枕状脑积水:手术后神经发育结果的回顾性分析和评估。

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Child's Nervous System Pub Date : 2024-12-01 Epub Date: 2024-06-24 DOI:10.1007/s00381-024-06506-5
Soumen Kanjilal, Pawan Kumar Verma, Shreyash Rai, Ashutosh Kumar, Kamlesh Singh Bhaisora, Ved Prakash Maurya, Kuntal Kanti Das, Anant Mehrotra, Arun Kumar Srivastava, Awadhesh Kumar Jaiswal
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引用次数: 0

摘要

背景:脑疝是一组疾病,其特点是颅骨结构缺陷导致颅外的脑膜、脑和脑脊液疝出。目的:本研究旨在评估手术切除枕状脑积水患者神经系统发育的预测因素:过去十年(2012-2022 年)接受手术的所有枕叶脑瘤患者。注意囊的大小、是否存在脑积水以及相关的异常情况。对这些患者的活检结果进行审查,并将其分为含有成熟神经组织和不含成熟神经组织的两类。神经系统结果通过社交、语言、认知和运动里程碑进行评估,并分为无发育迟缓、轻度(4 例中的 1 例)、中度(4 例中的 2 或 3 例)和重度发育迟缓(4 例中的 4 例):共纳入 35 名患者,中位年龄为 10 个月(IQR = 5-20 个月)。15名患者(42.9%)的囊肿大小≥5厘米,23名患者(65.7%)的活检结果显示神经组织成熟。中位随访时间为 6.4 年(IQR = 4.38-10.65 年)。17名患者(49.6%)有中度至重度发育迟缓。囊肿大小≥5 cm (AOR = 33.5; 95%CI = 3.35-334.8) (p = 0.003)和囊肿中存在成熟的神经内容物 (AOR = 13.32; 95%CI = 1.1-160.36) (p = 0.041)与明显的神经发育迟缓有关:结论:脑疝患者存在≥5厘米的大囊,且组织病理学标本中存在成熟的神经组织,这表明患者的神经系统发育可能较差。
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Occipital encephalocele: a retrospective analysis and assessment of post-surgical neurodevelopmental outcome.

Background: Encephalocele represent a group of disorders which is characterised by extracranial herniation of the leptomeninges, brain, and CSF through a structural defect in the cranium. They are usually associated with other intracranial anomalies which may impact the neurological development.

Aim: This study aimed to assess the predictors of neurological development of patients undergone surgical excision of occipital encephalocele.

Methods: All patients with occipital encephaloceles operated over the last decade (2012-2022). The sac size, presence of hydrocephalous, and associated anomalies were noted. The biopsy of these patients were reviewed and categorised as those which contains mature neural tissue and those without. The neurological outcomes were assessed by social, language, cognitive, and motor milestone and has been stratified into no delay, mild (1 of 4), moderate (2 or 3 of 4), and severe development delay (4 of 4).

Results: Total of 35 patients were included with median age of 10 months (IQR = 5-20 months). Fifteen (42.9%) patients had sac size of ≥ 5 cm, and 23 (65.7%) patients had mature neural tissues on biopsy. The median follow-up period was 6.4 years (IQR = 4.38-10.65) years. Seventeen (49.6%) patients had moderate to severe developmental delay. The sac size of ≥ 5 cm (AOR = 33.5; 95%CI = 3.35-334.8) (p = 0.003) and presence of mature neural content in the sac (AOR = 13.32; 95%CI = 1.1-160.36) (p = 0.041) were associated with significant neurodevelopmental delay.

Conclusion: The presence of a large sac of ≥ 5 cm and the presence of mature neural tissues on histopathological specimen of patients with encephalocele point towards the possibility of poor neurological development.

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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
期刊最新文献
Correction: Imaging features of pediatric meningiomas: emphasis on unusual locations. Correction: Occipital encephalocele: a retrospective analysis and assessment of post-surgical neurodevelopmental outcome. Radiographic severity is associated with worse executive function in metopic craniosynostosis. Occipital encephalocele: a retrospective analysis and assessment of post-surgical neurodevelopmental outcome. Vaulting further: cranial vault expansion for craniocerebral disproportion without primary craniosynostosis.
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