Sennari E, Nishiguchi T, Okishima T, Koono M, Matsuoka Y, Sato Y, Hayakawa K
Department of Pediatrics, Miyazaki Medical College, Japan.
Pediatr Cardiol. 1990 Jan;11(1):50-3. doi: 10.1007/BF02239549.
The case of a female neonate with truncus solitarius pulmonalis (TSP), a rare congenital heart anomaly, is reported. She died four days after birth. A single right ventricle with common atrioventricular (AV) valve was associated with (Collet & Edwards type II) truncus arteriosus communis, and appeared to have a single coronary artery with an abnormally high take-off near the origin of the right subclavian artery. However, the vessel that appeared to be the single coronary artery was in fact an extremely hypoplastic ascending aorta associated with aortic atresia and agenesis of the left ventricle and mitral valve.
报道了一例患有罕见先天性心脏异常——肺动脉干单一（TSP）的女性新生儿病例。她出生后四天死亡。一个具有共同房室（AV）瓣的单一右心室与（科莱 & 爱德华兹II型）共同动脉干相关联，并且似乎有一条单一冠状动脉，其在右锁骨下动脉起始处附近有异常高位的起始。然而，看似单一冠状动脉的血管实际上是一个极度发育不全的升主动脉，伴有主动脉闭锁以及左心室和二尖瓣发育不全。
