Takayasu arteritis in childhood: retrospective experience from a tertiary referral centre in the United Kingdom. [PDF]
, 2015 Takayasu arteritis (TA) is an idiopathic large-vessel vasculitis affecting the aorta and its major branches. Although the disease rarely affects children, it does occur, even in infants.
Al-Obaidi, M +5 more
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Hearing loss in Takayasu's arteritis: a role for hyperbaric oxygen therapy? [PDF]
, 2017 In the scientific community, there is growing interest regarding associated symptoms in Takayasu’s arteritis (TA), an autoimmune condition that mainly affects the medium and large arteries.
de Vincentiis, Marco +2 more
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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
doaj +1 more source
Patterns of Arterial Disease in Takayasu Arteritis and Giant Cell Arteritis
Arthritis care & research, 2020 To identify and validate, using computer‐driven methods, patterns of arterial disease in Takayasu arteritis (TAK) and giant cell arteritis (GCA).
K. Gribbons +24 more
semanticscholar +1 more source
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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Insights into Imaging of Aortitis [PDF]
, 2012 Background: Aortitis is a subtype of the more general term “vasculitis”, an inflammatory condition of infectious or noninfectious origin involving the vessel wall.
Bankier, Alexander +2 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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Eosinophilic granulomatosis with polyangiitis (EGPA) and PRES: a case-based review of literature in ANCA-associated vasculitides [PDF]
, 2015 Eosinophilic granulomatosis with polyangiitis (EGPA) is a small-sized vessel systemic necrotizing vasculitis and belongs to the family of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides.
Barilaro, Giuseppe +3 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
doaj +1 more source