Barkovich A J, Kjos B O, Norman D, Edwards M S
Department of Radiology, Letterman Army Medical Center, Presidio of San Francisco, CA 94129-6700.
AJR Am J Roentgenol. 1989 Dec;153(6):1289-300. doi: 10.2214/ajr.153.6.1289.
MR and clinical data on 31 patients with posterior fossa CSF collections were analyzed. A clear separation of these patients into classical categories was not possible because of new information obtained from the MR images. We present a new classification of these disorders. The Dandy-Walker malformation, Dandy-Walker variant, and mega-cisterna magna seem to represent a continuum of developmental anomalies of the posterior fossa. A possible embryologic basis for this continuum is suggested. Discrete posterior fossa CSF collections that are clearly separate from the fourth ventricle and vallecula are classified as posterior fossa cysts. Posterior fossa CSF collections that communicate with the fourth ventricle and are associated with cerebellar atrophy are classified as prominent cisterna magna. Both the Dandy-Walker complex and posterior fossa cysts can cause enlargement of the posterior fossa and scalloping of the inner table of the occipital bone. The Dandy-Walker complex presents with seizures, developmental delay, and enlarging head size; it requires CSF diversion when associated with hydrocephalus. Posterior fossa cysts present with symptoms of a posterior fossa mass; they generally require surgical resection. Prominent cisterna magna is a result of degenerative disorders and requires no surgical therapy. This new classification facilitates both diagnosis and therapy of these disorders. MR revealed that disorders previously referred to as the Dandy-Walker malformation, the Dandy-Walker variant, and the mega-cisterna magna actually are not separate entities, but appear to represent steps on a continuum of developmental anomalies of the posterior fossa. Because of this, we suggest a new term, the Dandy-Walker complex, be used to describe this continuum.
对31例后颅窝脑脊液聚集患者的磁共振成像(MR)和临床数据进行了分析。由于从MR图像中获得了新信息,无法将这些患者明确分为经典类别。我们提出了这些疾病的一种新分类。Dandy-Walker畸形、Dandy-Walker变异型和巨大枕大池似乎代表了后颅窝发育异常的一个连续过程。提出了这一连续过程可能的胚胎学基础。与第四脑室和小脑延髓池明显分开的离散性后颅窝脑脊液聚集被归类为后颅窝囊肿。与第四脑室相通并伴有小脑萎缩的后颅窝脑脊液聚集被归类为显著枕大池。Dandy-Walker复合体和后颅窝囊肿均可导致后颅窝扩大和枕骨内板扇贝样改变。Dandy-Walker复合体表现为癫痫发作、发育迟缓及头围增大;与脑积水相关时需要进行脑脊液分流。后颅窝囊肿表现为后颅窝肿块的症状;通常需要手术切除。显著枕大池是退行性疾病的结果,无需手术治疗。这种新分类有助于这些疾病的诊断和治疗。MR显示,以前称为Dandy-Walker畸形、Dandy-Walker变异型和巨大枕大池的疾病实际上并非独立的实体,而是似乎代表了后颅窝发育异常连续过程中的不同阶段。因此,我们建议使用一个新术语“Dandy-Walker复合体”来描述这一连续过程。