We encountered the rare case of a 48-year-old Caucasian woman who developed Takayasu arteritis (TA) while suffering from seropositive rheumatoid arthritis (RA). Several studies have reported an association between TA and various autoimmune disorders, however, the concurrent presence of Takayasu arteritis and rheumatoid arthritis is described in only few cases in the literature to date. The exac...

We report a case of sudden death in Takayasu arteritis after coronary artery bypass. A 22-year-old girl visited our hospital in June 2009 because of paroxysmal chest tightness and shortness of breath for 2 years. She was diagnosed as Takayasu arteritis, the limited stenosis of upper aorta ventralis, low perfusion pressure changes of double renal artery and double lower limbs artery, left ventri...

Annexin I and II were studied immunohistochemically in arteries involved by Takayasu arteritis. Results suggest that they are important in the pathophysiologic function of macrophages and endothelial cells.

Takayasu arteritis is rare in black people. Doppler echocardiography may assist in its diagnosis with good response to steroids.

A discrete stochastic process involving random amplification with additive noise is studied analytically. If the non-negative random amplification factor b is such that =1, where beta is any positive noninteger, then the steady state probability density function for the process will have power law tails of the form p(x) approximately 1/x(beta+1). This is a generalization of recent resu...

A 52-year-old woman with Takayasu arteritis developed acute coronary syndrome and received percutaneous coronary intervention (PCI). The patient experienced restenosis three times even with drug-eluting stent (DES) implantation. We started steroid administration after the fourth PCI to reduce inflammation due to autoimmunity. With DES and a steroid combination, the patient remained free of ches...

Takayasu arteritis is an inflammatory disease that affects large vessels, especially the aorta and its branches. The clinical features of the disease depend on which arteries are affected. Although pulmonary artery involvement is common, only rarely is this the main clinical manifestation. We describe the case of a young woman with dyspnea who had severe pulmonary hypertension secondary to Taka...

Takayasu arteritis is a rare, idiopathic inflammatory disease of the aorta and its major branches, usually affecting young women of Asian descent. In the course of the disease stenosis, occlusions as well as dilatations and aneurysms of vessels occur. Because of many possible localizations of pathological changes, the symptoms have a wide range, but the most common are a weak pulse or its absen...

The previously unreported CT findings of supracardiac anomalous pulmonary venous return and Takayasu arteritis are presented. CT demonstration of a left vertical vein and an enlarged superior vena cava strongly suggests a diagnosis of supracardiac anomalous venous return. Dynamic scanning of the mediastinum following bolus injection of urographic contrast with close attention to vascular enhanc...

Takayasu disease, first described by a Japanese ophthalmologist in 1908, is a chronic inflammatory arteriopathy characteristically diagnosed in young Oriental women. I It might be more common among the white population than previously appreciated, as its incidence is estimated to be 2.6 in 1,000,000 each year. The median delay from the first symptom to the time of diagnosis in the United States...