Ferrer I, Catalá I
Departamento Anatomía Patológica, Hospital Príncipes de España, Facultad de Medicina, Universidad de Barcelona, Spain.
Anat Embryol (Berl). 1991;184(5):517-28. doi: 10.1007/BF01236058.
Unlayered polymicrogyria was analyzed in four patients with established lesions and in one 19- to 20-week-old fetus with lesions in a formative stage whose mother had suffered a serious accident two weeks before. Polymicrogyria occurred at the banks of porencephalic, sylvian clefts in three cases, and bilaterally in the watershed areas of the parieto-occipital lobes in a fourth case. Periventricular neuronal heteropias were found in these cases. Cortical lesions in the fetus were distributed along the watershed zones of the middle cerebral artery. Serial sections revealed that the appearance of microgyria was the result of radial tissue cleavage of the cerebral cortex, as shown by the increased numbers of blood vessels and astrocytes forming a tissue scar. Golgi studies disclosed that the different neuronal types were positioned at the apropriate cortical depths in the microgyric cortex. On the other hand, heterotopic nodules were composed of pyramidal and non-pyramidal neurons usually found in the upper cortical layers in the normal cortex. These features indicate that unlayered polymicrogyria is produced by circulatory failure occurring before the end of the period of neuroblast migration to the cortical plate. Circulatory failure in the radial and unbranched arteries that penetrate from the meningeal surface and vascularize the cerebral cortex at midgestation may result in radial tissue necrosis of the cortical mantle, whereas failure in the distal, terminal territories of these blood vessels may damage radial glial fibres and impair the last migration of neuroblasts. The particular morphology of this cortical abnormality finally depends on the imbalance in the tangential growth of adjoining cortical areas variably destroyed by tissue necrosis.
对4例已确诊病变的患者以及1例19至20周龄处于病变形成阶段的胎儿进行了分析,该胎儿的母亲在两周前遭遇了严重事故。在3例中,多小脑回出现在脑穿通畸形、大脑外侧裂的边缘,在第4例中,双侧出现在顶枕叶的分水岭区域。在这些病例中发现了脑室周围神经元异位。胎儿的皮质病变沿大脑中动脉的分水岭区分布。连续切片显示,小脑回的出现是大脑皮质放射状组织裂开的结果,这表现为形成组织瘢痕的血管和星形胶质细胞数量增加。高尔基染色研究表明,不同类型的神经元位于微脑回皮质的适当皮质深度。另一方面,异位结节由通常在正常皮质上层发现的锥体细胞和非锥体细胞组成。这些特征表明,非层状多小脑回是由神经母细胞迁移至皮质板结束前发生的循环衰竭所致。在妊娠中期从脑膜表面穿透并为大脑皮质供血的放射状无分支动脉的循环衰竭,可能导致皮质被膜的放射状组织坏死,而这些血管远端终末区域的衰竭可能会损害放射状胶质纤维并影响神经母细胞的最后迁移。这种皮质异常的特殊形态最终取决于相邻皮质区域因组织坏死而受到不同程度破坏后,其切线生长的不平衡。