Jacques S, Garner J T, Shelden H, Johnson P E, Johnson D
Clin Pediatr (Phila). 1975 Nov;14(11):1031-6. doi: 10.1177/000992287501401109.
Numerous bleeding episodes, neurological signs and symptoms, and pulmonary arteriovenous malformations are well documented in reports of families with hereditary hemorrhagic telangiectasia. It is always assumed that these are due to the arteriovenous malformations. We are here reporting a case with positive cerebral angiographic findings of large arteriovenous communications, as well as catheterization data revealing pulmonary abnormalities secondary to the cerebral arteriovenous fistula, but no abnormalities within the pulmonary vasculature itself.
在遗传性出血性毛细血管扩张症家族报告中,大量出血事件、神经体征和症状以及肺动静脉畸形都有充分记录。人们一直认为这些是由动静脉畸形引起的。我们在此报告一例病例,脑血管造影显示存在大的动静脉交通,导管检查数据显示继发于脑动静脉瘘的肺部异常,但肺血管本身未见异常。