Three-dimensional ultrasonographic features of diamniotic conjoined twins with body stalk anomaly

• Main Authors: Guishuang Xiang (Author), Yanting Wen (Author), Li Zhang (Author), Xiaoqian Tong (Author), Lu Li (Author)
• Format: Book
• Published: BMC, 2020-04-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.
• Notes: 10.1186/s12884-020-02920-0; 1471-2393
• Keywords: Conjoined twins; Monochorionic-diamniotic; Ultrasound; Yolk sac; Body stalk anomaly; Gynecology and obstetrics; RG1-991
• Source: BMC Pregnancy and Childbirth, Vol 20, Iss 1, Pp 1-5 (2020)

Abstract Background Since conjoined twins were thought to be monoamniotic in the past, diamniotic conjoined twins would be improbable theoretically. Body stalk anomaly is a severe defect of the body wall, which is rare among twins. Body stalk anomaly in monochorionic diamniotic conjoined twins has never been reported prenatally so far as we know. Case presentation Here we present an extremely rare case of concordant body stalk anomaly in monochorionic diamniotic conjoined twins. Ultrasonography at 9 + 5 weeks revealed one chorionic and two amniotic cavities, close apposition of abdomen, limited movement, and common umbilical vessels. Follow-up ultrasonography at 11 + 6 weeks and 13 + 2 weeks showed close apposition of the lower abdominal region with cystic structures and a small bowel-like mass between the two fetuses. Three-dimensional ultrasonography assisted in observing the entire appearance of both twins in earlier first trimester, including amnioticity, conjoined region and umbilical vessels. We attribute this diamniotic conjoined twin in our case to the fusion theory. A single yolk sac was observed, challenging the idea that yolk sac number predicts amnionicity. Identification of single yolk sac and its allantois may form a common body stalk during this fusion, leading to concordant body stalk anomaly in monochorionic diamniotic twins. Conclusions Our case may provide important insights into both ultrasonographic features and embryogenesis of this extremely rare anomaly.