9. An unusual case of Takayasu arteritis presenting as leptomeningitis with obstructive hydrocephalus

Tanna, Dhaval; Mendiratta, Naval; Negalur, Natasha

doi:10.1093/rap/rky033.001

Cited by 2 publications

(3 citation statements)

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“…TA was first described by an ophthalmologist, Dr Mikito Takayasou in 1908 [6] . TA is a recognized, but rare form of large vessel vasculitis with high prevalence in countries such as India and Japan [ 3 , 7 ]. TA is also known as the “pulseless disease” or “aortic arch syndrome” and is thought to be of autoimmune origin [4] .…”

Section: Discussionmentioning

confidence: 99%

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An unusual case of Takayasu arteritis presenting with persistent cough in a young female patient: A case report

Ameerah,

Moghrabi,

Awadghanem

et al. 2024

Radiology Case Reports

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Section: Discussionmentioning

confidence: 99%

“…TA is also known as the “pulseless disease” or “aortic arch syndrome” and is thought to be of autoimmune origin [4] . It is 10 times more common in females than in males of 10-40 years of age [7] . There are 6 cases of TA per 1000 people worldwide.…”

Section: Discussionmentioning

confidence: 99%

An unusual case of Takayasu arteritis presenting with persistent cough in a young female patient: A case report

Ameerah,

Moghrabi,

Awadghanem

et al. 2024

Radiology Case Reports

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“…Rare manifestations of Takayasu's arteritis include brain leptomeningitis, intracranial arteritis, and pyodermagangrenosum. [20][21][22] Recently there has been interest in the role of MRI in Takayasu arteritis as it can detect very early mural changes with better sensitivity and can give useful information about disease activity. 23 [18F]-Fluorodeoxyglucose positron emission tomography has also been proposed to evaluate response to treatment in Takayasu arteritis.…”

Section: Other Miscellaneous Findingsmentioning

confidence: 99%

Imaging Spectrum of Pediatric Nonspecific Aortoarteritis on CT Angiography: A Retrospective Study

Verma

Kumar

Aggarwal

et al. 2019

ANAMS

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Introduction Takayasu’s arteritis, a chronic, idiopathic, inflammatory panarteritis, is the major cause of Aortoarteritis in pediatric age group. The purpose of this study is to analyze the patterns of involvement and imaging findings of pediatric Takayasu’s arteritis. Materials and Methods We retrospectively reviewed the CT angiographic images of 11 pediatric cases reported as “Takayasu’s arteritis” or “nonspecific arteritis” over the period of last 3 years. Results Mural thickening with luminal stenosis was the most common findings. Aneurysmal dilatation of the descending thoracic aorta was observed in one case. Vessel stenoses without mural thickening, thrombosis and collateral vessel formation were the other findings. Pattern of involvement ranged from variable involvement of thoracic and abdominal aorta and their branches. Conclusion Awareness of its CT angiographic appearances and distribution pattern can help the clinicians and radiologists to have high index of suspicion in aiding early diagnosis and better management of this disease.

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9. An unusual case of Takayasu arteritis presenting as leptomeningitis with obstructive hydrocephalus

Cited by 2 publications

References 0 publications

An unusual case of Takayasu arteritis presenting with persistent cough in a young female patient: A case report

An unusual case of Takayasu arteritis presenting with persistent cough in a young female patient: A case report

Imaging Spectrum of Pediatric Nonspecific Aortoarteritis on CT Angiography: A Retrospective Study

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