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菲律宾戴克-戴维多夫-马森综合征病例报告:文献综述及神经可塑性与脑网络连接性探讨

A Case Report of Dyke-Davidoff-Masson Syndrome in the Philippines: Review of the Literature and a Discussion on Neuroplasticity and Brain Network Connectivity.

作者信息

Santos Edren Daeniel G, Mariano Geraldine Siena, Pilotin Ron, Berroya Maria Anna

机构信息

Neurology, St. Luke's Medical Center, Quezon City, PHL.

Radiology and Neuroradiology, St. Luke's Medical Center, Quezon City, PHL.

出版信息

Cureus. 2025 Mar 18;17(3):e80762. doi: 10.7759/cureus.80762. eCollection 2025 Mar.

DOI:10.7759/cureus.80762
PMID:40248536
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12005121/
Abstract

Dyke-Davidoff-Masson syndrome is a rare neurologic condition wherein there is characteristic cerebral hemiatrophy that is either congenital or acquired, with a classical presentation of seizures, hemiparesis, and cognitive impairment. Here, we have an unusual case of a young, adult female who sustained a traumatic brain injury in her childhood leading to hemiatrophy but with minimal deficits. This study also summarizes the available data and discusses neuroplasticity and brain network connectivity.

摘要

戴克-戴维多夫-马森综合征是一种罕见的神经系统疾病,其特征为先天性或后天性的典型脑半球萎缩,并伴有癫痫发作、偏瘫和认知障碍的经典表现。在此,我们报告一例不寻常的病例,一名年轻成年女性在童年时遭受创伤性脑损伤,导致脑半球萎缩,但功能缺陷极小。本研究还总结了现有数据,并讨论了神经可塑性和脑网络连通性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e27/12005121/f18fa75b0820/cureus-0017-00000080762-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e27/12005121/0f799b12f98b/cureus-0017-00000080762-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e27/12005121/c51e85999945/cureus-0017-00000080762-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e27/12005121/f18fa75b0820/cureus-0017-00000080762-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e27/12005121/0f799b12f98b/cureus-0017-00000080762-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e27/12005121/c51e85999945/cureus-0017-00000080762-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e27/12005121/f18fa75b0820/cureus-0017-00000080762-i03.jpg

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1
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本文引用的文献

1
Dyke-Davidoff-Masson syndrome: A rare case of hemiatrophy with chronic seizure disorder.戴克-戴维多夫-马森综合征:一例罕见的伴有慢性癫痫障碍的偏侧萎缩病例。
Radiol Case Rep. 2024 Dec 21;20(3):1470-1474. doi: 10.1016/j.radcr.2024.11.060. eCollection 2025 Mar.
2
Presentation of Dyke-Davidoff-Masson Syndrome in adult male.男性成人中 Dyke-Davidoff-Masson 综合征的表现。
Neurosciences (Riyadh). 2023 Apr;28(2):143-147. doi: 10.17712/nsj.2023.2.20220084.
3
Dyke-Davidoff-Masson Syndrome: A Case Report.戴克-戴维多夫-马森综合征:一例报告
Cureus. 2023 Feb 11;15(2):e34868. doi: 10.7759/cureus.34868. eCollection 2023 Feb.
4
A Case Report on Dyke-Davidoff-Masson Syndrome: A Rare Cause of Hemiparesis.戴克-戴维多夫-马森综合征病例报告:偏瘫的罕见病因
Cureus. 2023 Feb 4;15(2):e34637. doi: 10.7759/cureus.34637. eCollection 2023 Feb.
5
An unusual case of Dyke-Davidoff-Masson syndrome revealed by status epilepticus in a Malian patient.一名马里患者因癫痫持续状态而发现的一例罕见的戴克-戴维多夫-马森综合征病例。
Clin Case Rep. 2022 Oct 17;10(10):e6428. doi: 10.1002/ccr3.6428. eCollection 2022 Oct.
6
Dyke-Davidoff-Masson syndrome: Imaging diagnosis in an asymptomatic adult.戴克-戴维多夫-马森综合征:一名无症状成年人的影像学诊断
Radiol Case Rep. 2022 Sep 15;17(11):4328-4331. doi: 10.1016/j.radcr.2022.08.060. eCollection 2022 Nov.
7
Dyke-Davidoff-Masson syndrome: A rare case of hemiatrophy of brain-Case report from Nepal.戴克-戴维多夫-马森综合征:一例罕见的大脑半侧萎缩病例报告——来自尼泊尔的病例报告
Radiol Case Rep. 2022 Aug 10;17(10):3882-3885. doi: 10.1016/j.radcr.2022.07.057. eCollection 2022 Oct.
8
Case Report and Literature Review: COVID-19 and status epilepticus in Dyke-Davidoff-Masson syndrome.病例报告与文献综述:戴克-戴维多夫-马森综合征中的新型冠状病毒肺炎与癫痫持续状态
F1000Res. 2021 Jan 8;10:9. doi: 10.12688/f1000research.27971.1. eCollection 2021.
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Dyke-Davidoff-Masson syndrome: A case report with a literature review.戴克-戴维多夫-马森综合征:一例病例报告并文献复习
Radiol Case Rep. 2022 May 28;17(8):2616-2618. doi: 10.1016/j.radcr.2022.04.047. eCollection 2022 Aug.
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An Adult With Dyke-Davidoff-Masson Syndrome: A Case Report.一名患有戴克-戴维多夫-马森综合征的成年人:病例报告。
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