CENTRAL-NERVOUS-SYSTEM ARTERIOVENOUS-MALFORMATIONS WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA - REPORT OF A FAMILY WITH 3 CASES

被引：27

作者：

KADOYA, C

MOMOTA, Y

IKEGAMI, Y

URASAKI, E

WADA, SI

YOKOTA, A

机构：

[1] Department of Neurosurgery, School of Medicine, University of Occupational and Environmental Health

来源：

SURGICAL NEUROLOGY | 1994年 / 42卷 / 03期

关键词：

CEREBRAL ARTERIOVENOUS MALFORMATION; HEREDITARY HEMORRHAGIC TELANGIECTASIA; HUMAN LEUKOCYTE ANTIGEN (HLA); MAGNETIC RESONANCE IMAGING (MRI); RENDU-OSLER-WEBER DISEASE; SPINAL ARTERIOVENOUS MALFORMATION;

D O I：

10.1016/0090-3019(94)90269-0

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

A family with central nervous system (CNS) arteriovenous malformations (AVMs) and hereditary hemorrhagic telangiectasia (HHT) is reported. A 46-year-old man had an intracerebral hemorrhage. Cerebral angiography showed one AVM and two angiomas. The HHT was diagnosed because of the concomitant existence of cutaneous telangiectasia. The patient's brother had HHT and paraplegia since the age of 21. Magnetic resonance imaging revealed an old spinal cord hemorrhage. The patient's son with HHT had an intracerebral hemorrhage at age 6. Angiograms showed two AVMs and one angioma. Familial CNS AVMs with HHT are extremely rare. The loci for human leukocyte antigen of the affected cases with HHT were evaluated, and the management of CNS AVMs with HHT is discussed.

引用

页码：234 / 239

页数：6

共 28 条

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