Canyigit Murat, Peynircioglu Bora, Hazirolan Tuncay, Dagoglu Merve Gulbiz, Cil Barbaros Erhan, Haliloglu Mithat, Balkanci Ferhun, Besim Aytekin
Department of Radiology, Faculty of Medicine, Hacettepe University, Sihhiye, 06100, Ankara, Turkey.
Cardiovasc Intervent Radiol. 2007 Jul-Aug;30(4):711-8. doi: 10.1007/s00270-007-9050-5.
Takayasu arteritis is a rare, large-vessel vasculitis in which the nonspecific systemic inflammatory symptoms are followed by inflammation of the aorta and its major branches. The inflammation of this vessel leads to progressive luminal stenosis or aneurysm formation resulting in limb or organ ischemia. Although conventional angiography is still accepted as the gold standard modality, the information obtained is limited to the vessel lumen. Multidetector computed tomographic angiography and magnetic resonance angiography can provide valuable information not only regarding intraluminal pathologies but also concerning the thickening of the vessel wall, which may be the earliest manifestation of the disease.
高安动脉炎是一种罕见的大血管血管炎,其特征是在出现非特异性全身炎症症状后,主动脉及其主要分支发生炎症。这种血管的炎症会导致管腔逐渐狭窄或形成动脉瘤,进而导致肢体或器官缺血。尽管传统血管造影仍被视为金标准检查方式,但所获得的信息仅限于血管腔。多排螺旋计算机断层血管造影和磁共振血管造影不仅可以提供有关管腔内病变的有价值信息,还能提供有关血管壁增厚的信息,而血管壁增厚可能是该病的最早表现。