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胼胝体综合征的磁共振成像

MRI of corpus callosal syndromes.

作者信息

Curnes J T, Laster D W, Koubek T D, Moody D M, Ball M R, Witcofski R L

出版信息

AJNR Am J Neuroradiol. 1986 Jul-Aug;7(4):617-22.

PMID:3088939
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8334646/
Abstract

Six patients, 6 to 13 years old, with corpus callosal abnormalities diagnosed by electroencephalography or CT were studied with a 0.15 T MR imager to determine the effectiveness of MRI in evaluating midline anomalies. Spin-echo images in the coronal, axial, and sagittal planes were obtained in two patients with Aicardi's syndrome and partial agenesis of the corpus callosum, in one patient with Dandy-Walker syndrome, and in two patients with septooptic dysplasia. Inversion recovery and spin-echo images were obtained in one patient with lipoma of the corpus callosum. Partial agenesis of the corpus callosum was seen in septooptic dysplasia, an association that has not been reported previously in the radiologic literature. Direct sagittal and coronal MRI provided better anatomic visualization of the brain and ventricles than did reformatted CT. T1-weighted images are sufficient to diagnose and delineate the extent of midline cerebral abnormalities. The unique capability of direct sagittal imaging makes MRI the best procedure for evaluating corpus callosal and other midline abnormalities.

摘要

对6例年龄在6至13岁、经脑电图或CT诊断为胼胝体异常的患者,使用0.15T磁共振成像仪进行研究,以确定MRI在评估中线异常方面的有效性。对2例患有艾卡迪综合征和胼胝体部分发育不全的患者、1例患有丹迪-沃克综合征的患者以及2例患有视隔发育不良的患者,获取了冠状面、轴位面和矢状面的自旋回波图像。对1例患有胼胝体脂肪瘤的患者,获取了反转恢复和自旋回波图像。在视隔发育不良中发现了胼胝体部分发育不全,这种关联在放射学文献中此前尚未见报道。直接矢状面和冠状面MRI比重组CT能更好地对大脑和脑室进行解剖学可视化。T1加权图像足以诊断并描绘中线脑异常的范围。直接矢状面成像的独特能力使MRI成为评估胼胝体及其他中线异常的最佳检查方法。

相似文献

1
MRI of corpus callosal syndromes.胼胝体综合征的磁共振成像
AJNR Am J Neuroradiol. 1986 Jul-Aug;7(4):617-22.
2
Midline anomalies of the brain and spine.脑和脊柱的中线异常。
Radiol Clin North Am. 1982 Mar;20(1):95-104.
3
An atretic parietal cephalocele associated with multiple intracranial and eye anomalies.一个与多种颅内和眼部异常相关的闭锁性顶叶脑膨出。
Neuroradiology. 1998 Dec;40(12):812-5. doi: 10.1007/s002340050690.
4
Partial development of the corpus callosum.胼胝体部分发育不全。
AJNR Am J Neuroradiol. 1994 May;15(5):869-75.
5
Infantile spasms in a patient with septo-optic dysplasia, partial agenesis of the corpus callosum and an interhemispheric cyst.一名患有视隔发育不良、胼胝体部分发育不全和半球间囊肿的患者出现婴儿痉挛。
Clin Neurol Neurosurg. 1992;94(2):165-7. doi: 10.1016/0303-8467(92)90076-f.
6
Agenesis of corpus callosum: clinical description and etiology.胼胝体发育不全:临床描述与病因学
J Child Neurol. 2000 Jun;15(6):401-5. doi: 10.1177/088307380001500609.
7
Septo-optic dysplasia associated with cerebral cortical dysplasia (cortico-septo-optic dysplasia).与大脑皮质发育异常相关的视隔发育不良(皮质-视隔发育不良)。
J Neuroradiol. 1996 Dec;23(4):245-7.
8
[Magnetic resonance imaging in agenesis of the corpus callosum].[胼胝体发育不全的磁共振成像]
No To Shinkei. 1985 Dec;37(12):1203-10.
9
Absence of the septum pellucidum and related disorders.透明隔缺如及相关疾病。
Comput Med Imaging Graph. 1993 Mar-Apr;17(2):137-47. doi: 10.1016/0895-6111(93)90056-s.
10
MR imaging of pericallosal lipoma.胼胝体脂肪瘤的磁共振成像
AJNR Am J Neuroradiol. 1988 Sep;9(5):929-31.

引用本文的文献

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Brain plasticity following corpus callosum agenesis or loss: a review of the Probst bundles.胼胝体发育不全或缺失后的脑可塑性:Probst束综述
Front Neuroanat. 2023 Nov 6;17:1296779. doi: 10.3389/fnana.2023.1296779. eCollection 2023.
2
Magnetic Resonance Imaging Findings in Fetal Corpus Callosal Developmental Abnormalities: A Pictorial Essay.胎儿胼胝体发育异常的磁共振成像表现:图文综述。
J Pediatr Neurosci. 2020 Oct-Dec;15(4):352-357. doi: 10.4103/jpn.JPN_174_19. Epub 2021 Jan 19.
3
Unusual clinical history of a male infant with Edwards syndrome.一名患有爱德华兹综合征男婴的不寻常临床病史。
Pathol Oncol Res. 2009 Mar;15(1):147-52. doi: 10.1007/s12253-008-9023-2. Epub 2008 Jun 25.
4
Lesions of the corpus callosum in hydrocephalic patients with ventricular drainage--a CT-study.脑室引流脑积水患者胼胝体病变的CT研究
Acta Neurochir (Wien). 1996;138(2):174-8. doi: 10.1007/BF01411357.
5
Corpus callosum lipoma with frontal encephalocele.胼胝体脂肪瘤伴额叶脑膨出。
Neuroradiology. 1990;32(1):50-2. doi: 10.1007/BF00593942.