Synchronous intracranial arteriovenous malformation and papillary glioneuronal tumour: hypothesis or reality?

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY
Michael Stuart, Adam Burnett, Thomas Robertson, Annabelle Harbison, Liam Coulthard, Robert Campbell
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引用次数: 0

Abstract

Brain arteriovenous malformations (AVM) rarely occur with spatial and/or temporal co-localisation to intracranial neoplasms. Most prior reports describe this association with high-grade gliomas; however, reports of a co-occurrence with low grade gliomas are very rare. It is unclear whether such cases represent a true co-occurrence of separate pathologies or simply an unusually vascular phenotype of the neoplasm. Most such reports pre-date the era of molecularly defined gliomas. We present the first report of the spatial and temporal co-occurrence of an intracranial arteriovenous malformation traversing and within a papillary glioneuronal tumour, molecularly defined by the presence of SLC44A1::PRKCA fusion. This case was successfully managed by resection of both lesions adhering to the principles of AVM surgery. It is possible these exceptionally rare co-occurrences may have common underlying molecular drivers relating to the mitogen activated protein kinase (MAPK) pathway.

Abstract Image

颅内动静脉畸形和乳头状胶质细胞瘤的同步性:假设还是现实?
脑动静脉畸形(AVM)很少与颅内肿瘤在空间和/或时间上同时发生。之前的大多数报告都描述了这种与高级别胶质瘤的关联;然而,与低级别胶质瘤同时发生的报告却非常罕见。目前还不清楚这些病例是代表不同病理的真正共存,还是仅仅代表肿瘤的异常血管表型。大多数此类报告都是在胶质瘤分子定义时代之前出现的。我们首次报道了颅内动静脉畸形穿越乳头状胶质瘤并在乳头状胶质瘤内同时存在的空间和时间上的并发症,其分子定义是存在SLC44A1::PRKCA融合。该病例按照动静脉畸形手术原则,成功切除了两个病灶。这些异常罕见的并发症可能具有与丝裂原活化蛋白激酶(MAPK)通路有关的共同潜在分子驱动因素。
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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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