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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease arteritis, giant cell
Comorbidity C0042384|vasculitis
Sentences 5
PubMedID- 23456154 By transoesophageal echocardiography and combined 18f-fluordeoxyglucose positron emission and ct (18f-fdg pet/ct), the diagnosis of large artery vasculitis owing to giant cell arteritis was confirmed.
PubMedID- 25992164 The most common indication for the test was lung cancer (7 cases, corresponding to 43.75%), followed by breast cancer (3 cases), giant cell vasculitis (1 case each of horton disease and takayasu arteritis), and 1 case each of locally advanced oropharyngeal cancer, gallbladder carcinoma with liver metastasis, peritoneal carcinomatosis of gynecologic origin, and retroperitoneal lymphoma.
PubMedID- 25147009 Lower extremity vasculitis in giant cell arteritis: important differential diagnosis in patients with lower limb claudication.
PubMedID- 20734595 Primary vasculitis included horton disease in 3 cases, wegener disease in 2, takayasu disease in 1, and buerger disease in 1.
PubMedID- 21586202 This review focuses on morphologic aspects of large-vessel vasculitis pathology associated with giant cell arteritis, takayasu arteritis, idiopathic or isolated aortitis, lymphoplasmacytic thoracic and ascending aortitis, and the inflammatory aneurysm/retroperitoneal fibrosis syndrome.

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