Prabhu Savit, Sigamani Elanthenral, Das Prasenjit, Sasi Arun, Safaya Rajni
Department of Pathology, All India Institute of Medical Sciences, New Delhi 110029, India.
BMJ Case Rep. 2009;2009:bcr0120091518. doi: 10.1136/bcr.01.2009.1518. Epub 2009 Apr 1.
Potter syndrome is a congenital anomaly characterised by bilateral renal agenesis, pulmonary hypoplasia, cardiac, skeletal abnormalities and maternal oligohydramnios. Here we report a case of Potter syndrome with bilateral renal agenesis, pulmonary hypoplasia and complete transposition of the great vessels, which had been identified during a post-mortem examination. Although cardiac anomalies are known to exist with Potter syndrome, complete transposition of the great vessels has not been reported in the literature.
波特综合征是一种先天性异常,其特征为双侧肾缺如、肺发育不全、心脏和骨骼异常以及母体羊水过少。在此,我们报告一例波特综合征病例,该病例伴有双侧肾缺如、肺发育不全和大动脉完全转位,这是在尸检过程中发现的。虽然已知波特综合征存在心脏异常,但大动脉完全转位在文献中尚未见报道。