• 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

1例接受类固醇治疗的神经元核内包涵体病患者出现罕见肾脏表现的病例。

A case of unusual renal manifestation in a patient with neuronal intranuclear inclusion disease treated with steroids.

作者信息

Morita Keisuke, Shinzato Takahiro, Endo Yuzo, Suzuki Makoto, Yoshida Hidefumi, Sone Jun, Nagai Kojiro

机构信息

Department of Nephrology Shizuoka General Hospital Shizuoka Japan.

Department of Diagnostic Pathology Shizuoka General Hospital Shizuoka Japan.

出版信息

Clin Case Rep. 2023 Aug 8;11(8):e7730. doi: 10.1002/ccr3.7730. eCollection 2023 Aug.

DOI:10.1002/ccr3.7730
PMID:37564608
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10410123/
Abstract

Neuronal intranuclear inclusion disease (NIID) is a progressive neurodegenerative disorder characterized by intranuclear inclusions. Kidney injury involvement and successful treatment for NIID have rarely been reported. A NIID patient developed crescentic IgA nephropathy. Steroid therapy resolved digestive symptoms and recovered renal function. Steroids are considered for concomitant symptoms of NIID.

摘要

神经元核内包涵体病(NIID)是一种以核内包涵体为特征的进行性神经退行性疾病。肾脏损伤受累及NIID的成功治疗鲜有报道。一名NIID患者发生了新月体性IgA肾病。类固醇治疗缓解了消化症状并恢复了肾功能。对于NIID的伴随症状可考虑使用类固醇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607c/10410123/c4e01feb6238/CCR3-11-e7730-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607c/10410123/143cf9f289aa/CCR3-11-e7730-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607c/10410123/7ac742e6e27b/CCR3-11-e7730-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607c/10410123/c4e01feb6238/CCR3-11-e7730-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607c/10410123/143cf9f289aa/CCR3-11-e7730-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607c/10410123/7ac742e6e27b/CCR3-11-e7730-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607c/10410123/c4e01feb6238/CCR3-11-e7730-g002.jpg

相似文献

1
A case of unusual renal manifestation in a patient with neuronal intranuclear inclusion disease treated with steroids.1例接受类固醇治疗的神经元核内包涵体病患者出现罕见肾脏表现的病例。
Clin Case Rep. 2023 Aug 8;11(8):e7730. doi: 10.1002/ccr3.7730. eCollection 2023 Aug.
2
A case of neuronal intranuclear inclusion disease associated with lupus nephritis-like nephropathy.一例与狼疮性肾炎样肾病相关的神经元核内包涵体病。
eNeurologicalSci. 2018 Jan 12;10:28-30. doi: 10.1016/j.ensci.2018.01.002. eCollection 2018 Mar.
3
Proteomic profile of nuclei containing p62-positive inclusions in a patient with neuronal intranuclear inclusion disease.神经元核内包涵体病患者中含有p62阳性包涵体的细胞核的蛋白质组学特征。
Neurobiol Dis. 2023 Feb;177:105989. doi: 10.1016/j.nbd.2023.105989. Epub 2023 Jan 5.
4
The clinical and neuroimaging features of sporadic adult-onset neuronal intranuclear inclusion disease.散发性成年起病神经元核内包涵体病的临床和神经影像学特征。
Can J Neurol Sci. 2023 Mar;50(2):243-248. doi: 10.1017/cjn.2021.514. Epub 2022 Feb 7.
5
Coexistence of neuronal intranuclear inclusion disease and amyotrophic lateral sclerosis: an autopsy case.神经元核内包涵体病合并肌萎缩侧索硬化症:一例尸检病例。
BMC Neurol. 2021 Jul 9;21(1):273. doi: 10.1186/s12883-021-02306-5.
6
The clinical and neuropathological picture of adult neuronal intranuclear inclusion disease with no radiological abnormality.成人核内包涵体病的临床和神经病理学表现无放射学异常。
Neuropathology. 2022 Jun;42(3):204-211. doi: 10.1111/neup.12792. Epub 2022 Mar 10.
7
Neuronal Intranuclear Inclusion Disease-Related Neurotrophic Keratitis: A Case Report.神经元核内包涵体病相关的神经营养性角膜炎:一例报告
Brain Sci. 2022 Jun 14;12(6):782. doi: 10.3390/brainsci12060782.
8
Clinicopathological features of neuronal intranuclear inclusion disease diagnosed by skin biopsy.经皮肤活检诊断的神经元核内包涵体病的临床病理特征。
Neurol Sci. 2022 Mar;43(3):1809-1815. doi: 10.1007/s10072-021-05526-2. Epub 2021 Aug 13.
9
Multiple reversible encephalitic attacks: a rare manifestation of neuronal intranuclear inclusion disease.多发性可复发性脑炎样发作:神经元核内包涵体病的一种罕见表现。
BMC Neurol. 2020 Apr 8;20(1):125. doi: 10.1186/s12883-020-01712-5.
10
Clinical characteristics of two patients with neuronal intranuclear inclusion disease and literature review.两名神经元核内包涵体病患者的临床特征及文献复习
Front Neurosci. 2022 Dec 5;16:1056261. doi: 10.3389/fnins.2022.1056261. eCollection 2022.

引用本文的文献

1
A family with neuronal intranuclear inclusion disease with focal segmental glomerulosclerosis.一个家族性神经元核内包涵体病伴局灶节段性肾小球硬化症。
J Neurol. 2024 Sep;271(9):6227-6237. doi: 10.1007/s00415-024-12593-w. Epub 2024 Jul 30.
2
Adult-onset neuronal intranuclear inclusion disease presenting with acute encephalitis-like episode and without characteristic hyperintensities on MR-DWI: a case report.成人起病的神经元核内包涵体病伴急性脑炎样发作且磁共振扩散加权成像无特征性高信号:一例报告
Neurol Sci. 2024 Oct;45(10):5091-5096. doi: 10.1007/s10072-024-07630-5. Epub 2024 Jun 9.

本文引用的文献

1
Imaging findings and pathological correlations of subacute encephalopathy with neuronal intranuclear inclusion disease-Case report.亚急性脑病合并神经元核内包涵体病的影像学表现及病理相关性——病例报告
Radiol Case Rep. 2022 Sep 26;17(12):4481-4486. doi: 10.1016/j.radcr.2022.08.084. eCollection 2022 Dec.
2
Clinical and mechanism advances of neuronal intranuclear inclusion disease.神经元核内包涵体病的临床与机制进展
Front Aging Neurosci. 2022 Sep 13;14:934725. doi: 10.3389/fnagi.2022.934725. eCollection 2022.
3
First detailed case report of a pediatric patient with neuronal intranuclear inclusion disease diagnosed by NOTCH2NLC genetic testing.
首例通过NOTCH2NLC基因检测确诊的神经元核内包涵体病儿科患者的详细病例报告。
Brain Dev. 2023 Jan;45(1):70-76. doi: 10.1016/j.braindev.2022.09.002. Epub 2022 Sep 21.
4
Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy.成年起病的非血管性脑白质病伴神经元核内包涵体病。
Brain. 2022 Sep 14;145(9):3010-3021. doi: 10.1093/brain/awac135.
5
The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review.NOTCH2NLC相关GGC重复序列扩增疾病的表型与机制:综述
Mol Neurobiol. 2022 Jan;59(1):523-534. doi: 10.1007/s12035-021-02616-2. Epub 2021 Oct 31.
6
GGC Repeat Expansion of in Taiwanese Patients With Inherited Neuropathies.在台湾遗传性神经病变患者中 GGC 重复扩展。
Neurology. 2022 Jan 11;98(2):e199-e206. doi: 10.1212/WNL.0000000000013008. Epub 2021 Oct 21.
7
Fibroblasts: Origins, definitions, and functions in health and disease.成纤维细胞:起源、定义及在健康和疾病中的功能。
Cell. 2021 Jul 22;184(15):3852-3872. doi: 10.1016/j.cell.2021.06.024.
8
NOTCH2NLC Intermediate-Length Repeat Expansions Are Associated with Parkinson Disease.NOTCH2NLC中间长度重复序列扩增与帕金森病相关。
Ann Neurol. 2021 Jan;89(1):182-187. doi: 10.1002/ana.25925. Epub 2020 Oct 19.
9
Identification of GGC repeat expansion in the gene in amyotrophic lateral sclerosis.肌萎缩侧索硬化症中 基因的 GGC 重复扩展的鉴定。
Neurology. 2020 Dec 15;95(24):e3394-e3405. doi: 10.1212/WNL.0000000000010945. Epub 2020 Sep 28.
10
Association of NOTCH2NLC Repeat Expansions With Parkinson Disease.NOTCH2NLC 重复扩展与帕金森病的关联。
JAMA Neurol. 2020 Dec 1;77(12):1559-1563. doi: 10.1001/jamaneurol.2020.3023.