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Sudden Death Due to Unusual Complication of Takayasu Arteritis: An Autopsy Case
Maher Jedidi1, Youssef Chkirbene, Nihed Abdessayed
1From the Departments of *Legal Medicine, †Pathology, and ‡Hospital Hygiene, Farhat Hached University Hospital, Sousse, Tunisia; and §Department of Legal Medicine, Ibn El jazzar University Hospital, Kairouan, Tunisia.
Abstract:
Takayasu arteritis is an uncommon inflammatory disease with usually a good prognosis. However, sometimes, the evolution can be fatal essentially by a coronary arteries involvement. We present a case of a 19-year-old woman who died suddenly from cardiogenic shock complicating an unknown Takayasu arteritis.At the autopsy, the aorta showed a significant thickening of the wall. The coronary arteries were slightly thickened and did not show any occlusion. Microscopic examination of the aorta showed an abundant granulomatous and a lymphoplasmacytic infiltrate. Microscopic sections of other internal organs showed signs of cardiac hypertrophy and an extensive edema of the lung. Death was attributed to acute heart failure complicating a supravalvular aortic stenosis secondary to unknown Takayasu arteritis.Takayasu arteritis can be life-threatening by an occlusion of the ascending aorta and its major branches, without any coronary arteries involvement.
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