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儿童大脑外侧裂脑膜瘤:3例报告并文献复习

Sylvian Fissure Meningioma in Childhood: Report of 3 Cases and Review of the Literature.

作者信息

Amirjamshidi Abbas, Khalatbari Mahmoud Reza, Abbasioun Kazem, Ghasemi Babak

机构信息

Department of Neurosurgery, Sina Hospital and Children's Hospital Medical Center, Tehran University of Medical Sciences (TUMS), Tehran, Iran,

Department of Neurosurgery, Arad Hospital, Tehran, Iran.

出版信息

Pediatr Neurosurg. 2019;54(4):270-276. doi: 10.1159/000500765. Epub 2019 Jun 25.

Abstract

OBJECTIVE

Sylvian fissure-based meningioma is a rare occurrence during childhood. We report a small series including 3 such cases, all attached to the arachnoid leaflets of the Sylvian fissure. We present a review of the literature and discuss the impact of possibly effective clinical, imaging, and surgical variables on the outcome.

METHODS

In a retrospective chart review of children with intracranial meningioma, we encountered 3 cases with Sylvian fissure meningioma operated within the past 32 years.

RESULTS

Two girls, 5 and 7 years old, and 1 boy, 7 years of age, presented with epilepsy, headache, diplopia, and hemiparesis. The duration of illness was 3, 4, and 2 months, respectively. All three tumors were attached to the arachnoid layer of the adjacent Sylvian fissure, and they were not dural based. Gross total resection could be achieved, and no recurrences were encountered after 13, 7, and 2 years.

CONCLUSION

We report 3 very rare cases of Sylvian arachnoid-based meningiomas. To our knowledge, this is the study with the longest follow-up period (mean 7.3 years, median 7 years). Even though the overall prognosis of pediatric meningiomas may be worse than that of adult illness, we would like to emphasize that the "rare location" of the Sylvian fissure was not an important factor contributing to the outcome in our children.

摘要

目的

基于外侧裂的脑膜瘤在儿童期较为罕见。我们报告一小系列包含3例此类病例,所有病例均附着于外侧裂的蛛网膜小叶。我们对文献进行综述,并讨论可能有效的临床、影像学及手术变量对预后的影响。

方法

在对颅内脑膜瘤患儿进行回顾性病历审查时,我们遇到3例在过去32年内接受手术的外侧裂脑膜瘤病例。

结果

两名女孩,分别为5岁和7岁,以及一名7岁男孩,表现为癫痫、头痛、复视和偏瘫。病程分别为3个月、4个月和2个月。所有三个肿瘤均附着于相邻外侧裂的蛛网膜层,并非硬膜型。实现了肿瘤全切,在13年、7年和2年后均未出现复发。

结论

我们报告3例非常罕见的基于外侧裂蛛网膜的脑膜瘤病例。据我们所知,这是随访期最长(平均7.3年,中位数7年)的研究。尽管儿童脑膜瘤的总体预后可能比成人疾病更差,但我们想强调外侧裂的“罕见位置”并非影响我们这些患儿预后的重要因素。

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