Tortori-Donati P, Fondelli M P, Rossi A, Carini S
Department of Neuroradiology, Children's Hospital G. Gaslini, Genoa, Italy.
Childs Nerv Syst. 1996 Jun;12(6):303-8. doi: 10.1007/BF00301017.
Cystic malformations of the posterior cranial fossa are all but arachnoid cysts contained within the general context of the Dandy-Walker complex and may be further classified in two groups on the basis of their embryological origin: anomalies of the anterior membranous area (AMA) and anomalies of the posterior membranous area (PMA). Whether the latter group of malformations can be regarded as separate entities is still quite controversial. The present authors give a detailed account of the various embryological stages in the formation of the posterior cranial fossa and its contents and propose the identification of two anomalies derived from a defect of the PMA: the mega cisterna magna (MCM) and the persisting Blake's pouch, a new entity with different MRI features from MCM. Criteria for their recognition are discussed, stressing the capital importance of a differential diagnosis in view of the radically different therapeutic approach.
颅后窝囊性畸形几乎都是包含在Dandy-Walker综合征范畴内的蛛网膜囊肿,根据其胚胎学起源可进一步分为两组:前膜性区(AMA)异常和后膜性区(PMA)异常。后一组畸形是否可视为独立的实体仍颇具争议。本文作者详细阐述了颅后窝及其内容物形成过程中的各个胚胎学阶段,并提出识别两种源于PMA缺陷的异常:巨大枕大池(MCM)和持续存在的Blake囊袋,这是一种具有与MCM不同MRI特征的新实体。文中讨论了它们的识别标准,强调鉴于治疗方法截然不同,鉴别诊断至关重要。