青少年型赖特综合征中的主动脉瓣关闭不全。
Aortic insufficiency in Reiter's syndrome of juvenile onset.
作者信息
Hübscher O, Graci y Susini J
出版信息
J Rheumatol. 1984 Feb;11(1):94-5.
PMID:6607995
Abstract
Reiter's syndrome is an uncommon cause of childhood arthritis and aortic incompetence is extremely rare in these patients. A 7-year-old boy with Reiter's syndrome and hemodynamically significant aortic insufficiency is reported. He was HLD-B27 positive and valvular incompetence was detected 32 months after the onset while active synovitis was still present.
摘要
赖特综合征是儿童关节炎的一种罕见病因，主动脉瓣关闭不全在这些患者中极为罕见。本文报道了一名患有赖特综合征且存在血流动力学显著意义的主动脉瓣关闭不全的7岁男孩。他HLD-B27呈阳性，在发病32个月后检测到瓣膜关闭不全，此时仍存在活动性滑膜炎。
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