Abstract

Background and aim of the study: Inflammation of the aortic wall may be responsible for the onset of aneurysms and dissections requiring surgical treatment. We evaluate the incidence of aortitis on a selected surgical population searching for any relationship with systemic diseases, verify early and late surgical results and provide clinical and radiological follow-up to determine factors potentially predicting progression and influencing late outcome. Methods: From 2009 to 2017, 237 patients underwent elective operations on the ascending aorta. Segments of the excised tissues were routinely sent for histological evaluation, providing adequate data in 178 (75%) for a clinical and pathological correlation. Patients with aortitis (Group 1) (n = 26) were compared with 152 with atherosclerotic or degenerative disease (Group 2). Results: Incidence of aortitis was 15%, being clinically isolated in 73%. In 24 patients (92%) a giant cell aortitis was found. Actuarial survival at 3 years is 88% in Group 1 and 98% in Group 2 and 74% and 98% at 5 years, respectively (p = 0.016). A control angio-computed tomography revealed an increased descending aorta diameter in 3 out of 14 late survivors. A positron emission tomography showed presence of arteritis in other vascular segments in 3 patients. Conclusions: Clinically isolated aortitis is extremely frequent in patients with inflammatory aortic disease. The diagnosis is often difficult and may be supported by routine pathological evaluation of surgical explants and by multimodality imaging. The latter should be employed to allow adequate patient follow-up and to disclose potential recurrences in untreated aortic segments.

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