Title of article :
Flourine-18 flourodeoxyglucose Positron Emission Tomography as a non-invasive test of disease activity in Takayasuʹs arteritis — A report of four cases
Author/Authors :
Evan Glenn S. Vista، نويسنده , , Paul V. Santos Estrella، نويسنده , , Juan Javier T. Lichauco، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2010
Pages :
4
From page :
503
To page :
506
Abstract :
Background Takayasuʹs arteritis (TA) is a rare disease affecting the large arteries, particularly the aorta. Standard test to demonstrate abnormal vascular anatomy is angiography. This invasive procedure is limited in differentiating inflammatory and fibrotic lesions. Acute phase reactants have shown to have poor sensitivity and specificity in confirming disease activity in TA patients. Fluorine-18 flourodeoxyglucose Positron Emission Tomography (FDG-PET) scan has been utilized to detect areas of active inflammation in neoplastic, infectious and recently, vasculitic conditions. Objective To describe the FDG-PET scan findings of patients with Takayasuʹs arteritis. Methods This is a case series of four patients fulfilling the American College of Rheumatology classification criteria for TA. They were evaluated with FDG-PET scan to establish disease activity in correlation with other clinical and laboratory features. Results Three out of four patients showed evidence of increased radiotracer uptake in the aorta. Of these three patients, one had increased radiotracer uptake in the lungs secondary to active pulmonary tuberculosis. Conclusion PET scan is a promising but non-specific tool that provides clinicians with a non-invasive measure of disease activity in TA patients. Further studies confirming its utility in monitoring disease activity and response to treatment is recommended.
Keywords :
Takayasuיs arteritisFluorine-18 flourodeoxyglucosePositron Emission TomographyAngiographyAcute phase reactantTuberculosis
Journal title :
Autoimmunity Reviews
Serial Year :
2010
Journal title :
Autoimmunity Reviews
Record number :
475163
Link To Document :
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