Olivé M, Ferrer I, Arbizu T, Calopa M, Ferrer X, Peres J
Servicio de Neurología, Hospital de Bellvitge-Prínceps d'Espanya, Barcelona.
Neurologia. 1992 May;7(5):117-9.
Three patients who had had epilepsy since the second decade of life were studied with cranial magnetic resonance (MR). Two patients had no antecedents of interest during pregnancy and the perinatal period and neurological examination was normal. The third patient had had dystocia and presented left hemiparesia since then, with normal intellectual development. None of the cases had any family history of neurological disease. Cranial magnetic resonance was performed in the three patients demonstrating polymicrogyria in two and ulegyria in the other, in addition to other lesions. The first patient presented an unilateral area of polymicrogyria related with a porencephalic cyst in the distal territory of the right sylvian artery and ipsilateral heterotopia of periventricular location. The second patient presented bilateral periventricular heterotopia, partial agenesis of the corpus callosum and an enlarged cisterna magna in addition to bilateral frontal-occipital polymicrogyria. Finally, ulegyria was observed in the third patient in the edges and neighboring regions of a right rolandic porencephalic cyst, as well as an enlarged cisterna magna.
对三名自二十岁起就患有癫痫的患者进行了头颅磁共振成像(MR)检查。两名患者在孕期及围产期无相关异常情况,神经学检查正常。第三名患者曾有难产史,自那时起出现左侧偏瘫,智力发育正常。所有病例均无神经疾病家族史。对这三名患者进行了头颅磁共振成像检查,结果显示两名患者有多小脑回畸形,另一名患者有脑回发育不全,此外还有其他病变。第一名患者在右侧大脑中动脉远端区域出现与脑穿通性囊肿相关的单侧多小脑回畸形区域以及同侧脑室周围异位。第二名患者除双侧额枕叶多小脑回畸形外,还出现双侧脑室周围异位、胼胝体部分发育不全及枕大池扩大。最后,在第三名患者右侧中央区脑穿通性囊肿边缘及邻近区域观察到脑回发育不全,同时枕大池也扩大。