background: takayasu arteritis is a granulomatous vasculitis which mainly involves the large arterial vessels. the disease is rare and it is more common in females aged between 15-30 years old. in this paper, we report a case of takayasu arteritis in babol, north of iran. case presentation: a 22 - year old female was admitted to the department of infectious diseases of rouhani teaching hospital...

INTRODUCTION Giant cell arteritis is the most common form of large-vessel vasculitides. However, it is probable that extracranial involvement is underdiagnosed in patients with classical giant cell arteritis. In the recent literature most cases of giant cell arteritis have been described in conjunction with aortic aneurysms or dissections. Nonetheless the coexistence of giant cell arteritis and...

A 44-year-old housewife was found to have coarctation of the abdominal aorta secondary to Takayasu's arteritis. Since she also had mitral stenosis, possible etiological relation between Takayasu's arteritis and mitral stenosis is suspected.

Cogan's syndrome may be associated with large-vessel arteritis. We describe a patient with ocular inflammation, sensorineural hearing loss and arm claudication in whom a diagnosis of 'atypical' Cogan's syndrome and Takayasu's arteritis was made. All symptoms resolved with treatment.

takayasu’s arteritis (ta) is a rare case of granulomatous arteritis which mainly involves the aorta and its large branches. although arterial hypertension is the most common feature of the disease in both adults and children, patients with ta may present with numerous clinical manifestations. our patient was a 45-year-old woman, known to have hypertension from 3 years earlier following assessme...

neurological manifestation may complicate takayasu arteritis (ta). a 23-year-old girl with sudden onset of vision loss was admitted to hospital. her brain mri showed abnormal t2-signal hyperintensity and visual evoked potential revealed prolonged p100 latency. consequently, optic neuritis was diagnosed. a review on history of dizziness, falling, and weak pulses of upper extremities led to more ...

BACKGROUND Takayasu arteritis and ulcerative colitis are immune-mediated inflammatory diseases; genetic factors are assumed to play an important role in the pathogenesis of these 2 diseases. However, the coexistence of these 2 diseases has rarely been reported. CASE REPORT In this report, we present a rare case of a 29-year-old man with a 4 years history of ulcerative colitis who developed Ta...

Progressive degenerative changes in ageing temporal arteries are described. These changes are usually severe in elderly patients, hence their presence in diagnostic biopsies provides no evidence of temporal arteritis past or present. In two patients in the series of random necropsies examined there were changes in the temporal arteries identical with those seen in patients known to have suffere...

BACKGROUND AND PURPOSE The frequency and amount of intracranial, intradural inflammatory vessel wall enhancement in giant cell arteritis remain unclear. The purpose of this work was to prospectively assess the intracranial extent of vasculitic changes in patients with giant cell arteritis using a dedicated MR imaging protocol optimized for assessment of mural changes of intracranial arteries. ...

Takayasu arteritis is a vasculitic condition which affects large and medium sized vessels primarily aorta its main branches. It rare affecting females more than males between 10 40 years of age with spectrum clinical presentation. Here we present case 58 year old man who presented to us non-specific gastrointestinal symptoms was eventually diagnosed arteritis.