• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在一例患有伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)患者的腓肠神经活检中鉴定特征性血管变化。

Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

作者信息

Schröder J M, Sellhaus B, Jörg J

机构信息

Institute of Neuropathology, Medical Faculty, Technical University Aachen, Germany.

出版信息

Acta Neuropathol. 1995;89(2):116-21. doi: 10.1007/BF00296354.

DOI:10.1007/BF00296354
PMID:7732783
Abstract

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy' (CADASIL) has recently been identified as a hereditary disorder with characteristic fine structural changes of small intracerebral arteries and arterioles. Electron microscopically there are characteristic perivascular deposits of granular electron-dense material resembling immunoglobulin deposits. The present case from a family with four affected members in three successive generations shows that similar vascular changes as described in the central nervous system are present in blood vessels of the sural nerve, although less pronounced and, therefore, affording electron microscopy for their unequivocal detection. Nevertheless it has been shown for the first time that the diagnosis of CADASIL can be verified by a sural nerve biopsy. Occasional focal accumulation of pinocytotic vesicles opposite the granular deposits suggests exocytosis as one of the possible pathomechanisms for their production.

摘要

伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)最近被确认为一种遗传性疾病,其特征是脑内小动脉和微动脉有细微的结构变化。在电子显微镜下,有特征性的血管周围颗粒状电子致密物质沉积,类似于免疫球蛋白沉积。本病例来自一个连续三代中有四名患病成员的家族,结果显示,腓肠神经血管中存在与中枢神经系统中所描述的相似的血管变化,尽管不太明显,因此需要借助电子显微镜才能明确检测到这些变化。然而,首次证明通过腓肠神经活检可以确诊CADASIL。在颗粒状沉积物相对的位置偶尔出现的局灶性胞饮小泡聚集提示胞吐作用是其产生的可能发病机制之一。

相似文献

1
Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).在一例患有伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)患者的腓肠神经活检中鉴定特征性血管变化。
Acta Neuropathol. 1995;89(2):116-21. doi: 10.1007/BF00296354.
2
A patient with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) confirmed by sural nerve biopsy.一名经腓肠神经活检确诊为伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)的患者。
J Neurol Neurosurg Psychiatry. 1996 Feb;60(2):235-6. doi: 10.1136/jnnp.60.2.235.
3
Skin and sural nerve biopsies: ultrastructural findings in the first genetically confirmed cases of CADASIL in Serbia.皮肤和腓肠神经活检:塞尔维亚首例基因确诊的大脑常染色体显性动脉病伴皮质下梗死和白质脑病(CADASIL)病例的超微结构发现
Ultrastruct Pathol. 2012 Oct;36(5):325-35. doi: 10.3109/01913123.2012.679352.
4
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family.伴有皮质下梗死和白质脑病的大脑常染色体显性动脉病:一个瑞士家族的临床病理及遗传学研究
J Neurol Neurosurg Psychiatry. 1995 Aug;59(2):138-43. doi: 10.1136/jnnp.59.2.138.
5
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)--confirmation by cerebral biopsy in 2 cases.伴有皮质下梗死和白质脑病的脑常染色体显性动脉病(CADASIL)——2例经脑活检确诊
Clin Neuropathol. 1995 Jul-Aug;14(4):201-6.
6
CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): diagnostic skin biopsy changes determined by electron microscopy.
J Am Acad Dermatol. 2000 Dec;43(6):1125-7. doi: 10.1067/mjd.2000.110895.
7
Vasculopathic changes of CADASIL can be focal in skin biopsies.
Ultrastruct Pathol. 1999 Jul-Aug;23(4):241-7. doi: 10.1080/019131299281572.
8
Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).脑常染色体显性遗传性动脉病伴皮质下梗死和白质脑病(CADASIL)中的肾脏受累情况。
Clin Nephrol. 2007 Mar;67(3):182-7. doi: 10.5414/cnp67182.
9
Peripheral neuropathy in CADASIL.
J Neurol. 2005 Oct;252(10):1206-9. doi: 10.1007/s00415-005-0837-5. Epub 2005 Apr 15.
10
[Dominant autosomal cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). A review].
Neurologia. 2002 Oct;17(8):410-7.

引用本文的文献

1
Chromosome 10q26-driven age-related macular degeneration is associated with reduced levels of in human retinal pigment epithelium.10q26 染色体驱动的年龄相关性黄斑变性与人类视网膜色素上皮中 的水平降低有关。
Proc Natl Acad Sci U S A. 2021 Jul 27;118(30). doi: 10.1073/pnas.2103617118.
2
ER stress and Rho kinase activation underlie the vasculopathy of CADASIL.脑动脉淀粉样血管病的血管病变与内质网应激和 Rho 激酶激活有关。
JCI Insight. 2019 Dec 5;4(23):131344. doi: 10.1172/jci.insight.131344.
3
Differences in proliferation rate between CADASIL and control vascular smooth muscle cells are related to increased TGFβ expression.

本文引用的文献

1
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病定位于19号染色体长臂12区。
Nat Genet. 1993 Mar;3(3):256-9. doi: 10.1038/ng0393-256.
2
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.
Stroke. 1993 Jan;24(1):122-5. doi: 10.1161/01.str.24.1.122.
3
Autosomal dominant arteriopathic leuko-encephalopathy and Alzheimer's disease.
Neuropathol Appl Neurobiol. 1994 Feb;20(1):22-30. doi: 10.1111/j.1365-2990.1994.tb00953.x.
4
CADASIL 与对照血管平滑肌细胞增殖率的差异与 TGFβ 表达增加有关。
J Cell Mol Med. 2018 Jun;22(6):3016-3024. doi: 10.1111/jcmm.13534. Epub 2018 Mar 13.
4
Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients.电子显微镜在 CADASIL 综合征诊断中的作用:32 例患者研究。
PLoS One. 2013 Jun 17;8(6):e65482. doi: 10.1371/journal.pone.0065482. Print 2013.
5
Nerve conduction studies in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.脑常染色体显性动脉病伴皮质下梗死和白质脑病的神经传导研究。
J Neurol. 2009 Oct;256(10):1724-7. doi: 10.1007/s00415-009-5191-6. Epub 2009 Jun 2.
6
Neuropsychiatric manifestations in CADASIL.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病的神经精神症状
Dialogues Clin Neurosci. 2007;9(2):199-208. doi: 10.31887/DCNS.2007.9.2/hchabriat.
7
Single gene disorders causing ischaemic stroke.导致缺血性中风的单基因疾病。
J Neurol. 2006 Jun;253(6):685-700. doi: 10.1007/s00415-006-0048-8.
8
Neuropathology of Charcot-Marie-Tooth and related disorders.夏科-马里-图斯病及相关疾病的神经病理学
Neuromolecular Med. 2006;8(1-2):23-42. doi: 10.1385/nmm:8:1-2:23.
9
Peripheral neuropathy in CADASIL.
J Neurol. 2005 Oct;252(10):1206-9. doi: 10.1007/s00415-005-0837-5. Epub 2005 Apr 15.
10
Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.表达突变Notch3的转基因小鼠出现具有大脑常染色体显性动脉病伴皮质下梗死和白质脑病特征的血管改变。
Am J Pathol. 2003 Jan;162(1):329-42. doi: 10.1016/S0002-9440(10)63824-2.
Small arterial granular degeneration in familial Binswanger's syndrome.家族性宾斯旺格综合征中的小动脉颗粒样变性
Acta Neuropathol. 1994;87(1):98-105. doi: 10.1007/BF00386260.
5
The microvascular changes in cases of hereditary multi-infarct disease of the brain.
Acta Neuropathol. 1994;87(3):317-24. doi: 10.1007/BF00296749.
6
Summary of the proceedings of the First International Workshop on CADASIL. Paris, May 19-21, 1993.第一届CADASIL国际研讨会会议纪要。巴黎,1993年5月19日至21日。
Stroke. 1994 Mar;25(3):704-7. doi: 10.1161/01.str.25.3.704.
7
Chronic progressive leukoencephalopathy with systemic arteriosclerosis in young adults.青年成人慢性进行性白质脑病伴系统性动脉硬化
Clin Neuropathol. 1985 Jul-Aug;4(4):165-73.
8
Collagens in atherosclerosis.动脉粥样硬化中的胶原蛋白
Coll Relat Res. 1985 Jan;5(1):65-97. doi: 10.1016/s0174-173x(85)80048-0.
9
Hereditary multi-infarct dementia.
Eur Neurol. 1987;27(4):209-15. doi: 10.1159/000116158.
10
Proliferation of epineurial capillaries and smooth muscle cells in angiopathic peripheral neuropathy.
Acta Neuropathol. 1986;72(1):29-37. doi: 10.1007/BF00687944.