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川崎病所致主动脉瓣反流的主动脉瓣置换术。两例报告。

Aortic valve replacement for aortic regurgitation due to Kawasaki disease. Report of two cases.

作者信息

Fukunaga S, Egashira A, Arinaga K, Akasu I, Kai E, Higashi T, Kosuga K, Aoyagi S, Kazue T

机构信息

Second Department of Surgery, Kurume University School of Medicine, Japan.

出版信息

J Heart Valve Dis. 1996 Mar;5(2):231-4.

PMID:8665019
Abstract

Two cases of severe aortic regurgitation due to Kawasaki disease are reported. Both patients were diagnosed as having Kawasaki disease in their infancy, and were followed up by a pediatrician. Aortic regurgitation was detected 18 months in one case and 36 days in the other case after onset of the illness. With the passage of time, the aortic regurgitation increased and aortic valve replacement was scheduled in both patient at the age of 13. On admission, two-dimensional echocardiography showed thickening of the aortic cusps, and severe aortic regurgitation was detected by color flow Doppler studies. Successful aortic valve replacement was performed, and histological studies of the cusps showed sequelae of valvulitis. In conclusion, aortic regurgitation is a rare complication of Kawasaki disease, and the aortic valve function, especially occurrence of aortic regurgitation, should be carefully observed in patients with a past history of Kawasaki disease.

摘要

报告了两例川崎病所致的严重主动脉瓣反流病例。两名患者均在婴儿期被诊断为川崎病,并由儿科医生进行随访。发病后18个月,其中1例检测到主动脉瓣反流;另1例在发病后36天检测到主动脉瓣反流。随着时间的推移,主动脉瓣反流加重,两名患者均计划在13岁时进行主动脉瓣置换术。入院时,二维超声心动图显示主动脉瓣叶增厚,彩色多普勒血流显像检查发现严重主动脉瓣反流。成功实施了主动脉瓣置换术,瓣叶组织学检查显示存在瓣膜炎后遗症。总之,主动脉瓣反流是川崎病的一种罕见并发症,对于有川崎病病史的患者,应仔细观察其主动脉瓣功能,尤其是主动脉瓣反流的发生情况。

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