A case of macrocephaly-cutis marmorata telangiectatica congenita and review of neuroradiologic features

Nevbahar Akcar , Baki Adapinar , Cagri Dinleyici , Beyhan Durak , I.Ragıp Özkan
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引用次数: 21

Abstract

Macrocephaly-cutis marmorata telangiectatica congenita (M-CMTC) is characterized by macrocephaly, cutis marmorata, capillary malformations, toe syndactily, joint laxity and pre-natal overgrowth. Cerebral abnormalities might also be seen. We reported cerebral magnetic resonance imaging (MRI) findings of a case with M-CMTC, who had giant atrial septal aneurysm and atrial septal defect. Cerebral alterations determined by MRI were bilateral prominent lateral ventricles, bilateral cortical dysplasia, cavum septi pellucidum cyst and calvarial hemangioma. At 17th day of his life he suddenly developed cardiorespiratory arrest and died.

先天性毛细血管扩张性巨头症1例及神经影像学分析
先天性巨头-皮肤毛细血管扩张症(M-CMTC)的特点是大头畸形、皮肤畸形、毛细血管畸形、脚趾并拢、关节松弛和产前过度生长。大脑异常也可能被发现。我们报告了一例伴有巨大房间隔动脉瘤和房间隔缺损的M-CMTC患者的脑磁共振成像(MRI)结果。MRI表现为双侧侧脑室突出、双侧皮质发育不良、透明中隔腔囊肿和颅骨血管瘤。在他出生的第17天,他突然出现心肺骤停并死亡。
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