Objective: To assess the histopathological findings of a large series of ascending thoracic aortic aneurysm (TAA) surgical specimens applying the updated classification on noninflammatory degenerative and inflammatory aortic diseases proposed by the Association for European Cardiovascular Pathology and the Society for Cardiovascular Pathology clinicopathological correlations. Methods: A total of 255 patients surgically treated for ascending TAA were enrolled. Surgical ascending aorta specimens were examined. Results: The histopathological substrate of ascending TAAs was mainly degenerative (67.5%), but with a remarkable prevalence of atherosclerotic lesions (18.8%) and aortitis (13.7%). Degenerative patients more frequently had bicuspid aortic valve (37.2%; P = .002). Patients in the atherosclerotic group were older (median age, 69 years; P < .001), more often with a history of hypertension (87.5%; P = .059), hypercholesterolemia (75%; P = .019), diabetes (16.6%; P = .054), current smoking (22.9%; P = .066), and a history of coronary artery disease (18.7%; P = .063). Patients with aortitis represented the older group (median age, 75 years, P < .001), were mostly females (68.6%; P < .001), and had a larger ascending aorta diameter (median, 56 mm; P < .001). Both patients with atherosclerosis and aortitis presented a higher incidence of concomitant abdominal aortic aneurysm (20.8% and 22.8%, respectively; P < .001). Conclusions: Although degenerative histopathology is the most frequent substrate in ascending TAA, atherosclerosis and inflammation significantly contribute to the development of chronic aortic thoracic disease.

Leone O., Corsini A., Pacini D., Corti B., Lorenzini M., Laus V., et al. (2020). The complex interplay among atherosclerosis, inflammation, and degeneration in ascending thoracic aortic aneurysms. THE JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 160(6), 1434-1443.e6 [10.1016/j.jtcvs.2019.08.108].

The complex interplay among atherosclerosis, inflammation, and degeneration in ascending thoracic aortic aneurysms

Corsini A.;Pacini D.;Lorenzini M.;Foa A.;Bacchi Reggiani M. L.;Di Marco L.;Rapezzi C.
2020

Abstract

Objective: To assess the histopathological findings of a large series of ascending thoracic aortic aneurysm (TAA) surgical specimens applying the updated classification on noninflammatory degenerative and inflammatory aortic diseases proposed by the Association for European Cardiovascular Pathology and the Society for Cardiovascular Pathology clinicopathological correlations. Methods: A total of 255 patients surgically treated for ascending TAA were enrolled. Surgical ascending aorta specimens were examined. Results: The histopathological substrate of ascending TAAs was mainly degenerative (67.5%), but with a remarkable prevalence of atherosclerotic lesions (18.8%) and aortitis (13.7%). Degenerative patients more frequently had bicuspid aortic valve (37.2%; P = .002). Patients in the atherosclerotic group were older (median age, 69 years; P < .001), more often with a history of hypertension (87.5%; P = .059), hypercholesterolemia (75%; P = .019), diabetes (16.6%; P = .054), current smoking (22.9%; P = .066), and a history of coronary artery disease (18.7%; P = .063). Patients with aortitis represented the older group (median age, 75 years, P < .001), were mostly females (68.6%; P < .001), and had a larger ascending aorta diameter (median, 56 mm; P < .001). Both patients with atherosclerosis and aortitis presented a higher incidence of concomitant abdominal aortic aneurysm (20.8% and 22.8%, respectively; P < .001). Conclusions: Although degenerative histopathology is the most frequent substrate in ascending TAA, atherosclerosis and inflammation significantly contribute to the development of chronic aortic thoracic disease.
2020
Leone O., Corsini A., Pacini D., Corti B., Lorenzini M., Laus V., et al. (2020). The complex interplay among atherosclerosis, inflammation, and degeneration in ascending thoracic aortic aneurysms. THE JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 160(6), 1434-1443.e6 [10.1016/j.jtcvs.2019.08.108].
Leone O.; Corsini A.; Pacini D.; Corti B.; Lorenzini M.; Laus V.; Foa A.; Bacchi Reggiani M.L.; Di Marco L.; Rapezzi C.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/739574
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