Pasqualin A, Mazza C, Da Pian R, Dala Bernardina B
Acta Neurochir (Wien). 1982;64(3-4):259-71. doi: 10.1007/BF01406061.
Three rare cases of giant midline arterio-venous malformations are presented. The first case is an infant girl with a vein of Galen malformation, who died from a subarachnoid haemorrhage a few weeks after shunt insertion for the control of hydrocephalus. The second case is an infant girl with a massive dilatation of the superior longitudinal sinus, who died from acute cardiac decompensation following direct surgery on the malformation. The third case is an infant boy with very large bilateral angiomas of the basal ganglia, who was not treated surgically. Some unusual features of these cases are discussed. Anatomically, the lesion can be quite different from a typical vein of Galen malformation. Clinically, the presence of cardiac failure and hydrocephalus is not always the case, and the possibility of a subarachnoid haemorrhage must be considered. For these reasons, infants with giant midline AVMs should be treated individually, balancing various considerations.
本文报告了三例罕见的巨大中线动静脉畸形病例。第一例是一名患有大脑大静脉畸形的女婴,在插入分流管以控制脑积水几周后死于蛛网膜下腔出血。第二例是一名患有上矢状窦巨大扩张的女婴,在对畸形进行直接手术后死于急性心功能不全。第三例是一名患有基底节区非常大的双侧血管瘤的男婴,未接受手术治疗。讨论了这些病例的一些不寻常特征。从解剖学角度来看,病变可能与典型的大脑大静脉畸形有很大不同。在临床上,并不总是出现心力衰竭和脑积水的情况,必须考虑蛛网膜下腔出血的可能性。由于这些原因,患有巨大中线动静脉畸形的婴儿应根据各种因素进行个体化治疗。