Horner syndrome as a manifestation of an exacerbation of Takayasu’s arteritis

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Horner syndrome as a manifestation of an exacerbation of Takayasu’s arteritis

Purpose Takayasu’s arteritis is a chronic, granulomatous, large vessel vasculitis affecting the aorta and its large branches, and occurring most commonly in young women. It is the third most frequently diagnosed vasculitis in childhood. Generally, symptoms reflect ischemia to an affected organ or limb. A small percentage of patients develop neurologic symptoms such as visual disturbances, trans...

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[Horner syndrome as a manifestation of carotid artery dissection].

CLINICAL CASE A 42-year-old man presented with ptosis and miosis in his left eye and a history of headache over the last 20 days. An angioresonance showed dissection of internal carotid artery. DISCUSSION "Painful Horner's Syndrome" is considered to be a medical emergency due possible onset of an internal carotid artery dissection. We consider that awareness of neuro-ophthalmologic emergencie...

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Horner syndrome as a manifestation of thyroid carcinoma: a rare association.

An 82-year-old patient presented a progressively growing hard thyroid nodule, and left ptosis. Additionally, ophthalmologic evaluation revealed ipsilateral miosis, diagnostic findings of Horner syndrome. Computerized tomography revealed a 7.5-cm thyroid mass infiltrating the main neck vessels. Although clinical and imaging data were suggestive of poorly differentiated thyroid carcinoma, fine-ne...

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Pre-pulseless and Pulseless Takayasus' Arteritis

The Confused Terminology and Changing Concept of Takayasu's Arteritis In 1908 the Japanese opihthalmologist, Takayasu, reported an unusual wreath-like vascular anastomosis surrounding the optic discs of a young female patient who was nearly iblind, biut who showed 'no general physical changes'. He was unalble to explain this abnormality. Laiter a colleague, Onishi, referred to a similar case wh...

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Pleural effusion as manifestation of temporal arteritis.

Two patients with temporal arteritis who presented with pleural effusion are reported. Both had an exudate that responded to prednisolone treatment.

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ژورنال

عنوان ژورنال: Pediatric Rheumatology

سال: 2012

ISSN: 1546-0096

DOI: 10.1186/1546-0096-10-s1-a84