An autopsy case of aortic dissection due to giant cell arteritis

被引:0
|
作者
Sakashita, Mai [1 ]
Sakashita, Shingo [2 ]
Uesugi, Noriko [3 ]
Tokunaga, Chiho [4 ]
Hiramatsu, Yuji [4 ]
Noguchi, Masayuki [5 ]
Sakamoto, Noriaki [5 ]
机构
[1] Tsuchiura Kyodo Gen Hosp, Dept Pathol, Ibaraki, Japan
[2] Natl Canc Ctr, Div Pathol, Exploratory Oncol Res & Clin Trial Ctr, Chiba, Japan
[3] Fukuoka Univ, Dept Pathol, Fukuoka, Japan
[4] Univ Tsukuba, Dept Cardiovasc Surg, Fac Med, Ibaraki, Japan
[5] Univ Tsukuba, Dept Diagnost Pathol, Fac Med, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan
关键词
abdominal aortic aneurysm; aortic dissection; EVAR; giant cell arteritis; large-vessel vasculitis;
D O I
10.1111/pin.13046
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Giant cell arteritis (GCA) is a systemic vasculitis affecting mainly large and medium-sized arteries. GCA sometimes involves the aorta and its major branches and causes aortic dissection as a rare complication. We have experienced an autopsy case of aortic dissection due to GCA. The patient was an 87-year-old Japanese woman with Stanford type A aortic dissection who died 7 days after admission. Two years previously she had been diagnosed as having abdominal aortic aneurysm and undergone endovascular aneurysm repair (EVAR). Although she had no characteristic symptoms of GCA, autopsy revealed marked granulomatous inflammation in the dissected area and coronary arteries. Active arteritis was evident not only in the arteries of the upper extremity but also those in the lower extremity. Granulomatous inflammation was not evident in the aneurysm. The aortic dissection might have been an initial manifestation of GCA. We report the regions of GCA extension and its histology in detail.
引用
收藏
页码:204 / 209
页数:6
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