lateral ventricular

侧脑室
  • 文章类型: Journal Article
    未经证实:侧室异位神经鞘瘤(LVES)极为罕见,到目前为止,只有23例报告。本研究旨在更好地了解该病。
    未经证实:我们报道了一例罕见的LVES病例,病人被送进我们医院,对LVES的相关文献进行总结和分析,病态,成像特点和进展。
    未经证实:在23名患者中,LVES在男性中更为常见(74%,17/23)比女性多,并且主要位于右侧(78%,18/23).临床表现的平均年龄为28岁,年龄在8到68岁之间。此外,大多数病例在组织学上是良性的,除了一例恶性肿瘤.在所有良性病例中,有2例次全切除,但随访期间未发现复发.
    未经证实:LVES的起源可能是血管周围脉络丛自主神经组织的肿瘤转化。对于侧脑室肿瘤,这是罕见的良性病变,手术切除后预后良好,在鉴别诊断中应考虑LVES。此外,LVES是否可以考虑伽玛刀治疗,类似于一个小的听神经瘤,需要进一步调查。
    UNASSIGNED: Cases of lateral ventricular ectopic schwannomas (LVES) are extremely rare, with only 23 cases reported thus far. This study aimed to obtain a better understanding of the disease.
    UNASSIGNED: We reported a rare case of LVES, in which the patient was admitted to our hospital, and reviewed the relevant literature on LVES to summarize and analyze the clinical manifestations, pathologies, imaging features and progress.
    UNASSIGNED: Of the 23 patients, LVES was more common in men (74%, 17/23) than in women and was mostly located on the right side (78%, 18/23). The average age at clinical presentation was 28 years, with an age range between 8 and 68 years. Moreover, most cases were histologically benign, except in one case of malignancy. In all the benign cases, there were 2 cases of subtotal resection, but no recurrence was found during follow-up.
    UNASSIGNED: The origin of LVES could be the tumor transformation of autonomic nerve tissue in the perivascular choroid plexus. For lateral ventricle tumors,which are rare benign lesions with good prognosis after surgical resection, LVES should be considered in the differential diagnosis. Moreover, whether LVES could be considered for gamma knife treatment, similar to a small acoustic neuromas,requires further investigation.
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  • 文章类型: Case Reports
    髓质上皮瘤是一种极其罕见的高度恶性和快速生长的肿瘤,发生在中枢神经系统。位于脑室的髓上皮瘤的报道很少。髓质上皮瘤常见于幼儿和青春期。在这里,我们描述了一名4岁男性髓鞘上皮瘤患者的不寻常呕吐病例,头围增大。由于头部计算机断层扫描(CT)扫描显示脑肿瘤和脑积水的迹象,和增强的磁共振成像(MRI)序列显示,在施用造影剂后,质量的异质性和蜂窝状变化增加,患者首次诊断为脉络丛乳头状瘤。做了手术开颅手术后,患者经病理检查诊断为髓上皮瘤。我们希望这项工作将提供更多的了解和了解颅内髓上皮瘤。对于发生在中枢神经系统的髓上皮瘤,放射学检查不足以明确诊断肿瘤。病理检查可明确髓上皮瘤的诊断,并与其他中枢系统肿瘤相鉴别。手术切除是一种安全有效的方法,可以延长患者的生命。然而,髓上皮瘤的预后仍然很差,需要进一步的研究来改善这种罕见疾病的诊断和治疗。
    Medulloepithelioma is an extremely rare highly malignant and rapidly growing tumor that occurs in the central nervous system. There are few reports of medulloepithelioma located in the ventricle. Medulloepithelioma is common in young children and adolescence. Herein, we described an unusual case of vomiting in a 4-year-old male patient with medulloepithelioma, presenting with enlarging head circumference. Because of computed tomography (CT) scan of the head showed signs of brain tumors and hydrocephalus, and enhanced magnetic resonance imaging (MRI) sequence showed increased heterogeneity and honeycomb-like changes on the mass after the administration of a contrast agent, the patient was first diagnosed as choroid plexus papilloma. After undergoing a surgical craniotomy, the patient was diagnosed as medulloepithelioma through pathological examination. We hope that this work will provide more understanding and knowledge of intracranial medulloepithelioma. For medulloepithelioma that occurs in the central nervous system, radiological examination is not sufficient to make a definite diagnosis of the tumor. Pathological examination can confirm the diagnosis of medulloepithelioma and distinguish it from other central system tumors. Surgical resection is a safe and effective method that can prolong the life of patients. However, the prognosis of medulloepithelioma is still poor, and further research is needed to improve the diagnosis and treatment of this rare disease.
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