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[婴儿痉挛症中的局灶性病变]

[Focal lesions in infantile spasms].

作者信息

Cusmai R, Dulac O, Diebler C

机构信息

Service de neuropédiatrie, INSERM U-29, Hôpital Saint-Vincent-de-Paul, Paris, France.

出版信息

Neurophysiol Clin. 1988 Jun;18(3):235-41. doi: 10.1016/s0987-7053(88)80028-5.

DOI:10.1016/s0987-7053(88)80028-5
PMID:3398829
Abstract

Among 174 cases of infantile spasms examined by CT-scan between January 80 and December 85, 17 (9.8%) had a focal lesion without microcephaly. It consisted of an angioma (1 case), a cortical dysplasia (1 case) and porencephalic lesions (15 cases). In 11 cases with porencephaly, an acute event had occurred between 28 weeks of gestation and 3 months of life. In 7 cases, the lesion extended to the major part of one hemisphere. In the 10 others, it was localized either to the rolandic or to the temporo-occipital regions. In all the cases, the lesion concerned at least one of these areas. It involved the cortex in 15 cases but in the 2 others it seemed to only concern the white matter. The lesion was on the left in 14 cases. After steroids, the epilepsy recurred in 6 cases of which 5 involved the frontal lobe (P less than 0.05). This study seems to show that it is mainly the rolandic and the temporo-occipital areas that favour the occurrence of infantile spasms, whereas extension to the frontal area is responsible of a later partial epilepsy.

摘要

在1980年1月至1985年12月期间接受CT扫描检查的174例婴儿痉挛症病例中,17例(9.8%)有局灶性病变但无小头畸形。病变包括1例血管瘤、1例皮质发育异常和15例脑穿通畸形。在11例脑穿通畸形病例中,在妊娠28周和出生后3个月之间发生了急性事件。7例中,病变扩展至一个半球的大部分。在其他10例中,病变局限于中央沟或颞枕区域。在所有病例中,病变至少累及这些区域之一。15例累及皮质,但另外2例似乎仅累及白质。14例病变位于左侧。使用类固醇后,6例癫痫复发,其中5例累及额叶(P<0.05)。这项研究似乎表明,主要是中央沟和颞枕区域易发生婴儿痉挛症,而扩展至额叶则导致后期的部分性癫痫。

相似文献

1
[Focal lesions in infantile spasms].[婴儿痉挛症中的局灶性病变]
Neurophysiol Clin. 1988 Jun;18(3):235-41. doi: 10.1016/s0987-7053(88)80028-5.
2
West syndrome due to perinatal insults.围产期损伤所致的韦斯特综合征
Epilepsia. 1993 Jul-Aug;34(4):738-42. doi: 10.1111/j.1528-1157.1993.tb00455.x.
3
Localization of focal cortical lesions influences age of onset of infantile spasms.
Epilepsia. 1996 Nov;37(11):1068-71. doi: 10.1111/j.1528-1157.1996.tb01026.x.
4
Infantile spasm-associated microencephaly in tuberous sclerosis complex and cortical dysplasia.结节性硬化症和皮质发育异常中与婴儿痉挛相关的小头畸形。
Neurology. 2007 Feb 6;68(6):438-45. doi: 10.1212/01.wnl.0000252952.62543.20.
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Regional specificity of localized cortical lesions in West syndrome.
Pediatr Neurol. 2000 Sep;23(3):219-24. doi: 10.1016/s0887-8994(00)00173-9.
6
Focal dysplasia of the cerebral cortex and infantile spasms associated with somatic 1q21.1-q44 duplication including the AKT3 gene.与包括AKT3基因在内的体细胞1q21.1 - q44重复相关的大脑皮质局灶性发育异常和婴儿痉挛症。
Clin Genet. 2015 Sep;88(3):241-7. doi: 10.1111/cge.12476. Epub 2014 Oct 7.
7
Infantile spasms: cerebral blood flow abnormalities correlate with EEG, neuroimaging, and pathologic findings.婴儿痉挛症:脑血流异常与脑电图、神经影像学及病理结果相关。
Pediatr Neurol. 1996 Apr;14(3):220-5. doi: 10.1016/0887-8994(96)00084-7.
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Value of magnetic resonance imaging in West syndrome of unknown etiology.磁共振成像在病因不明的韦斯特综合征中的价值。
Epilepsia. 1993 Jul-Aug;34(4):701-6. doi: 10.1111/j.1528-1157.1993.tb00449.x.
9
[MR imaging in infantile spasms].[婴儿痉挛症的磁共振成像]
No To Hattatsu. 1989 Nov;21(6):537-42.
10
[Infantile spasms with localized cerebral lesion detected by 99mTcHMPAO-SPECT].[99mTcHMPAO单光子发射计算机断层扫描检测到的伴有局限性脑病变的婴儿痉挛症]
No To Hattatsu. 1994 May;26(3):251-6.

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2
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