Clatterbuck R E, Elmaci I, Rigamonti D
Department of Neurosurgery, The Johns Hopkins Hospital, Baltimore, Maryland 21287, USA.
Neurosurgery. 2001 Jul;49(1):26-30; discussion 30-2. doi: 10.1097/00006123-200107000-00004.
Four types of cavernous malformations (Types I-IV) have been described on the basis of their magnetic resonance imaging (MRI) appearance. The nature of the Type IV cavernous malformation is unclear. It has been suggested that these small lesions, which are well observed only on gradient echo MRI scans, are capillary telangiectasias. We sought to understand the relationship of Type IV cavernous malformations to the other cavernous malformation subtypes.
We examined serial MRI scans obtained between 1987 and 2000 from 68 patients with more than 228 cavernous malformations. Sixteen patients harbored Type IV cavernous malformations (total, >114 Type IV lesions). Spin echo T1-weighted, T2-weighted, proton density, and (when available) gradient echo MRI scans were reviewed. Cavernous malformations that met the Zabramski criteria for Type IV (poorly observed on T1- and T2-weighted images) were reviewed in serial scans from individual patients to characterize their radiographic behavior over time.
Type IV cavernous malformations were best observed on gradient echo images and have an MRI appearance distinct from capillary telangiectasias. Proton density images demonstrate more Type IV lesions than T1- and T2-weighted images, but far fewer Type IV lesions than gradient echo images. When observed on T1- and T2-weighted images, Type IV cavernous malformations are generally punctate and hypointense. These lesions rarely enhance with gadolinium. Four of the Type IV cavernous malformations observed serially evolved into Type I and Type II cavernous malformations, for an approximate rate of progression of 0.05 per patient year.
Although most Type IV cavernous malformations remain stable over time, a small subset of these lesions progress into Types I and II cavernous malformations.
根据磁共振成像(MRI)表现,已描述了四种类型的海绵状血管畸形(I - IV型)。IV型海绵状血管畸形的性质尚不清楚。有人提出,这些仅在梯度回波MRI扫描上才能良好观察到的小病变是毛细血管扩张症。我们试图了解IV型海绵状血管畸形与其他海绵状血管畸形亚型之间的关系。
我们检查了1987年至2000年间从68例患有228个以上海绵状血管畸形的患者中获得的系列MRI扫描。16例患者患有IV型海绵状血管畸形(总计>114个IV型病变)。回顾了自旋回波T1加权、T2加权、质子密度以及(如有)梯度回波MRI扫描。对符合Zabramski IV型标准(在T1和T2加权图像上观察不佳)的海绵状血管畸形进行了个体患者的系列扫描,以表征其随时间的影像学表现。
IV型海绵状血管畸形在梯度回波图像上观察最佳,其MRI表现与毛细血管扩张症不同。质子密度图像显示的IV型病变比T1和T2加权图像更多,但比梯度回波图像少得多。当在T1和T2加权图像上观察时,IV型海绵状血管畸形通常为点状且低信号。这些病变很少用钆增强。连续观察到的4个IV型海绵状血管畸形演变成了I型和II型海绵状血管畸形,每位患者每年的进展率约为0.05。
尽管大多数IV型海绵状血管畸形随时间保持稳定,但这些病变中的一小部分会进展为I型和II型海绵状血管畸形。