Results 21 to 30 of about 7,975 (186)
Arterite de Takayasu: a propósito de um caso clínico
Revista Portuguesa de Cardiologia, 2015 Resumo: A arterite de Takayasu é uma vasculite de grandes vasos que cursa com apresentações clínicas diversas consoante os territórios afetados. Apresenta‐se o caso clínico de uma mulher de 47 anos a quem foi feito o diagnóstico de arterite de Takayasu ...
Bernardo Duque Neves +5 more
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Malignant Ischemic Stroke in a Young Female: A Rare Primary Manifestation of Takayasu Arteritis
Case Reports in Neurological Medicine, 2019 Takayasu arteritis is a rare chronic progressive granulomatous necrotizing large vessel panvasculitis mainly involving aorta and its main branches. It commonly affects the female in second to third decades.
Bhupendra Shah, Roshan Chhetri
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Case report on rare case of dilated cardiomyopathy in young girl
Medical Journal of Dr. D.Y. Patil University, 2015 Takayasu′s arteritis is a large vessel vasculitis in which the inflammatory process involves aorta and major branches. The cause is largely unknown. Dilated cardiomyopathy (DCM) is, however, reported to be seen in only 5-6% of cases of Takayasu arteritis.
Madhulika Mahashabde +3 more
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Emerging Concepts in the Evaluation and Management of Takayasu Arteritis:New Wine in an Old Bottle
JK Science, 2022 Takayasu arteritis is an enigmatic granulomatous large vessel vasculitis more common in the Indian scenario than in the West. Takayasu arteritis associates with impaired quality of life and also increases the risk of dying.
Durga Prasanna Misra, Vikas Agarwal
doaj
Takayasu arteritis with pyoderma gangrenosum: case reports and literature review
BMC Rheumatology, 2019 Background Takayasu arteritis is a rare, chronic inflammatory arteriopathy affecting mainly the aorta and its branches. Many skin manifestations have been reported in association with this disease.
Xuehan Zhang, Yang Jiao
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Acta chirurgica Iugoslavica, 2005 Surgical treatment of two female patients aged 32 and 41 years, with neurological problems causes by type I Takayasu?s aortoarteritis, are presented here. both of them were treated with by pass from ascending aorta to left common carotid and left subclavian arteries, using transsternal approach. During the follow up period (3.5 years for the first, and
L, Davidovic +4 more
openaire +3 more sources
Takayasu arteritis a cause of hypertensive disorder of pregnancy: a case report
Journal of Medical Case Reports, 2018 Background Takayasu arteritis is a rare, chronic, granulomatous systemic vasculitis of unknown etiology and a few cases have been reported in pregnancy. In pregnancies concomitant with Takayasu arteritis or after diagnosis, Takayasu arteritis negatively ...
Jesus Lumbreras-Marquez +3 more
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Management of Spontaneous Crystalline Lens Luxation in a Patient Diagnosed with Takayasu’s Disease
Diagnostics, 2023 Takayasu’s disease is a chronic granulomatous arteriopathy that affects large vessels and their major branches. Nonspecific symptoms characterize the early phase, whereas findings of arterial occlusion and aneurysmal formation become manifest later ...
Elvia Mastrogiuseppe +5 more
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Abnormal molecular response to Takayasu arteritis causing extensive large-vessel calcification
Journal of Vascular Surgery Cases and Innovative Techniques, 2016 Takayasu arteritis is a large-vessel vasculitis that often results in pulselessness due to fibrotic stenoses. Whereas minor calcification is sometimes seen with Takayasu arteritis, it rarely causes stenosis.
Brandon T. Garland, MD +5 more
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American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Heterozygous germline variants in CBL disrupt its function as a negative regulator of the Ras/MAPK pathway, classically predisposing to Juvenile myelomonocytic leukemia (JMML) and moyamoya. We describe two affected siblings carrying a paternally inherited CBL variant (c.1210 T> C, p.
Michal Bar‐Hakim +12 more
wiley +1 more source