins in the pancreatic endothelial cell line, MS-1, at four time points following induction of hypoxia. The induction of Wee1 under hypoxia was confirmed both at the mRNA and protein levels. The phosphorylation of cell division cycle 2, which is downstream of Wee1, was also increased after hypoxic exposure. In addition, pre-exposure to hypoxia attenuated a decrease in hydrogen peroxide-induced cell number. The induction of bax (a pro-apoptotic protein) and reduction of bcl (an anti-apoptotic protein) after hypoxia stimulus were also attenuated by hypoxic pre-exposure. Moreover, hydrogen peroxide-induced morphologic damage did not appear in the wild-type Wee1-expressing cells. Taken together, our results suggest that Wee1 may have important role in hypoxia- induced pathophysiological situations in endothelial cells.


Assuntos
Proteínas de Ciclo Celular/genética , Células Endoteliais/metabolismo , Regulação da Expressão Gênica , Peróxido de Hidrogênio/metabolismo , Proteínas Nucleares/genética , Proteínas Tirosina Quinases/genética , Animais , Proteína Quinase CDC2/metabolismo , Proteínas de Ciclo Celular/metabolismo , Hipóxia Celular , Linhagem Celular , Sobrevivência Celular , Células Endoteliais/citologia , Camundongos , Proteínas Nucleares/metabolismo , Pâncreas/citologia , Fosforilação , Proteínas Tirosina Quinases/metabolismo
4.
J Korean Neurosurg Soc ; 47(6): 477-9, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20617099

RESUMO

A case of delayed progressive extradural pneumatocele after microvascular decompression (MVD) is presented. A 60-year-old male underwent MVD for hemifacial spasm; the mastoid air cell was opened and sealed with bone wax during surgery. One month after surgery, the patient complained of tinnitus, and progressive extradural pneumatoceles without cerebrospinal fluid (CSF) leakage was observed. Revision surgery was performed and the opened mastoid air cell was completely sealed with muscle patch and glue. The patient's symptoms were resolved, with no recurrence of pneumatoceles at 6 month follow up. Progressive extradural pneumatocele without CSF leakage after posterior fossa surgery is a very rare complication. Previous reports and surgical management of this rare complication are discussed.

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