scholarly journals Severe Takayasu's arteritis of the pulmonary arteries: Report of a case with successful surgical treatment

1985 ◽  
Vol 5 (2) ◽  
pp. 369-373 ◽  
Author(s):  
John W. Moore ◽  
Michael J. Reardon ◽  
Denton A. Cooley ◽  
Thomas A. Vargo
2019 ◽  
Vol 107 (6) ◽  
pp. e375-e377
Author(s):  
Hee Jung Kim ◽  
Hyun Jong Lee ◽  
Jae Suk Yoo ◽  
Dong Jin Kim ◽  
Kwang Lee Cho

2018 ◽  
Vol 44 (2) ◽  
pp. 109-112
Author(s):  
Mohd Zahid Hussain ◽  
Md. Tariqul Islam ◽  
Tahmina Karim ◽  
Shakhawat Alam ◽  
Mostafizur Rahman Bhuiyan ◽  
...  

Takayasu arteritis (TA), also known as idiopathic medial aortopathy or pulseless disease, is a granulomatous large vessel vasculitis that predominantly affects the aorta and its major branches. It may also affect the pulmonary arteries. The exact cause is not well known but the pathology is thought to be similar to giant cell arteritis. There is segmental and patch granulomatous inflammation of the aorta which results in stenosis, thrombosis and aneurysm formation. Half of the patients present with an initial systemic illness whereas the other 50% present with late-phase complications. There is a strong female predominance (F: M ~ 9:1), an increased prevalence in Asian populations, and it tends to affect younger patients (<50 years of age). The typical age of onset is at around 15-30 years of age. Here, it is reported a case of 9 years old girl with Takayasu’s arteritis.


2004 ◽  
Vol 13 (3) ◽  
pp. 75
Author(s):  
T. Miyata ◽  
O. Sato ◽  
H. Koyama ◽  
H. Shigematsu ◽  
Y. Tada

2011 ◽  
Vol 9 (03) ◽  
pp. 194-197 ◽  
Author(s):  
Motomi Ando ◽  
Yutaka Okita ◽  
Yoshikado Sasako ◽  
Soichiro Kitamura ◽  
Hiroshi Matsuo

2011 ◽  
Vol 41 (3) ◽  
pp. 461-470 ◽  
Author(s):  
Kohava Toledano ◽  
Ludmila Guralnik ◽  
Avraham Lorber ◽  
Amos Ofer ◽  
Mordechai Yigla ◽  
...  

2010 ◽  
Vol 13 (3) ◽  
pp. 202-207 ◽  
Author(s):  
Motomi Ando ◽  
Yoshio Kosakai ◽  
Yutaka Okita ◽  
Kiyoharu Nakano ◽  
Soichiro Kitamura

2021 ◽  
Vol 26 ◽  
pp. 4345
Author(s):  
D. A. Grabovyi ◽  
J. V. Dzhinibalaeva ◽  
E. V. Adonina ◽  
D. V. Duplyakov

Takayasu's arteritis is a chronic granulomatous vasculitis of large vessels of unclear etiology, predominantly affecting the aorta and its main branches, with possible involvement of the coronary and pulmonary arteries. The true prevalence of this disease is unknown, but it is extremely low, given the rare diagnosis and the absence of pathognomonic symptoms. In clinical practice, the criteria proposed by the American College of Rheumatology are used for making a diagnosis. A wide range of imaging diagnostic techniques plays a significant role. This article provides a literature review and a case report of Takayasu's arteritis in a patient admitted with an acute coronary syndrome.


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