Results 1 to 10 of about 5,162 (172)

Tuberculosis and Takayasu arteritis: a case report 

open access: yesJournal of Medical Case Reports, 2023
Background Takayasu arteritis is a rare and chronic granulomatous vasculitis that affects the large vessels. Takayasu arteritis targets the aorta and its branches and is still of unknown etiology. It often affects female patients under 50 years of age. A
Maryem Ferjani   +6 more
doaj   +1 more source

First case of childhood Takayasu arteritis from Syria: a case report

open access: yesJournal of Medical Case Reports, 2021
Background Takayasu arteritis is a systemic granulomatous inflammation affecting the large- and medium-sized vessels such as aorta, its main branches, and pulmonary and renal arteries.
Wafa Alwattar   +5 more
doaj   +1 more source

Concurrent coronary artery and subclavian arterial aneurysms in Takayasu arteritis

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2021
Background Aneurysmal coronary artery involvement and subclavian artery aneurysm are extremely uncommon in Takayasu arteritis. Case presentation We present a case with concurrent coronary artery and subclavian artery aneurysms.
Anoop Ayyappan   +2 more
doaj   +1 more source

Clinical Features of Aortitis with Gastrointestinal Involvement

open access: yesReviews in Cardiovascular Medicine, 2022
Few vascultides have a predilection for the aorta. Among those are Takayasu arteritis, Behcet’s disease, giant cell arteritis, and infectious aortitis.
Mansour Altuwaijri, Abdulmajeed Altoijry
doaj   +1 more source

Acute myocardial infarction with left main coronary artery ostial negative remodelling as the first manifestation of Takayasu arteritis: a case report

open access: yesBMC Cardiovascular Disorders, 2021
Background Takayasu arteritis is a chronic inflammatory disease involving the aorta and its major branches. Acute myocardial infarction rarely but not so much presents in patients with Takayasu arteritis, and the preferable revascularization strategy is ...
Shiqiang Zhou, Chao Gao, Fei Li
doaj   +1 more source

Takayasu arteritis in pregnancy: A case series [PDF]

open access: yesPerspectives In Medical Research, 2020
Takayasu arteritis is a disease of unknown etiology which is a primary systemic vasculitis leading to stenotic and occlusive changes. Takayasu arteritis is a chronic inflammatory disease in progressive pattern which chiefly affects the aorta and its ...
Ipsita Mohapatra1 , Subha Ranjan Samantaray1 ,G Priyanka2 , Achanta Vivekananda1
doaj   +1 more source

Visual loss in Takayasu Arteritis – Look Beyond the Eye [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2014
Patients with Takayasu arteritis often present with reduced vision related either to the disease per se or due to complications of therapy. We report a patient with Takayasu arteritis who developed acute onset bilateral visual loss 6wks following ...
Jayanthi Peter   +3 more
doaj   +1 more source

Spectrum of imaging findings in Takayasu arteritis—A case report

open access: yesRadiology Case Reports, 2022
Takayasu arteritis (TA) is an uncommon chronic granulomatous inflammatory disease often affecting the aorta and its branches. Early diagnosis is quite challenging due to nonspecific symptoms and unfamiliarity with the disease. We hereby present a case of
Kritisha Rajlawot, MD   +3 more
doaj   +1 more source

Takayasu arteritis and primary sclerosing cholangitis: A casual association or different phenotypes of the same disease?

open access: yesJournal of Translational Autoimmunity, 2021
Takayasu arteritis and primary sclerosing cholangitis are two rare disorders. The pathogenesis of Takayasu arteritis involves immune-mediated mechanisms, and corticosteroids represent the mainstay for treatment.
Giacomo Mulinacci   +4 more
doaj   +1 more source

Case report on rare case of dilated cardiomyopathy in young girl

open access: yesMedical 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

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