Mohan J C, Tatke M, Arora R
Department of Cardiology, G.B. Pant Hospital, New Delhi, India.
Int J Cardiol. 1989 Oct;25(1):136-9. doi: 10.1016/0167-5273(89)90177-0.
Tricuspid regurgitation due to rudimentary and dysplastic tricuspid valvar tissue associated with a patent right ventricular outflow tract is described in a 10-year-old child presenting with cyanosis since birth. The diagnosis was confirmed by cross-sectional echocardiography, angiocardiography and subsequently by histopathological data. We discuss the differentiation of these findings from Uhl's anomaly and from the congenitally unguarded tricuspid orifice.
本文描述了一名自出生以来即有发绀症状的10岁儿童，其因发育不全且发育异常的三尖瓣组织伴右心室流出道通畅而导致三尖瓣反流。通过横断面超声心动图、心血管造影以及随后的组织病理学数据确诊。我们讨论了这些发现与乌尔氏畸形以及先天性三尖瓣无保护口的鉴别。
