Related Experiment Video
Updated: Jun 17, 2026

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Abstract:
Idiopathic vasculitides are systemic inflammatory diseases of vessels, chiefly arteries, of all sizes. The etiology of most vasculitides is unknown. Some are infectious, others involve the deposition of circulating immune complexes in vessel walls. Diagnosis is a composite of clinical symptoms and signs, serologies, histopathology, clinical course and response to therapy. Seven main groups of idiopathic vasculitides have been identified: Overlap syndromes are not uncommon, however, as classification is artificial inasmuch it is based more on consensus than on actual biological features. Giant cell (temporal) arteritis is a systemic inflammatory disease of the aorta and its major branches, especially extracranial arteries. Its etiology and pathogenesis are largely unknown. Elderly persons of Nordic descent, chiefly women, are primarily affected.
Related Concept Videos
Cerebral Edema ll: Pathophysiology
Vascular Spasm
Rheumatic Heart Disease I: Introduction
Autoimmune Disorders
Concept and Mechanism of Autoimmune Diseases
The immune system...
Cytotoxic Edema: Pathophysiology
Endocarditis II: Clinical Features of Infective Endocarditis

