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胚胎期小鼠头胸联体双胎病例。

Case of cephalothoracopagus conjoined twinning in an embryonic mouse.

作者信息

Hynd Thomas E, Buckley Cadie L, Lozanoff Scott

机构信息

Department of Anatomy, Biochemistry and Physiology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI 96813, USA.

出版信息

Birth Defects Res A Clin Mol Teratol. 2013 Jun;97(6):421-4. doi: 10.1002/bdra.23151. Epub 2013 Jun 13.

Abstract

BACKGROUND

Cephalothoracopagus twinning is extremely rare, and it is characterized by fusion of the head and thorax, two separate spines, pelves, and fore- and hindlimbs.

CASE

In this case study, we describe cephalothoracopagus twinning in an embryonic mouse displaying a large but exencephalic head, median facial cleft, a single eye, and a second hindbrain rotated roughly 90° from a second spinal cord. There is a bony connection joining the clavicles, resulting in merged asternal thoracic cavities containing two hearts and four lungs. The abdominal cavities contain double caudal digestive tract structures, but a single esophagus and stomach.

CONCLUSION

There are several proposed theories regarding the mechanism of spontaneous conjoined twinning; however, the specific mechanisms are still largely unknown. In this report, we highlight the morphological features in a murine example of cephalothoracopagus twinning, furthering our understanding of this rare occurrence while also demonstrating developmental morphogenesis consistent with that reported for human conjoined twins.

摘要

背景

头胸联体双胎极为罕见,其特征为头部与胸部融合,有两根独立的脊柱、骨盆以及前肢和后肢。

病例

在本病例研究中,我们描述了一只胚胎小鼠的头胸联体双胎情况,该小鼠头部较大但无脑,面部正中裂,单眼,且第二个后脑相对于第二根脊髓大致旋转了90°。有一个骨性连接连接着锁骨,导致合并的无胸骨胸腔内有两颗心脏和四个肺。腹腔内有双尾消化道结构,但食管和胃为单个。

结论

关于自然联体双胎的机制有几种提出的理论;然而,具体机制在很大程度上仍然未知。在本报告中,我们突出了头胸联体双胎小鼠实例中的形态学特征,增进了我们对这种罕见情况的理解,同时也展示了与人类联体双胎报道一致的发育形态发生过程。

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