Results 21 to 30 of about 5,412 (184)

Takayasu arteritis with pyoderma gangrenosum: case reports and literature review

open access: yesBMC 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
doaj   +1 more source

The angiographic and clinical profile of patients with Takayasu aortoarteritis

open access: yesHeart Vessels and Transplantation, 2023
Objective: Takayasu arteritis is a rare, chronic, inflammatory disease that primarily affects the aorta and its major branches. It mainly affects young females, and it can cause significant morbidity and mortality if untreated.
Jitendra Sharma   +7 more
doaj   +1 more source

Bronchiectasis and hoarseness of voice in takayasu arteritis: a rare presentation

open access: yesBMC Research Notes, 2012
Background Takayasu arteritis is a large vessel vasculitis occurring in young females. We report a rare presentation of Takayasu arteritis in a Sri Lankan woman.
ND Perera Gamage   +3 more
doaj   +1 more source

Aortic valve replacement surgery for a case of infantile Takayasu arteritis [PDF]

open access: yesKorean Journal of Pediatrics, 2012
Takayasu arteritis is a chronic inflammatory disease of unknown etiology primarily affecting the aorta and its major branches and usually occurring in the second or third decade of life.
Hye Won Kwon   +7 more
doaj   +1 more source

An unusual collateral from the sinoatrial nodal artery to the left carotid artery in a patient with Takayasu arteritis: a case report

open access: yesJournal of Medical Case Reports, 2023
Background Takayasu arteritis is a noninfective chronic vasculitis mainly involving the aorta and its main branches. The presentation of the disease is heterogeneous, ranging from asymptomatic to catastrophic illness.
Marcel A. Beijk, R. Nils Planken
doaj   +1 more source

Takayasu arteritis: clinical importance of extra-vessel uptake on FDG PET/CT

open access: yesEuropean Journal of Hybrid Imaging, 2019
Background [F-18]fluorodeoxyglucose positron emission tomography/computed tomography is routinely used for assessing Takayasu arteritis patients. However, extra-vessel [F-18]fluorodeoxyglucose uptake has not been evaluated in detail in these patients. We
Junichi Tsuchiya   +8 more
doaj   +1 more source

The genetics of Takayasu arteritis [PDF]

open access: yesLa Presse Médicale, 2017
Takayasu arteritis (TAK) is a rare systemic vasculitis that is characterized by granulomatous inflammation of the aorta and its major branches. The cellular and biochemical processes involved in the pathogenesis of TAK are beginning to be elucidated, and implicate both cell and antibody-mediated autoimmune mechanisms.
Paul, Renauer, Amr H, Sawalha
openaire   +2 more sources

Regressed coronary ostial stenosis in a young female with Takayasu arteritis: a case report

open access: yesBMC Cardiovascular Disorders, 2019
Background Takayasu arteritis is a rare systemic vasculitis, which affects the aorta and its major branches, especially in young females. Diagnosis and treatment for Takayasu arteritis with coronary stenosis are important to prevent fatal complications ...
Tetsuro Yokokawa   +10 more
doaj   +1 more source

Atherosclerosis in Takayasu arteritis [PDF]

open access: yesAnnals of the Rheumatic Diseases, 2006
Chronic inflammatory diseases such as systemic lupus erythematosus (SLE) and rheumatoid arthritis are associated with accelerated atherosclerosis. We hypothesised that atherosclerosis may also be increased in Takayasu arteritis.The frequency of atherosclerotic plaques and the intima-media thickness (IMT) were investigated in 30 female patients with ...
Seyahi, E   +6 more
openaire   +3 more sources

Severe ADEM‐Like Neuroinflammatory Disease and Cerebrovascular Fragility With Recurrent Pseudoaneurysms and Moyamoya in a Familial Germline CBL Mutation: Expanding the Clinical Phenotype

open access: yesAmerican 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

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