Barkovich A J, Lindan C E
University of California San Francisco, Department of Radiology 94143-0628.
AJNR Am J Neuroradiol. 1994 Apr;15(4):703-15.
To analyze the cortical gyral patterns and myelination patterns in a series of patients with congenital cytomegalovirus infections involving the central nervous system, to correlate them with known developmental events, and to develop a consistent theory regarding their embryogenesis.
The MR (11 patients) and CT (four patients) studies of 11 patients with congenital cytomegalovirus infections involving the brain were retrospectively reviewed. Analysis was made of myelination patterns, cortical gyral patterns, other areas of maldeveloped brain, and focal brain lesions.
Lissencephaly was found in four patients. These patients had very thin cerebral cortices, extremely diminished volume of white matter, delayed myelination, small cerebella, and very enlarged lateral ventricles. Focal areas of dysplastic cortex, presumably polymicrogyria, were found in five patients. These patients had slightly thickened irregular cerebral cortices, slightly diminished volume of white matter, delayed myelination, variably small cerebella, and slightly enlarged lateral ventricles. Two patients had normal cerebral cortices, slightly diminished volume of white matter, delayed myelination, normal cerebella, and slightly enlarged lateral ventricles. Periventricular lesions, representing calcification, or perhaps blood, were seen in all groups.
We postulate that the patients with lissencephaly suffer injury before 16 or 18 weeks gestational age, whereas those with regions of polymicrogyria are injured between approximately 18 and 24 weeks gestational age. Those with normal gyral patterns are probably injured during the third trimester and may have active infections at birth. Moreover, we propose that the finding of cerebellar hypoplasia and myelination delay in association with diffuse lissencephaly or cortical dysplasia should suggest the diagnosis of congenital cytomegalovirus infection.
分析一系列先天性巨细胞病毒感染累及中枢神经系统患者的皮质脑回模式和髓鞘形成模式,将它们与已知的发育事件相关联,并就其胚胎发生形成一个连贯的理论。
对11例先天性巨细胞病毒感染累及脑部患者的磁共振成像(11例患者)和计算机断层扫描(4例患者)研究进行回顾性分析。分析髓鞘形成模式、皮质脑回模式、其他脑发育不良区域和局灶性脑病变。
4例患者发现无脑回畸形。这些患者的大脑皮质非常薄,白质体积极度减小,髓鞘形成延迟,小脑小,侧脑室非常扩大。5例患者发现皮质发育异常的局灶性区域,推测为多小脑回。这些患者的大脑皮质不规则增厚,白质体积略有减小,髓鞘形成延迟,小脑大小不一,侧脑室略有扩大。2例患者大脑皮质正常,白质体积略有减小,髓鞘形成延迟,小脑正常,侧脑室略有扩大。所有组均可见脑室周围病变,表现为钙化或可能为血液。
我们推测无脑回畸形患者在妊娠16或18周之前受到损伤,而多小脑回区域的患者在妊娠约18至24周之间受到损伤。脑回模式正常的患者可能在妊娠晚期受到损伤,出生时可能有活动性感染。此外,我们提出,小脑发育不全和髓鞘形成延迟与弥漫性无脑回畸形或皮质发育异常相关的发现应提示先天性巨细胞病毒感染的诊断。