Mettinger K L
Stroke. 1982 Jan-Feb;13(1):53-8. doi: 10.1161/01.str.13.1.53.
Eleven hundred cases from the literature of fibromuscular dysplasia (FMD) are reviewed including 300 cases with aortocranial lesions. The male-female ratio is 1:2, and the prevalence seems increased among Caucasians. The clinical diagnosis of FMD is made by angiography, ten years earlier in patients with hypertension (mean age 39 years) than in those with cerebrovascular symptoms (mean age 50 years). Segmental dysplastic lesions are found mainly in primary aortic branches. All age groups may be affected and follow-up studies give evidence for stationary as well as slowly progressive lesions. A multifactorial hypothesis of etiology is presented: congenital minor lesions of tunica medial might predispose to aneurysms and to an abnormal fibroproliferative response to mechanical or circulatory stimuli. The association of FMD and intracranial aneurysmal disease in females is discussed. Inheritance as a dominant trait with reduced penetrance in males is suspected. Current aspects on morphology, symptomatology and clinical management are presented.
对文献中1100例纤维肌发育异常(FMD)病例进行了回顾,其中包括300例有主动脉-颅部病变的病例。男女比例为1:2,白种人中的患病率似乎更高。FMD的临床诊断通过血管造影做出,高血压患者(平均年龄39岁)比有脑血管症状的患者(平均年龄50岁)早十年确诊。节段性发育异常病变主要见于主动脉主要分支。所有年龄组均可受累,随访研究表明病变有静止性的,也有缓慢进展的。提出了病因的多因素假说:中膜先天性微小病变可能易患动脉瘤,并对机械或循环刺激产生异常的纤维增生反应。讨论了女性FMD与颅内动脉瘤疾病的关联。怀疑其遗传方式为显性遗传,男性的外显率降低。介绍了其形态学、症状学和临床处理的现状。