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A rare case of Takayasu’s arteritis presenting with stroke
Takayasu’s arteritis is a chronic inflammatory large vessel vasculitis of unknown aetiology that commonly affects women of child bearing age. It appears to have an acute early phase, with non- specific symptoms such as hypertension, headache, fever ...
P Siva Teja +5 more
doaj +1 more source
Takayasu arteritis in children [PDF]
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.
DÜZOVA, ALİ +14 more
openaire +9 more sources
Successful Pregnancy in a Patient with Takayasu’s Arteritis: a Case Report [PDF]
Takayasu’s arteritis, so-called pulseless disease, is a syndrome mostly seen in young women. It is a chronic inflammatory arteritis affecting large vessels. It is associated with abnormal angiography of the upper aorta and its main branches, resulting in
Z Ebrahimi, Z Khalaji Nia
doaj +1 more source
Sudden Death in a Child: The Mystery Behind the Cardiac Mass [PDF]
A 12-year-old boy suddenly collapsed while playing and was brought to the emergency department, where he was declared dead. The child had no prior medical illness.
Neethu Tony Mampilly +3 more
doaj +1 more source
Atherosclerosis in Takayasu arteritis [PDF]
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
Is Takayasu's arteritis more severe in children?
Objective. Takayasu's arteritis (TAK) is a chronic vasculitis, affecting predominantly the aorta and/or its major branches.
Sag, ERDAL +13 more
core +1 more source
Lack of Antilipoprotein Lipase Antibodies in Takayasu's Arteritis
Background. Antilipoprotein lipase (anti-LPL) antibodies were described in rheumatic diseases. In systemic lupus erythematosus they were highly associated with inflammatory markers and dyslipidemia, and may ultimately contribute to vascular damage.
Jozélio Freire de Carvalho +4 more
doaj +1 more source
Stroke as the initial presentation of Takayasu's arteritis: A case report
In this study, we report the case of a pediatric neurology stroke patient who was ultimately diagnosed with Takayasu's Arteritis. Our case describes a 14-year-old Hispanic female with no significant past medical history who presented to an outside ...
Paran Davari, BS +2 more
doaj +1 more source
Chorea: A rare manifestation of Takayasu's arteritis [PDF]
The case of a girl with recurring chorea and a Takayasu's arteritis diagnosis is reported. This clinical manifestation has been reported in only one patient with this vasculitis in the pediatric ...
Len, Claudio Arnaldo +4 more
core +1 more source
Takayasu's arteritis and secondary membranous nephropathy: an exceptional association
The association between Takayasu's arteritis and membranous nephropathy is uncommon. We present the case of a 46-year-old man with Takayasu's arteritis treated over 10 years by a multidisciplinary medical team.
Hernandez, Mariel +3 more
core +1 more source

