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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Clinical features and microsurgical treatment of pediatric patients with cerebral cavernous malformation.
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Clinical features and microsurgical treatment of pediatric patients with cerebral cavernous malformation.

机译:小儿脑海绵状畸形的临床特征及显微外科治疗。

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The aim of the present study was to describe the clinical features and to evaluate the surgical treatment outcomes of pediatric patients with cerebral cavernous malformations (CCM). We investigated 85 children (53 boys and 32 girls), aged from 6 months to 17.9 years with CCM. Seizures and symptomatic hemorrhages, which were the most frequent symptoms, occurred in 81 patients. Nine patients had a positive family history of CCM. Eighty patients underwent microsurgical treatment after strict operative indications were met. Neuronavigation, combined with intraoperative ultrasonography or functional MRI, was used for precise localization of the lesions. The principles of minimally invasive techniques were followed during surgery. A total of 89 lesions were removed in 80 patients, and there were no deaths. During their hospital stay, only nine patients suffered from postoperative seizures, which were controlled with medication. Postoperative neurological deficits improved in 27 patients, were unchanged in nine, and worsened in two. With the help of advanced neuroimaging, a satisfactory surgical outcome was achieved for 10 lesions located in eloquent brain areas and four lesions in the brain stem. A follow-up study of 66 patients showed that all of these patients remained seizure-free, and nine patients with postoperative neurological deficits gradually recovered. Microsurgical treatment should be performed early for pediatric patients with CCM. Accurate localization of the lesions and the use of minimally invasive techniques and functional MRI monitoring were the key features of the surgical procedures.
机译:本研究的目的是描述小儿脑海绵状畸形(CCM)的临床特征并评估其手术治疗效果。我们调查了85名年龄在6个月至17.9岁之间的CCM儿童(53名男孩和32名女孩)。抽搐和症状性出血是最常见的症状,发生在81例患者中。 9名患者的CCM家族史为阳性。符合严格的手术指征后,对80例患者进行了显微手术治疗。神经导航结合术中超声检查或功能性MRI用于精确定位病变。在手术过程中遵循了微创技术的原则。 80例患者共切除了89个病灶,没有死亡。在住院期间,只有9名患者发生了术后癫痫发作,并由药物控制。术后神经功能缺损有27例改善,9例未改变,2例恶化。借助先进的神经成像技术,位于雄辩的大脑区域的10个病变和脑干的四个病变实现了令人满意的手术效果。一项对66位患者的随访研究表明,所有这些患者均无癫痫发作,并且9位术后神经功能缺损的患者逐渐康复。小儿CCM患者应及早进行显微外科治疗。病变的准确定位以及使用微创技术和功能性MRI监测是外科手术的关键特征。

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