De novo appearance of three cavernomas in an infant with dural AV shunts - Case report

被引:6
作者
Janz, C [1 ]
Meisel, J
Brock, M
Lasjaunias, P
机构
[1] Free Univ Berlin, Klinikum Benjamin Franklin, Neurochirurg Klin, D-1000 Berlin, Germany
[2] Univ Paris Sud, Hop Bicetre, Paris, France
来源
INTERVENTIONAL NEURORADIOLOGY | 1998年 / 4卷 / 01期
关键词
dural AV shunts; cavernoma; children;
D O I
10.1177/159101999800400111
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:85 / 90
页数:6
相关论文
共 5 条
[1]  
GALLINA P, 1994, NEUROCHIRURGIE, V40, P322
[2]   A founder mutation as a cause of cerebral cavernous malformation in Hispanic Americans [J].
Gunel, M ;
Awad, IA ;
Finberg, K ;
Anson, JA ;
Steinberg, GR ;
Batjer, PH ;
Kopitnik, TA ;
Morrison, L ;
Giannotta, SL ;
NelsonWilliams, C ;
Lifton, RP .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (15) :946-951
[3]  
HOROWITZ M, 1995, AM J NEURORADIOL, V16, P1353
[4]   FAMILIAL CEREBRAL CAVERNOUS ANGIOMAS - CLINICAL AND RADIOLOGIC STUDIES [J].
KATTAPONG, VJ ;
HART, BL ;
DAVIS, LE .
NEUROLOGY, 1995, 45 (03) :492-497
[5]  
LASJAUNIAS P, 1997, VASCULAR DIS NEONATE, P51