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一名患有硬脑膜动静脉分流的婴儿新发三处海绵状血管瘤。病例报告。

De Novo Appearance of Three Cavernomas in an Infant with Dural AV Shunts. Case Report.

作者信息

Janz C, Meisel J, Brock M, Lasjaunias P

机构信息

Neurochirurgische Klinik, Klinikum Benjamin Franklin, Free University of Berlin; Berlin, Germany.

出版信息

Interv Neuroradiol. 1998 Mar 30;4(1):85-90. doi: 10.1177/159101999800400111. Epub 2001 May 15.

Abstract

Cavernomas of the brain and spinal cord are malformations which are generally considered congenital and often found in young adults. Although the distinction of a sporadic and a hereditary type is discussed, the natural history is still poorly understood. We present the unusual case of an infant first submitted to CT scan, MRI and MR-angiography at the age of three months, revealing multiple AV shunts of the superior sagittal and the sigmoid sinus, with a small pial supply. A second angiogram at the age of six months showed an additional parietal pial AVM. At this time, partial embolisation of the dural AV shunts was performed. At the age of three, the child was restudied by MRI and three formerly invisible cavernomas were detected.

摘要

脑和脊髓海绵状血管瘤是一种通常被认为是先天性的畸形,常见于年轻人。虽然有关于散发性和遗传性类型的区分的讨论,但对其自然病史仍知之甚少。我们报告了一例不寻常的病例,一名婴儿在三个月大时首次接受CT扫描、MRI和磁共振血管造影检查,结果显示上矢状窦和乙状窦存在多个动静脉分流,有少量软膜供血。六个月大时的第二次血管造影显示额外的顶叶软膜动静脉畸形。此时,对硬脑膜动静脉分流进行了部分栓塞。三岁时,对该儿童再次进行MRI检查,发现了三个之前未发现的海绵状血管瘤。

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