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一名患有视网膜血管病变伴脑白质脑病及全身表现的患者出现脑水肿导致镰下疝和钩回疝

"Cerebral Edema Leading to Subfalcine and Uncal Herniation in a Patient With Retinal Vasculopathy With Cerebral Leukoencephalopathy and Systemic Manifestations".

作者信息

Hughes Parker, Lu Liang, Shi Michael, Syed Danial

机构信息

Department of Neurology, Baylor College of Medicine, Houston, TX, USA.

Department of Medicine, Baylor College of Medicine, Houston, TX, USA.

出版信息

Neurohospitalist. 2024 Dec 20:19418744241310473. doi: 10.1177/19418744241310473.

DOI:10.1177/19418744241310473
PMID:39712866
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11662338/
Abstract

Deterioration of a patient's state of consciousness is among the most concerning signs encountered in clinical practice. The evaluation of this finding carries a broad initial differential diagnosis and must account for any relevant medical history. We describe the case of a 41-year-old male with known retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (RVCL-S) who presented with progressive mental status decline and acute onset intractable headache. Head computed tomography (CT) revealed extensive vasogenic edema, resulting in right to left shift of 11 millimeters at the level of the lateral ventricles, with associated uncal and subfalcine herniation. He was treated with a 5-day course of methylprednisolone, leading to resolution of his lethargy and headache. Follow up neuroimaging with magnetic resonance (MRI) brain demonstrated interval improvement with the midline shift reduced to 3 millimeters after completion of high dose corticosteroids. Neurosurgical intervention was considered, but ultimately not required given his improvement. This case describes the management of life-threatening cerebral edema as a complication of RVCL-S disease progression. Due to the rarity of this disease, there are no standardized guidelines for treatment and the care for such patients relies on expert opinion, case studies, and extrapolation of principles learned from related conditions. Our intention is that the reporting of this case will contribute to the limited body of literature and aid those affected by this condition.

摘要

患者意识状态恶化是临床实践中最令人担忧的体征之一。对这一发现的评估存在广泛的初步鉴别诊断,并且必须考虑任何相关的病史。我们描述了一名41岁男性的病例,他患有已知的伴有脑白质脑病和全身表现的视网膜血管病变(RVCL-S),出现进行性精神状态下降和急性发作的顽固性头痛。头部计算机断层扫描(CT)显示广泛的血管源性水肿,导致侧脑室水平从右向左移位11毫米,并伴有钩回和大脑镰下疝。他接受了为期5天的甲泼尼龙治疗,嗜睡和头痛症状得到缓解。后续的脑部磁共振成像(MRI)显示,在完成高剂量皮质类固醇治疗后,中线移位减少至3毫米,病情有阶段性改善。曾考虑进行神经外科干预,但鉴于他的病情改善,最终未实施。本病例描述了作为RVCL-S疾病进展并发症的危及生命的脑水肿的管理。由于这种疾病罕见,没有标准化的治疗指南,对此类患者的护理依赖专家意见、病例研究以及从相关病症中学到的原则的推断。我们希望本病例报告将为有限的文献做出贡献,并帮助那些受此病影响的人。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f2/12099109/d7f8dabba3b1/10.1177_19418744241310473-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f2/12099109/b396210772e5/10.1177_19418744241310473-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f2/12099109/d7f8dabba3b1/10.1177_19418744241310473-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f2/12099109/b396210772e5/10.1177_19418744241310473-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f2/12099109/d7f8dabba3b1/10.1177_19418744241310473-fig2.jpg

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本文引用的文献

1
Retinal Vasculopathy With Cerebral Leukodystrophy: Clinicopathologic Features of an Autopsied Patient With a Heterozygous TREX 1 Mutation.伴有脑白质营养不良的视网膜血管病:一例经尸检证实的 TREX1 杂合突变患者的临床病理特征。
J Neuropathol Exp Neurol. 2019 Feb 1;78(2):181-186. doi: 10.1093/jnen/nly115.
2
Retinal vasculopathy with cerebral leukoencephalopathy (RVCL): A rare mimic of tumefactive MS.视网膜血管病变伴脑白质病(RVCL):一种罕见的肿块样多发性硬化症模拟疾病。
Neurology. 2018 Oct 9;91(15):e1423-e1428. doi: 10.1212/WNL.0000000000006329. Epub 2018 Sep 7.
3
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations.
伴有脑白质病和全身表现的视网膜血管病变。
Brain. 2016 Nov 1;139(11):2909-2922. doi: 10.1093/brain/aww217.
4
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy.人类3'-5' DNA核酸外切酶TREX1的C末端截短会导致伴有脑白质营养不良的常染色体显性视网膜血管病变。
Nat Genet. 2007 Sep;39(9):1068-70. doi: 10.1038/ng2082. Epub 2007 Jul 29.
5
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.遗传性血管性视网膜病变、脑视网膜血管病变以及伴有视网膜病变、肾病和中风的遗传性内皮病变定位于3号染色体p21.1 - p21.3的一个单一基因座。
Am J Hum Genet. 2001 Aug;69(2):447-53. doi: 10.1086/321975. Epub 2001 Jun 28.
6
Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS).伴有视网膜病变、肾病和中风的遗传性内皮病(HERNS)。
Neurology. 1997 Nov;49(5):1322-30. doi: 10.1212/wnl.49.5.1322.