Aortitis pathophysiology: Difference between revisions
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==Overview== | ==Overview== | ||
Aortitis is | Aortitis is a term used to describe inflammation of the aortic wall. The majority of cases of bacterial aortitis are due to bacteria seeding through a segment of the aortic wall with existing pathology via the vasa vasorum. Tuberculous aortitis occurs due to miliary spread or as a result of direct seeding of the thoracic aorta from adjacent infected tissues. Syphilitic aortitis most commonly involves the ascending aorta. | ||
Syphilitic or luetic aortitis, now exceedingly rare, typically involves the ascending aorta and is associated with thoracic aortic aneurysm. The classic histopathological finding is “tree barking” of the aortic intima.2 A chronic inflammatory infiltrate of the medial and adventitial vasa vasorum is present, which ultimately leads to medial necrosis and a wrinkled appearance of the intima. | |||
Both GCA and Takayasu arteritis are associated with an inflammatory cellular infiltrate of the aortic media, adventitia, and vasa vasorum that contains a predominance of lymphocytes, macrophages, and multinucleated giant cells.2,3 Over time, scarring of the aortic media and destruction of the elastic lamina occur.2,3 Tree barking may be seen in both of these disorders, not just in syphilis-associated aortitis | |||
Granuloma formation and multinucleated giant cells may be seen in both GCA and Takayasu arteritis | |||
Takayasu arteritis is more commonly associated with extensive intimal and adventitial fibrosis or scarring with resultant luminal narrowing.2,4,5 Aortic wall thickness generally is greater among patients with Takayasu aortitis than GCA.2,5 GCA is more commonly associated with extensive medial inflammation and necrosis and the formation of aortic aenurysms. | |||
GCA has been associated with HLA-DR4, whereas Takayasu arteritis has been associated with HLA-BW52, HLA-DR2, and HLA-MB1 in Japanese patients and possibly with HLA-DR4 in non-Asian patients. | |||
aortitis has been reported in the HLA-B27–associated seronegative spondyloarthropathies Reiter syndrome and ankylosing spondylitis. | |||
==References== | ==References== | ||
Revision as of 15:44, 10 September 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]
Overview
Aortitis is a term used to describe inflammation of the aortic wall. The majority of cases of bacterial aortitis are due to bacteria seeding through a segment of the aortic wall with existing pathology via the vasa vasorum. Tuberculous aortitis occurs due to miliary spread or as a result of direct seeding of the thoracic aorta from adjacent infected tissues. Syphilitic aortitis most commonly involves the ascending aorta.
Syphilitic or luetic aortitis, now exceedingly rare, typically involves the ascending aorta and is associated with thoracic aortic aneurysm. The classic histopathological finding is “tree barking” of the aortic intima.2 A chronic inflammatory infiltrate of the medial and adventitial vasa vasorum is present, which ultimately leads to medial necrosis and a wrinkled appearance of the intima.
Both GCA and Takayasu arteritis are associated with an inflammatory cellular infiltrate of the aortic media, adventitia, and vasa vasorum that contains a predominance of lymphocytes, macrophages, and multinucleated giant cells.2,3 Over time, scarring of the aortic media and destruction of the elastic lamina occur.2,3 Tree barking may be seen in both of these disorders, not just in syphilis-associated aortitis
Granuloma formation and multinucleated giant cells may be seen in both GCA and Takayasu arteritis
Takayasu arteritis is more commonly associated with extensive intimal and adventitial fibrosis or scarring with resultant luminal narrowing.2,4,5 Aortic wall thickness generally is greater among patients with Takayasu aortitis than GCA.2,5 GCA is more commonly associated with extensive medial inflammation and necrosis and the formation of aortic aenurysms.
GCA has been associated with HLA-DR4, whereas Takayasu arteritis has been associated with HLA-BW52, HLA-DR2, and HLA-MB1 in Japanese patients and possibly with HLA-DR4 in non-Asian patients.
aortitis has been reported in the HLA-B27–associated seronegative spondyloarthropathies Reiter syndrome and ankylosing spondylitis.