Hanna Ramy Magdy, Yang Wan-Ting, Jene Kim Susan, Lopez Eduardo A, Riad Joseph Nabil, Wilson James
Department of Medicine, Olive-View UCLA Medical Center, Los Angeles, CA 91342, USA ; The David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA ; Division of Nephrology, Olive-View UCLA Medical Center, Los Angeles, CA 91342, USA.
Case Rep Med. 2012;2012:839795. doi: 10.1155/2012/839795. Epub 2012 Nov 28.
Takayasu's arteritis (TA) is a medium and large vessel vasculitis, defined as a nonspecific aortitis that usually involves the aorta and its branches Kobayashi and Numano (2002). Its etiology remains unclear, and its complications are diverse and severe, including stenosis of the thoracic and abdominal aorta, aortic valve damage and regurgitation, and stenosis of the branches of the aorta. Carotid stenosis, coronary artery aneurysms, and renal artery stenosis resulting in renovascular hypertension are also reported sequellae of TA Kobayashi and Numano (2002). The disease was first described in Japan, but has also been diagnosed in India and Mexico Johnston (2002). Its incidence in the United States has been quoted as 2.6 patients per 1,000,000 people/year Johnston (2002). In Japan, its incidence is 3.6 patients per 1,000,000 patients/year and prevalence is 7.85 patients per 100,000 per year Morita et al. (1996). The natural history of this disease, which is commonly present in Asian populations, has only recently been studied in Hispanic patients despite the notable incidence and prevalence of TA in Mexican, South American, and Indian populations (Johnston 2002, Gamarra et al. 2010 ). We present three cases of Hispanic patients who presented with TA at Olive-View-UCLA Medical Center (OVMC). We review their clinical and radiographic presentations. Finally, we review the literature to compare the clinical features of our three patients with data regarding the presentation of TA in more traditional Asian populations.
高安动脉炎(TA)是一种中大型血管炎,被定义为一种通常累及主动脉及其分支的非特异性主动脉炎(小林和沼野,2002年)。其病因仍不清楚,并发症多样且严重,包括胸主动脉和腹主动脉狭窄、主动脉瓣损害和反流,以及主动脉分支狭窄。颈动脉狭窄、冠状动脉瘤和导致肾血管性高血压的肾动脉狭窄也被报道为TA的后遗症(小林和沼野,2002年)。该疾病最初在日本被描述,但在印度和墨西哥也有诊断报道(约翰斯顿,2002年)。据报道,其在美国的发病率为每100万人每年2.6例(约翰斯顿,2002年)。在日本,其发病率为每100万人每年3.6例,患病率为每年每10万人7.85例(森田等人,1996年)。尽管TA在墨西哥、南美和印度人群中的发病率和患病率显著,但这种常见于亚洲人群的疾病的自然史直到最近才在西班牙裔患者中得到研究(约翰斯顿,2002年;加马拉等人,2010年)。我们介绍了三例在奥利夫-维尤-加州大学洛杉矶分校医学中心(OVMC)就诊的患有TA的西班牙裔患者。我们回顾了他们的临床和影像学表现。最后,我们查阅文献,将我们三名患者的临床特征与关于更传统亚洲人群中TA表现的数据进行比较。