Suppr超能文献

类岛带征:一种与聚合酶γ相关疾病相关的独特影像学发现。

The Perirolandic Sign: A Unique Imaging Finding Observed in Association with Polymerase γ-Related Disorders.

机构信息

From the Departments of Radiology and Division of Neuroradiology (F.G.G., B.H., C.A.P.F.A., S.R.T., J.S.M.-S., A.V., G.Z.)

From the Departments of Radiology and Division of Neuroradiology (F.G.G., B.H., C.A.P.F.A., S.R.T., J.S.M.-S., A.V., G.Z.).

出版信息

AJNR Am J Neuroradiol. 2020 May;41(5):917-922. doi: 10.3174/ajnr.A6514. Epub 2020 May 7.

Abstract

Pathogenic variants in the () cause a diverse group of pathologies known as -related disorders. In this report, we describe brain MR imaging findings and electroencephalogram correlates of 13 children with -related disorders at diagnosis and follow-up. At diagnosis, all patients had seizures and 12 had abnormal MR imaging findings. The most common imaging findings were unilateral or bilateral perirolandic (54%) and unilateral or bilateral thalamic signal changes (77%). Association of epilepsia partialis continua with perirolandic and thalamic signal changes was present in 86% and 70% of the patients, respectively. The occipital lobe was affected in 2 patients. On follow-up, 92% of the patients had disease progression or fatal outcome. Rapid volume loss was seen in 77% of the patients. The occipital lobe (61%) and thalamus (61%) were the most affected brain regions. Perirolandic signal changes and seizures may represent a brain imaging biomarker of early-onset pediatric -related disorders.

摘要

致病变异位于 () 会导致一组不同的病理学表现,被称为 - 相关障碍。在本报告中,我们描述了 13 名 - 相关障碍患儿在诊断和随访时的脑部磁共振成像 (MRI) 表现和脑电图相关性。在诊断时,所有患者都有癫痫发作,12 名患者有异常的 MRI 发现。最常见的影像学表现为单侧或双侧旁中央区(54%)和单侧或双侧丘脑信号改变(77%)。癫痫部分持续状态与旁中央区和丘脑信号改变的关联分别见于 86%和 70%的患者。2 名患者的枕叶受累。随访时,92%的患者疾病进展或出现致死性结局。77%的患者出现快速体积丢失。枕叶(61%)和丘脑(61%)是最受影响的脑区。旁中央区信号改变和癫痫发作可能是儿童期 - 相关障碍的早期脑影像学生物标志物。

相似文献

1
The Perirolandic Sign: A Unique Imaging Finding Observed in Association with Polymerase γ-Related Disorders.
AJNR Am J Neuroradiol. 2020 May;41(5):917-922. doi: 10.3174/ajnr.A6514. Epub 2020 May 7.
2
Diagnostic algorithm for children presenting with epilepsia partialis continua.
Epilepsia. 2020 Oct;61(10):2224-2233. doi: 10.1111/epi.16650. Epub 2020 Sep 2.
3
Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from India.
J Mol Neurosci. 2021 Nov;71(11):2219-2228. doi: 10.1007/s12031-020-01765-8. Epub 2021 Jan 19.
5
The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations.
Genet Med. 2017 Nov;19(11):1217-1225. doi: 10.1038/gim.2017.35. Epub 2017 Apr 27.
6
Decreased Subcortical T2 FLAIR Signal Associated with Seizures.
AJNR Am J Neuroradiol. 2020 Jan;41(1):111-114. doi: 10.3174/ajnr.A6328. Epub 2019 Dec 5.
7
[Clinical and genetic characteristics of 62 children with mitochondrial epilepsy].
Zhonghua Er Ke Za Zhi. 2019 Nov 2;57(11):844-851. doi: 10.3760/cma.j.issn.0578-1310.2019.11.006.
8
Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review.
Epilepsia. 2016 Oct;57(10):1531-1545. doi: 10.1111/epi.13508. Epub 2016 Aug 24.
10
Status epilepticus in POLG disease: a large multinational study.
J Neurol. 2024 Aug;271(8):5156-5164. doi: 10.1007/s00415-024-12463-5. Epub 2024 Jun 1.

引用本文的文献

1
Spectrum of clinical neuroimaging in mitochondrial disorders: a neuroanatomical approach.
Pediatr Radiol. 2025 May 2. doi: 10.1007/s00247-025-06252-z.
2
Overview of neuroimaging in primary mitochondrial disorders.
Pediatr Radiol. 2025 Apr;55(4):765-791. doi: 10.1007/s00247-025-06172-y. Epub 2025 Feb 12.
3
Mimickers of hypoxic-ischaemic brain injury in term neonates: What the radiologist should know.
SA J Radiol. 2024 Feb 29;28(1):2810. doi: 10.4102/sajr.v28i1.2810. eCollection 2024.
4
Advancing the neuroimaging diagnosis and understanding of mitochondrial disorders.
Neurotherapeutics. 2024 Jan;21(1):e00324. doi: 10.1016/j.neurot.2024.e00324. Epub 2024 Feb 1.
5
Perirolandic Sign and Crossed Cerebellar Diaschisis in POLG-Related Disorder.
Ann Indian Acad Neurol. 2022 Sep-Oct;25(5):933-934. doi: 10.4103/aian.aian_478_22. Epub 2022 Jul 26.
6
MR Neuroimaging in Pediatric Inborn Errors of Metabolism.
Diagnostics (Basel). 2022 Mar 30;12(4):861. doi: 10.3390/diagnostics12040861.

本文引用的文献

1
Neuroimaging of acute and chronic unilateral and bilateral thalamic lesions.
Insights Imaging. 2019 Feb 22;10(1):24. doi: 10.1186/s13244-019-0700-3.
2
POLG-related disorders and their neurological manifestations.
Nat Rev Neurol. 2019 Jan;15(1):40-52. doi: 10.1038/s41582-018-0101-0.
3
Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease.
J Inherit Metab Dis. 2018 Nov;41(6):1275-1283. doi: 10.1007/s10545-018-0227-7. Epub 2018 Aug 30.
4
Imaging in Maple Syrup Urine Disease.
Indian J Pediatr. 2018 Oct;85(10):927-928. doi: 10.1007/s12098-018-2696-y. Epub 2018 May 9.
5
Alpers-Huttenlocher Syndrome First Presented with Hepatic Failure: Can Liver Transplantation Be Considered as Treatment Option?
Pediatr Gastroenterol Hepatol Nutr. 2017 Dec;20(4):259-262. doi: 10.5223/pghn.2017.20.4.259. Epub 2017 Dec 22.
6
Resection of primary motor cortex tumors: feasibility and surgical outcomes.
J Neurosurg. 2018 Oct;129(4):961-972. doi: 10.3171/2017.5.JNS163045. Epub 2017 Dec 8.
7
Teaching Video Neuro: Epilepsia partialis continua in an adolescent with preexisting focal epilepsy.
Neurology. 2017 Dec 5;89(23):e274-e275. doi: 10.1212/WNL.0000000000004713.
8
Understanding the Epilepsy in POLG Related Disease.
Int J Mol Sci. 2017 Aug 24;18(9):1845. doi: 10.3390/ijms18091845.
9
Pathogenicity in POLG syndromes: DNA polymerase gamma pathogenicity prediction server and database.
BBA Clin. 2017 Apr 18;7:147-156. doi: 10.1016/j.bbacli.2017.04.001. eCollection 2017 Jun.
10
Epilepsia partialis continua: A review.
Seizure. 2017 Jan;44:74-80. doi: 10.1016/j.seizure.2016.10.010. Epub 2016 Oct 18.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验