aortitis/maumivu ya kichwa

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14 matokeo

[Ruptured cerebral aneurysm associated with aortitis syndrome: a case report].

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Ingia / Ingia

In rare occasions, patients with aortitis syndrome have cerebral aneurysms and only seven cases have been reported so far. A case of aortitis syndrome complicated with basilar bifurcation aneurysm is reported. A 58-year-old woman, who had been hypertensive for 20 years and was diagnosed as pulseless

[A case of aortitis syndrome associated with basilar aneurysm (author's transl)].

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Ingia / Ingia

A case of aortitis syndrome (pulseless disease) associated with basilar aneurysm is reported. This patient was 52-year-old woman suffering from pulseless disease for past fifteen years. She was admitted to our hospital with severe headache, nausea and vomiting. Four vessel angiograms revealed an

Takayasu's Arteritis Presenting with Headache and Peripheral Facial Palsy: A Case Report.

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Ingia / Ingia

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

[Aneurysm of anterior communicating artery associated with aortitis syndrome--a treated case by aneurysmal neck clipping (author's transl)].

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Ingia / Ingia

A rare case of the cerebral aneurysm associated with aortitis syndrome was reported. It seems to be the first case in which neck clipping was successfully performed for aneurysm of the anterior communicating artery. The patient was a 48-year-old female afflicted with pulseless disease. She was

Successful Hybrid Neurovascular Surgery for a Ruptured Basilar Artery Dissecting Aneurysm in a Patient with Jeopardized Collateral Circulation Associated with Aortitis Syndrome.

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Ingia / Ingia

BACKGROUND Dissecting aneurysms of the basilar artery (BA) are rare lesions, and the management of them has been controversial and challenging. The treatment becomes much more difficult when the patient has a disorder such as aortitis syndrome, which makes cerebral arteries occluded and tortuous. We

[Pericardial effusion and aortitis: unusual main manifestations of giant cell arteritis].

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Ingia / Ingia

Giant cell arteritis is a systemic vasculitis with segmentary vascular localisation, usually manifesting as temporal arteritis (Horton's disease). The predominant localisation in different vascular districts leads to clinical heterogeneity and poses a considerable diagnostic challenge. We describe a

Low back pain as presenting manifestation of giant cell arteritis associated to abdominal aortitis.

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Ingia / Ingia

Giant cell arteritis (GCA) is the most common vasculitis in Western countries in individuals over the age of 50. The diagnosis is relatively straightforward when typical features, such as headache, jaw claudication or other ischemic complications are present. Although atypical presentations of GCA

Interstitial Keratitis, Vertigo, and Vasculitis: Typical Cogan's Syndrome.

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Ingia / Ingia

Cogan's syndrome (CS) is a chronic inflammatory disorder of unknown etiology that most commonly affects young adults. Clinical hallmarks are bilateral interstitial keratitis and vestibuloauditory dysfunction. Association between CS and systemic vasculitis as well as aortitis also exists. The

Development of Giant Cell Arteritis after Treating Polymyalgia or Peripheral Arthritis: A Retrospective Case-control Study.

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Ingia / Ingia

OBJECTIVE We investigated the development of giant cell arteritis (GCA) in patients with prior diagnoses of isolated polymyalgia rheumatica and/or peripheral arthritis (PMR/PA), and the potentially relevant characteristics of both illnesses in such patients. METHODS We retrospectively compared the

Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report.

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Ingia / Ingia

BACKGROUND 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

Takayasu arteritis with multiple intracranial aneurysms. A case report.

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Ingia / Ingia

CONCLUSIONS A rare case of multiple cerebral aneurysms associated with Takayasu aortitis is reported. Only seven cases have been reported so far, all of which are from Japan. This is the first case with this association being reported from India. A 50-year-old hypertensive woman developed sudden

Mega-aorta syndrome development in giant cell arteritis. A same entity?

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Ingia / Ingia

Giant cell arteritis (GCA) is the most common form of large vessel arteritis. GCA typically involves the branches of the external carotid artery, but is the leading cause of inflammatory aortitis. However, involvement of the aorta often goes undetected. We present a case of an 81-year-old man, with

Controversies regarding giant cell (temporal, cranial) arteritis.

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Ingia / Ingia

It is important to establish the diagnosis of temporal arteritis because the disease is treatable; treatment may prevent blindness and even death. Temporal arteritis usually occurs in people older than 51 years of age, although very rarely, histologically documented disease occurs in younger people.

Cogan syndrome: a retrospective review of 60 patients throughout a half century.

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Ingia / Ingia

OBJECTIVE To evaluate the disease manifestations and clinical course of patients affected by Cogan syndrome (a syndrome of nonsyphilitic interstitial keratitis and vestibuloauditory symptoms) at a single institution during roughly a half century. METHODS Medical records of all patients diagnosed as

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