Abstract

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.

Highlights

  • 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 Takayasu’s arteritis (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)

  • Takayasu’s arteritis (TA) is a rare condition characterized by idiopathic chronic inflammation of the medium and large vessels

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Summary

Introduction

Takayasu’s arteritis (TA) is a rare condition characterized by idiopathic chronic inflammation of the medium and large vessels It often affects the aorta and its major branches. Extensive research in Central America did bring to light a causative association not common in Japanese populations of TA patients. This is the newly documented link between Mycobacterium Tuberculosis infection and TA [5, 8]. New links between ulcerative colitis (UC) and TA have come to light in case reports of Turkish and Japanese patients [9,10,11] It remains to be seen whether these associations will be found in the HispanicAmerican population. The three cases are described in detail below along with pertinent clinical and radiographical findings

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