Kolberg T
Neurochirurgia (Stuttg). 1978 Jan;21(1):14-20. doi: 10.1055/s-0028-1090317.
Clinical, radiological and pathomorphological investigations on five cases offering the patterns of the so-called temporal lobe agenesis syndrome (Robinson) have shown that this is not always originally malformative, but may be due to vascular processes in the sense of porencephalic defects, with all their pathomorphological features. We think that compression of the vein of Rosenthal by inscisural hippocampal herniation is the most probable aetiological mechanism. Earle, Baldwin and Penfield also described large temporal defects in connexion with their impressive demonstration of the inscisural herniation of the hippocampal gyrus at birth. We propose to use the name of--inscisural porencephaly--for this state.
对5例呈现所谓颞叶发育不全综合征（罗宾逊综合征）模式的病例进行的临床、放射学和病理形态学研究表明，这并非总是原发性畸形，而是可能由于脑穿通畸形缺损意义上的血管病变所致，具有其所有的病理形态学特征。我们认为，经天幕海马疝对罗森塔尔静脉的压迫是最可能的病因机制。厄尔、鲍德温和彭菲尔德在出生时对海马回经天幕疝进行了令人印象深刻的展示，他们也描述了相关的巨大颞叶缺损。我们建议将这种状态命名为——经天幕脑穿通畸形。
