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儿童脑部手术后的医源性脑淀粉样血管病:MRI和CT的新发现

Iatrogenic Cerebral Amyloid Angiopathy After Childhood Brain Surgery: Novel Findings of MRI and CT.

作者信息

Tanaka Fumine, Umino Maki, Matsukawa Megumi, Kishi Seiya, Kogue Ryota, Kawada Norikazu, Kagawa Ken, Utsunomiya Takaya, Kajikawa Hiroyuki, Ishikawa Hidehiro, Ii Yuichiro, Shindo Akihiro, Sakuma Hajime, Maeda Masayuki

机构信息

Department of Radiology, Mie University School of Medicine, 2-174 Edobashi, Tsu 514-8507, Mie, Japan.

Department of Radiology, Matsusaka Chuo General Hospital, Matsusaka 515-0818, Mie, Japan.

出版信息

Neurol Int. 2025 Apr 24;17(5):64. doi: 10.3390/neurolint17050064.

DOI:10.3390/neurolint17050064
PMID:40423220
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12114373/
Abstract

: A subtype of cerebral amyloid angiopathy (CAA), iatrogenic CAA (iCAA), has been increasingly reported. iCAA occurs primarily in patients who underwent surgery during childhood and is caused by the prion-like propagation of amyloid beta. This subtype of CAA tends to develop at a younger age than age-related CAA, usually before the age of 55. After a latency period of 20-40 years following surgery, it manifests as lobar intracerebral hemorrhage (ICH), cognitive impairment, or transient focal neurological episodes. Between 2023 and 2024, we observed four cases of possible iCAA, all of which had a history of neurosurgery during childhood. : MRI findings for all cases revealed multiple lobar microbleeds. Two cases also showed cortical superficial siderosis and lobar ICH. Notably, contrast-enhanced 3D FLAIR demonstrated sulcal enhancement in two cases, and CT demonstrated cortical calcification in the bilateral posterior lobes in one case. : Sulcal enhancement on contrast-enhanced 3D FLAIR and cortical calcification in the bilateral posterior lobes on CT may suggest advanced CAA in the present cases.

摘要

医源性脑淀粉样血管病(iCAA)作为脑淀粉样血管病(CAA)的一种亚型,其报道日益增多。iCAA主要发生在童年时期接受过手术的患者中,由淀粉样β蛋白的朊病毒样传播引起。与年龄相关的CAA相比,这种CAA亚型往往在更年轻的时候发病,通常在55岁之前。在手术后20 - 40年的潜伏期后,表现为脑叶脑出血(ICH)、认知障碍或短暂性局灶性神经发作。在2023年至2024年期间,我们观察到4例可能的iCAA病例,所有病例均有童年时期神经外科手术史。所有病例的MRI表现均显示多发脑叶微出血。2例还显示皮质表面铁沉积和脑叶ICH。值得注意的是,对比增强3D FLAIR显示2例有脑沟强化,CT显示1例双侧后叶皮质钙化。对比增强3D FLAIR上的脑沟强化和CT上双侧后叶皮质钙化可能提示本病例中存在晚期CAA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2947/12114373/db108f6a2950/neurolint-17-00064-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2947/12114373/b05b275fe3c6/neurolint-17-00064-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2947/12114373/4e5e77d3284a/neurolint-17-00064-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2947/12114373/c973831d1310/neurolint-17-00064-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2947/12114373/db108f6a2950/neurolint-17-00064-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2947/12114373/b05b275fe3c6/neurolint-17-00064-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2947/12114373/4e5e77d3284a/neurolint-17-00064-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2947/12114373/c973831d1310/neurolint-17-00064-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2947/12114373/db108f6a2950/neurolint-17-00064-g004.jpg

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本文引用的文献

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J Neurol Neurosurg Psychiatry. 2025 Feb 12. doi: 10.1136/jnnp-2024-335164.
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Updated imaging markers in cerebral amyloid angiopathy: What radiologists need to know.脑淀粉样血管病的更新影像学标志物:放射科医生需要了解的内容。
Jpn J Radiol. 2025 May;43(5):736-751. doi: 10.1007/s11604-024-01720-2. Epub 2024 Dec 28.
3
A Rare Case of Iatrogenic Prion-like Pathogenesis of Cerebral Amyloid Angiopathy.
一例医源性脑淀粉样血管病类朊蛋白致病机制的罕见病例。
Dtsch Arztebl Int. 2024 Jan 26;121(2):68-69. doi: 10.3238/arztebl.m2023.0215.
4
Identifying diagnostic and prognostic factors in cerebral amyloid angiopathy-related inflammation: A systematic analysis of published and seven new cases.识别脑淀粉样血管病相关性炎症中的诊断和预后因素:已发表病例及7例新病例的系统分析
Neuropathol Appl Neurobiol. 2024 Feb;50(1):e12946. doi: 10.1111/nan.12946.
5
Rare forms of cerebral amyloid angiopathy: pathogenesis, biological and clinical features of CAA-ri and iCAA.罕见形式的脑淀粉样血管病:CAA-ri和iCAA的发病机制、生物学及临床特征
Front Neurosci. 2023 Jul 10;17:1219025. doi: 10.3389/fnins.2023.1219025. eCollection 2023.
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Case report of iatrogenic cerebral amyloid angiopathy after exposure to Lyodura: an Australian perspective.接触Lyodura后发生医源性脑淀粉样血管病的病例报告:澳大利亚视角
Front Neurosci. 2023 May 5;17:1185267. doi: 10.3389/fnins.2023.1185267. eCollection 2023.
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Iatrogenic Cerebral Amyloid Angiopathy Post Neurosurgery: Frequency, Clinical Profile, Radiological Features, and Outcome.手术后医源性脑淀粉样血管病:频率、临床特征、影像学特征和转归。
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Neurology. 2022 Sep 20;99(12):e1265-e1277. doi: 10.1212/WNL.0000000000200892. Epub 2022 Aug 8.
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The Boston criteria version 2.0 for cerebral amyloid angiopathy: a multicentre, retrospective, MRI-neuropathology diagnostic accuracy study.波士顿标准 2.0 版用于脑淀粉样血管病:一项多中心、回顾性、MRI-神经病理学诊断准确性研究。
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