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鞍上蛛网膜囊肿源于异位脉络丛:病例报告。

Suprasellar arachnoid cyst due to ectopic choroid plexus: case report.

机构信息

Department of Neurosurgery, University of the Witwatersrand, Johannesburg, South Africa.

Department of Paediatric Neurosurgery, Nelson Mandela Children's Hospital, 6 Jubilee Rd, Parktown, Johannesburg, 2193, South Africa.

出版信息

Childs Nerv Syst. 2022 Jul;38(7):1381-1384. doi: 10.1007/s00381-021-05395-2. Epub 2021 Oct 19.

Abstract

Arachnoid cysts (ACs) are malformations that account for about 1% of all intracranial lesions. The aetiology and progression of these lesions have been debated, with one possible explanation being the production of cerebro-spinal fluid (CSF) by ectopic choroid plexus (CP). To our knowledge, only seven cases of ACs incorporating CP have been reported, and we believe this to be the first reported case of a suprasellar AC containing ectopic CP. A 1-year-old boy presented with developmental delay and macrocephaly. MRI scan revealed hydrocephalus due to a suprasellar AC. An endoscopic ventriculocisternostomy was undertaken. Intra-operatively, intra-cystic, pink frond-like tissue resembling choroid plexus was identified. Histologically, the cyst wall was composed of fibrous tissue, with layered arachnoid cells, while the frond-like tissue was composed of papillary structures in keeping with normal choroid plexus tissue. We postulate that the rest of the ectopic CP may have been trapped within the double layered arachnoid fold of the diencephalic leaf of Liliequist's membrane which may drive the formation and development of certain suprasellar ACs.

摘要

蛛网膜囊肿 (ACs) 是一种畸形,约占所有颅内病变的 1%。这些病变的病因和进展一直存在争议,有一种可能的解释是异位脉络丛 (CP) 产生脑脊液 (CSF)。据我们所知,只有 7 例包含 CP 的 AC 病例被报道,我们认为这是首例报告的含有异位 CP 的鞍上 AC 病例。一名 1 岁男孩因发育迟缓伴大头症就诊。MRI 扫描显示由于鞍上 AC 导致的脑积水。进行了内镜脑室-脑池造瘘术。术中发现囊内呈粉红色叶状的类似脉络丛的组织。组织学上,囊肿壁由纤维组织组成,有分层的蛛网膜细胞,而叶状组织由与正常脉络丛组织一致的乳头状结构组成。我们推测,其余异位 CP 可能被困在利利奎斯特膜的间脑叶双层蛛网膜褶皱内,这可能导致某些鞍上 AC 的形成和发展。

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