Felderhoff-Mueser U, Rutherford M A, Squier W V, Cox P, Maalouf E F, Counsell S J, Bydder G M, Edwards A D
Department of Pediatrics, Imperial College School of Medicine, Hammersmith Hospital, London, UK.
AJNR Am J Neuroradiol. 1999 Aug;20(7):1349-57.
MR imaging can now be used safely in extremely preterm infants. The aim of this study was to compare the MR imaging appearance of the immature brain with neuropathologic findings at postmortem examination.
Seven extremely sick preterm infants, born at a median of 24 weeks' gestation, were studied using T1- and T2-weighted MR sequences. Infants died at a median of 3 days after initial MR imaging, and postmortem examinations were carried out.
The cortex and germinal matrix were seen as areas of low signal intensity on T2-weighted images, which corresponded to their highly cellular histologic appearance. The periventricular and subcortical layers of white matter had a high signal intensity, corresponding to high fiber and relatively low cellular density; the intermediate layer of low signal intensity corresponded to a dense band of migrating cells. Regions of acute hemorrhage were seen as low signal intensity and regions of infarction as high signal intensity on T2-weighted images. One infant with mild periventricular leukomalacia had some low signal intensity on T1-weighted images, but no focal changes on T2-weighted images. Regions of neuronal mineralization, seen in association with infarction and capillary proliferation, within the basal ganglia and thalami were characterized by very low signal intensity on T2-weighted images and by very high signal intensity on T1-weighted images. There were no imaging abnormalities detected in regions with more subtle histologic abnormalities, such as increased glial or apoptotic cells.
MR imaging can be used to observe normal developing brain anatomy in extremely premature infants; it can detect areas of hemorrhage and infarction within the developing brain, but conventional MR imaging may not detect more subtle histologic abnormalities.
磁共振成像(MR成像)现在可以安全地用于极早产儿。本研究的目的是比较未成熟脑的MR成像表现与尸检时的神经病理学发现。
对7例病情极重的早产儿进行研究,这些婴儿的中位胎龄为24周,采用T1加权和T2加权MR序列进行检查。婴儿在首次MR成像后中位3天死亡,并进行了尸检。
在T2加权图像上,皮质和生发基质表现为低信号强度区域,这与它们细胞高度密集的组织学表现相对应。脑室周围和皮质下白质层呈高信号强度,对应于高纤维和相对低的细胞密度;低信号强度的中间层对应于密集的迁移细胞带。在T2加权图像上,急性出血区域表现为低信号强度,梗死区域表现为高信号强度。1例患有轻度脑室周围白质软化的婴儿在T1加权图像上有一些低信号强度,但在T2加权图像上无局灶性改变。在基底节和丘脑内,与梗死和毛细血管增生相关的神经元矿化区域在T2加权图像上表现为极低信号强度,在T1加权图像上表现为极高信号强度。在有更细微组织学异常(如胶质细胞增多或凋亡细胞增多)的区域未检测到成像异常。
MR成像可用于观察极早产儿正常发育的脑解剖结构;它可以检测发育中脑内的出血和梗死区域,但传统的MR成像可能无法检测到更细微的组织学异常。