Lazea Cecilia, Al-Khzouz Camelia, Sufana Crina, Miclea Diana, Asavoaie Carmen, Filimon Ioana, Fufezan Otilia
Department Mother and Child, University of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.
Department of Pediatrics I, Emergency Pediatric Hospital, Cluj-Napoca, Romania.
Ther Clin Risk Manag. 2022 Mar 16;18:233-248. doi: 10.2147/TCRM.S348366. eCollection 2022.
Middle aortic syndrome (MAS) is a rare vascular disease representing an important cause of severe hypertension in children. MAS is characterized by segmental or diffuse narrowing of the abdominal and/or distal descending aorta with involvement of the renal and visceral branches. Most cases of MAS are idiopathic, but MAS may occur in genetic and acquired disorders. The most common genetic causes of MAS are neurofibromatosis type I, Williams syndrome, Alagille syndrome, tuberous sclerosis and mucopolysaccharidosis. This review article discusses the pathophysiological aspects, distinctive associated features, and management of genetic forms of MAS in children.
中段主动脉综合征(MAS)是一种罕见的血管疾病,是儿童严重高血压的重要病因。MAS的特征是腹主动脉和/或降主动脉远端节段性或弥漫性狭窄,并累及肾动脉和内脏分支。大多数MAS病例为特发性,但也可能发生于遗传性和获得性疾病。MAS最常见的遗传病因是I型神经纤维瘤病、威廉姆斯综合征、阿拉吉尔综合征、结节性硬化症和黏多糖贮积症。这篇综述文章讨论了儿童MAS遗传形式的病理生理学方面、独特的相关特征及治疗。