Charles Adrian, Dickinson Jan E, Watson Susan, Phillips Nevile, Yovich John
Department of Pathology, King Edward Memorial Hospital, Bagot Road, Subiaco, WA 6008, Australia.
Pediatr Dev Pathol. 2005 Nov-Dec;8(6):666-72. doi: 10.1007/s10024-005-0009-8. Epub 2005 Oct 5.
We present a case of triplets, 2 of whom were monochorionic diamniotic conjoined fetuses, and the other triplet was in a separate chorion. The pregnancy followed in vitro fertilization with 2 embryo transfers and the conjoined fetuses developed from a single embryo. An early ultrasound showed 2 embryos attached to 1 yolk sac. Further monitoring of the pregnancy showed these 2 triplets to be diamniotic with a short umbilical cord/body stalk anomaly. After fetal loss a postmortem examination demonstrated that these fetuses were conjoined with a body stalk anomaly/short umbilical cord syndrome with fusion of the coelomic cavities and small bowel (minimally united/conjoined twins). There were dividing amniotic membranes. This case demonstrates the development of an unusual type of conjoined twin with characteristic features. Conjoined fetuses with this pattern have fused small bowel and cloacal anomalies and often diamniotic placentation, when this is recorded. Various terms including minimally united/conjoined omphalopagus/ischiopagus have been used for this characteristic pattern, but this pattern may warrant a specific term. "Diamniotic vitellopagus" may best reflect the pathogenesis of this pattern.
我们报告一例三胞胎病例,其中2个为单绒毛膜双羊膜囊联体胎儿,另一个三胞胎位于单独的绒毛膜内。该妊娠是在进行2次胚胎移植的体外受精后发生的,联体胎儿由单个胚胎发育而来。早期超声检查显示2个胚胎附着于1个卵黄囊。对该妊娠的进一步监测显示,这2个三胞胎为双羊膜囊,伴有短脐带/体蒂异常。胎儿丢失后进行的尸检表明,这些胎儿联体,伴有体蒂异常/短脐带综合征,体腔和小肠融合(轻度联合/联体双胎)。有分隔的羊膜。该病例展示了一种具有特征性的不寻常类型联体双胎的发育情况。具有这种模式的联体胎儿有融合的小肠和泄殖腔异常,且在有记录时通常为双羊膜胎盘。包括轻度联合/联体胸腹联体/坐骨联体在内的各种术语已被用于描述这种特征性模式,但这种模式可能需要一个特定的术语。“双羊膜卵黄联体”可能最能反映这种模式的发病机制。