Radio-pathologic correlation: no pial angioma-subarachnoid varicose network drainage pathway in Sturge-Weber syndrome.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY
Child's Nervous System Pub Date : 2024-09-01 Epub Date: 2024-06-12 DOI:10.1007/s00381-024-06490-w
Shyam Sunder B Venkatakrishna, Angela N Viaene, Carmen Rosa Cerron-Vela, Onur Simsek, Adarsh Ghosh, Simon M Clifford, Savvas Andronikou
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引用次数: 0

Abstract

Purpose: The traditional imaging findings reported in Sturge-Weber syndrome (SWS) include endpoints of cortical injury-cortical atrophy and cortical calcifications-but also what has been termed a "leptomeningeal angiomatosis," the latter recognized and reported as a leptomeningeal enhancement on magnetic resonance imaging (MRI). The objective of this study is to demonstrate through neuropathological correlation that the "leptomeningeal angiomatosis" in patients with Sturge-Weber syndrome (SWS), represents a re-opened primitive venous network in the subarachnoid space that likely acts as an alternative venous drainage pathway, seen separately to abnormal pial enhancement.

Materials and methods: Retrospective review of MR imaging and surgical pathology of patients that underwent surgery for epilepsy at a tertiary, children's hospital. A pediatric radiologist with more than 20 years of experience reviewed the MR imaging. Surgically resected brain specimens that had been sectioned and fixed in 10% paraformaldehyde for histologic processing, following processing and paraffin embedding, were cut into 5-µm unstained slides which were subsequently stained with hematoxylin and eosin (H&E). Slides were re-examined by a board-certified pediatric neuropathologist, and histologic features specifically relating to cerebral surface and vascularity were documented for correlation with MR imaging of the resected region performed prior to resection.

Results: Five patients were reviewed (3 boys and 2 girls; the median age at the onset of seizures was 12 months (IQR, 7 to 45 months); the median age at surgery was 33 months (IQR, 23.5 to 56.5 months)). Surgical procedures included the following: 4, hemispherotomy (right: 2, left: 2) and 1, hemispherectomy (right). A subarachnoid space varicose network was present on both MRI and histology in 4 patients. Calcifications were seen on both MRI and histology in 3 patients. Abnormal leptomeningeal enhancement was present in 5 patients and seen separately from the subarachnoid vascular network in 4 patients.

Conclusion: Histopathology confirmed the MRI findings of a subarachnoid space varicose network seen separately from leptomeningeal enhancement and presumed to represent an alternative venous drainage pathway to compensate for maldevelopment of cortical veins, the primary abnormality in SWS. No pial-based angioma was identified.

Abstract Image

放射病理学相关性:Sturge-Weber 综合征无髓质血管瘤-蛛网膜下腔曲张网引流途径。
目的:Sturge-Weber 综合征(SWS)的传统影像学检查结果包括皮质损伤的终点--皮质萎缩和皮质钙化,但也包括所谓的 "脑膜外血管瘤病",后者在磁共振成像(MRI)上被确认并报告为脑膜外增强。本研究的目的是通过神经病理学相关性证明,Sturge-Weber 综合征(SWS)患者的 "脑膜外血管瘤病 "是蛛网膜下腔重新开放的原始静脉网络,很可能充当替代性静脉引流途径,与异常的髓腔强化不同:对一家三级儿童医院接受癫痫手术的患者的磁共振成像和手术病理进行回顾性研究。一位拥有 20 多年经验的儿科放射科医生对磁共振成像进行了复查。手术切除的脑标本经切片并用10%多聚甲醛固定后进行组织学处理,处理和石蜡包埋后切成5微米的未染色切片,随后用苏木精和伊红(H&E)染色。切片由获得认证的儿科神经病理学家重新检查,并记录与脑表面和血管有关的组织学特征,以便与切除前对切除区域进行的磁共振成像进行比对:五名患者(3 名男孩和 2 名女孩;癫痫发作时的中位年龄为 12 个月(IQR,7 至 45 个月);手术时的中位年龄为 33 个月(IQR,23.5 至 56.5 个月))接受了复查。手术程序包括以下几种:4例半球切除术(右侧:2例,左侧:2例)和1例半球切除术(右侧)。4 名患者的磁共振成像和组织学检查均显示蛛网膜下腔曲张网。3 名患者的核磁共振成像和组织学检查均显示有钙化。5名患者的脑膜异常强化,4名患者的脑膜异常强化与蛛网膜下腔血管网分开显示:组织病理学证实了 MRI 发现的蛛网膜下腔曲张网络与脑膜强化是分开的,并推测这是一种替代性静脉引流途径,用于补偿皮质静脉发育不良,而皮质静脉发育不良是 SWS 的主要异常。未发现基于髓质的血管瘤。
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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.
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