Kadoya C, Momota Y, Ikegami Y, Urasaki E, Wada S, Yokota A
Department of Neurosurgery, School of Medicine, University of Occupational and Environmental Health, Japan.
Surg Neurol. 1994 Sep;42(3):234-9. doi: 10.1016/0090-3019(94)90269-0.
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.
报道了一个患有中枢神经系统(CNS)动静脉畸形(AVM)和遗传性出血性毛细血管扩张症(HHT)的家族。一名46岁男性发生脑出血。脑血管造影显示一处AVM和两处血管瘤。由于同时存在皮肤毛细血管扩张症,故诊断为HHT。患者的兄弟自21岁起患有HHT和截瘫。磁共振成像显示陈旧性脊髓出血。患者患有HHT的儿子在6岁时发生脑出血。血管造影显示两处AVM和一处血管瘤。伴有HHT的家族性CNS AVM极为罕见。对患有HHT的受累病例的人类白细胞抗原位点进行了评估,并讨论了伴有HHT的CNS AVM的治疗。