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Takayasu arteritis is a rare, systemic, inflammatory large-vessel vasculitis of unknown etiology that most commonly affects women of. Takayasu arteritis (TA), also known as idiopathic medial aortopathy or pulseless disease, is a granulomatous large vessel vasculitis that predominantly affects. Takayasu arteritis is a chronic, idiopathic, inflammatory disease that primarily affects large vessels, such as the aorta and its major branches and the pulmonary.

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The thickening of the entire vessel wall results in stiffness, and this is the primary sign identified using imaging The differential diagnoses should include common diseases such as atherosclerosis, giant cell arteritis takayasi polyarteritis nodosa. In the Western worldatherosclerosis is a more taksyasu cause of obstruction of the aortic arch vessels than Takayasu’s arteritis.

Case 7 Case 7. In view of the chronic process and good collateral development, Raynaud’s phenomenon or digital gangrene are very rare in Takayasu arteritis. Case 5 Case 5. Angiography provides information on vessel anatomy and patency but does not provide information on the degree of inflammation in the wall.

The characteristic finding is the xrterite of “skip lesions,” where stenosis or aneurysms alternate with normal vessels. Takayasu’s arteritis, dissection, inflammation, stenosis, ischemia. The treatment of TA begins with pharmacological control of the acute arteritis in order to induce clinical remission, followed by treatment of vascular abnormalities 2.

There are often reduced or absent peripheral pulses, giving rise to its alternative name of “pulseless disease”.

Diagnostic criteria for Takayasu arteritis. Korean J Radiol ; 8: Polyarteritis nodosa frequently occurs in adults who are 30—50 years old, affecting males more than females, and it also more commonly affects patients with hepatitis B. Pulseless disease Takayasu syndrome Takayasu disease Aortic arch syndrome Takayasu’s arteritis Aortoarteritis.


The diagnosis of TA is still a challenge for clinicians, although several diagnosis criteria have been proposed to improve the early diagnosis [ 111 ]. A year-old female Takayasu takayask patient with syncope, dyspnoea, and shortness of breath for 4 months, and left limb claudication for 3 months.

The non-specific inflammation of involved vessels usually leads to concentric wall thickening, takayaeu and thrombus formation.

Differential diagnosis The differential diagnoses should include common diseases such as atherosclerosis, giant cell arteritis and polyarteritis taakyasu. TA is a rare clinical condition that is characterized by chronic panarteritis of the aorta and its primary branches, including the subclavian, common carotid, coronary and renal arteries, and may result in localized stenoses, vascular occlusion, dilatation and aneurysm formation 8. The American College of Rheumatology criteria for the classification of Takayasu’s arteritis.

Characteristic signs and symptoms of at least one month duration a.

These limitations prevent these two modalities from being the ideal methods in the serial evaluation of TA patients [ 1019 ].

For evaluation of the systemic large-artery involvement, computed tomographic angiography using ioversol contrast adterite 20 ml; Jiangsu Hengrui Medicine Co. Axial images allow accurate evaluation of the arterial wall thickness and calcification. Carotid lesions detected by B-mode ultrasonography in Takayasu’s taakayasu China Find articles by Lei Zhou.

Neurological symptoms in type A aortic dissections.

Vaideeswar P, Deshpande JR. Unable to process the form. Acute hemorrhagic edema of infancy Cryoglobulinemic vasculitis Bullous small vessel vasculitis Cutaneous small-vessel vasculitis. However, the incidence of arteirte in arteries is low.

This phase gradually resolves with the initiation of the chronic phase which is characterised by artdrite and obliterative changes in the aorta and its branches. Those with the disease often notice symptoms between 15 and 30 years of age. Although the cause of Takayasu arteritis is unknown, the condition is characterized by segmental and patchy granulomatous inflammation of the aorta and its major derivative arteirte.


Histopathology reveals TA as granulomatous panarteritis characterized by T lymphocytes, B lymphocytes, macrophages and multinucleated giant cells infiltration of the arterial wall [ 13 ]. National Takyasu for Biotechnology InformationU. A year-old male with Takayasu arteritis. Takayasu’s arteritis involving the pulmonary arteries: A year-old female patient diagnosed with Takayasu arteritis with a complaint of hypertension for 1 year.

Takayasu arteritis: imaging spectrum at multidetector CT angiography

Views Read Edit View history. A number of studies have suggested that patients with artery dissection may have a genetically-determined weakness of the vessel wall, and that environmental factors, such as acute infection or minor trauma, may serve as triggers 12 — N Engl J Med ; In conclusion, as arteirte of the si causes of ischemic stroke in young adults, artery dissection requires early identification and management China Find articles by Nan Kang. In this article, we will review the CTA findings in TA and how this non-invasive method impacts patient care.

China Find articles by Ruonan Hao. Calcification in ascending aorta can be observed in some TA patients, but it is rare in atherosclerosis.

Takayasu’s arteritis

Diseased arteries become stenotic or occluded, undergo vascular remodelling or develop aneurysms. Onishi and Kagoshima reported similar eye findings in individuals whose wrist pulses were absent. With luminal narrowing, collateral vessels may be observed in some cases.

In patients with symptomatic stenotic or occlusive lesions, percutaneous transluminal angioplasty and stenting or bypass surgery is the most common palliative treatment [ 12 ].