Arai H, Harada K, Tamura M, Okamura T, Takada G
Department of Pediatrics, Akita University School of Medicine, Japan.
Tohoku J Exp Med. 1995 Oct;177(2):171-7. doi: 10.1620/tjem.177.171.
A case of an infant with a rare combination of polysplenia syndrome with common atrioventricular canal and persistent truncus arteriosus is presented. In our present case, severe common atrioventricular valve regurgitation was identified, as in previous cases. To our knowledge, echocardiographic and autopsy findings of this association has not been previously reported. The persistent truncus arteriosus is extremely rare in the setting of the polysplenia syndrome, but the present case report demonstrates that these anomalies may, at times, occur.
本文报告了一例患有多脾综合征、共同房室通道和永存动脉干罕见组合的婴儿病例。在我们目前的病例中,与之前的病例一样,发现了严重的共同房室瓣反流。据我们所知,此前尚未报道过这种关联的超声心动图和尸检结果。永存动脉干在多脾综合征中极为罕见,但本病例报告表明,这些异常情况有时可能会发生。