Results 11 to 20 of about 3,553 (227)
Frontiers in Pediatrics, 2018 La arteritis de Takayasu es una vasculitis granulomatosa idiopática de la aorta y sus ramas principales. Es más frecuente entre los asiáticos y las mujeres, y constituye una de las vasculitis más comunes en los niños. La inflamación y la proliferación de la íntima conducen al engrosamiento de la pared, lesiones estenóticas u oclusivas y trombosis ...
Ricardo Russo, María M. Katsicas
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SAGE Open Medical Case Reports, 2023 Type I Takayasu’s arteritis is a rare form of large vessel vasculitis with an unknown etiopathogenesis. It is characterized by progressive chronic inflammation and occlusive thromboaortopathy affecting the aorta and its main branches.
Caner Arslan +2 more
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IHJ Cardiovascular Case Reports, 2022 Stent thrombosis following percutaneous trans-luminal renal angioplasty [PTRA] for renal artery involvement secondary to Takayasu's arteritis is a serious medical emergency, requiring early detection and urgent intervention to prevent permanent kidney ...
Pankaj Jariwala +3 more
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Scandinavian Journal of Rheumatology, 2005 Introduction. Giovanni Battista Morgani reported the first case with Takayasu arteritis (TA) in 1761. The disease affects the aortic arch and large blood vessels. It is found in every race and in every age-group, predominantly in female population aged 20-40 years.
Sidor, Misović +3 more
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Surgical repair of an aortico-left ventricular tunnel with Takayasu's arteritis
Journal of Cardiothoracic Surgery, 2022 Aortico-left ventricular tunnel is a very rare congenital cardiac anomaly, always arises from the right coronary sinus and enters the left ventricle. However, aortico-left ventricular tunnel associated with Takayasu's arteritis has not been described so ...
Runqian Sui +3 more
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The Journal of the American Osteopathic Association, 1989 Takayasu's arteritis, an inflammatory and obliterative disease of medium and large arteries, is classified as a giant cell arteritis. It has a predilection for the aortic arch and its branches and the pulmonary arteries. Unlike atherosclerotic vascular diseases, Takayasu's arteritis affects young women primarily.
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Pyoderma Gangrenosum and Erythema Nodosum Revealing Takayasu’s Arteritis
Case Reports in Dermatology, 2016 We report a Caucasian female who presented with simultaneous erythema nodosum and pyoderma gangrenosum due to underlying Takayasu’s arteritis. Takayasu’s arteritis is a chronic large vessel vasculitis of unknown cause.
Jonas Loetscher +2 more
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Takayasu's arteritis associated with Crohn's disease: a case report
Journal of Medical Case Reports, 2008 Introduction The simultaneous presence of Takayasu's arteritis and Crohn's disease in a patient seems to be rare. To our knowledge, no patient with the combination of Crohn's disease and Takayasu's arteritis has been reported from our region.
Daryani Nasser E +6 more
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Recovery from repeated sudden hearing loss in a patient with Takayasu’s arteritis treated with hyperbaric oxygen therapy: the first report in the literature [PDF]
, 2017 Hearing loss has been rarely reported in Takayasu's arteritis, presents as sudden sensorineural hearing loss and usually responds well to corticosteroid therapy.
ALTISSIMI, Giancarlo +8 more
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Takayasu arteritis in children [PDF]
Pediatric Rheumatology, 2008 Abstract Takayasu arteritis (TA) is a large vessel vasculitis that usually affects young female patients during the second and third decades of life, but has been reported in children as young as 24 months of age. Aim of this report was to describe four children (two girls) with TA, as well as summarizing main published studies.
Yalcinkaya, Fatos +14 more
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