Case Report Open Access
Copyright ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Nov 6, 2020; 8(21): 5389-5393
Published online Nov 6, 2020. doi: 10.12998/wjcc.v8.i21.5389
Early ultrasound diagnosis of conjoined twins at eight weeks of pregnancy: A case report
Xiao-Wen Liang, Yao-Zhang Yang, Zhi-Yi Chen, Department of Ultrasound Medicine, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou 510000, Guangdong Province, China
Yong-Yi Cai, Department of Ultrasound, Liwan Hospital of the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou 510000, Guangdong Province, China
ORCID number: Xiao-Wen Liang (0000-0002-9797-798X); Yong-Yi Cai (0000-0002-1212-3476); Yao-Zhang Yang (0000-0001-8528-2366); Zhi-Yi Chen (0000-0002-5973-4522).
Author contributions: Liang XW was responsible for substantial contributions to conception and design; Cai YY was responsible for the acquisition of data; Yang YZ was responsible for drafting the article; Chen ZY was responsible for the final approval of the version to be published.
Supported by Major Research Projects of Universities in Guangdong Province, No. 2019KZDZX1032; the Open Laboratory Project of Guangzhou Medical University in 2019, No. C195015026; Youth Foundation of Scientific Research of the Third Affiliated Hospital of Guangzhou Medical University, No. 2018Q18.
Informed consent statement: All study participants, or their legal guardian, provided informed written consent prior to study enrollment.
Conflict-of-interest statement: The authors have no conflicts of interest.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Zhi-Yi Chen, PhD, Professor, Department of Ultrasound Medicine, The Third Affiliated Hospital of Guangzhou Medical University, No. 63 Duobao Road, Guangzhou 510000, Guangdong Province, China. zhiyi_chen@gzhmu.edu.cn
Received: April 21, 2020
Peer-review started: April 29, 2020
First decision: September 12, 2020
Revised: September 13, 2020
Accepted: September 23, 2020
Article in press: September 23, 2020
Published online: November 6, 2020
Processing time: 191 Days and 2.4 Hours

Abstract
BACKGROUND

Conjoined twins are a rare occurrence, and the majority of these malformations are detected during second trimester screening.

CASE SUMMARY

Herein we report a case of conjoined twins, which was diagnosed by ultrasound at 8 wk gestation and was normal at 7 wk gestation. The two fetuses shared one heart and were diagnosed as thoracopagus twins. This is the first report of conjoined twins diagnosed at 8 wk gestation. The pregnancy was terminated electively at 9 wk gestation. Because some congenital malformations can be diagnosed earlier, a prenatal ultrasound examination at an early gestational stage cannot be dismissed.

CONCLUSION

This case demonstrates that a 7-8 wk gestation might be the earliest period when conjoined twins can be diagnosed by ultrasound.

Key Words: Conjoined twins; Ultrasound; Thoracopagus; Early diagnosis; Congenital malformation; Case report

Core Tip: A woman at 8 wk of pregnancy with low progesterone levels came to the hospital for a routine ultrasound examination. Ultrasound showed a twin pregnancy, and the two fetuses were conjoined by the chest and heart. However, the ultrasound performance showed a normal singleton pregnancy at her 7th wk of pregnancy. We found that ultrasound examination at 7-8 wk of pregnancy plays an important role in the early diagnosis of congenital malformation in twins.



INTRODUCTION

Conjoined twins are extremely rare fetal abnormalities with a reported prevalence of 1:50000-1:100000[1]. Conjoined twins result from postzygotic splitting 13 d after fertilization[2]. Approximately 70% of conjoined twins die within 24-48 h after birth or have a fatal congenital disease; thus, early diagnosis and treatment are desirable[3]. In a previous study, conjoined twins were diagnosed by ultrasound between 18 and 22 wk gestation[4]. More recent research has reported the diagnosis of fetal defects in twin pregnancies at 11-13 wk gestation[5]. Termination of pregnancy as early as possible continues to be the best treatment. Herein we report a case of conjoined twins suspected of cardiac fusion diagnosed by prenatal ultrasound at 8 wk gestation and confirmed by surgery.

CASE PRESENTATION
Chief complaints

At 8 wk gestation, a pregnant woman presented with low progesterone level.

History of present illness

A 30-year-old woman had a normal prenatal ultrasound examination at 7 wk gestation. The patient did not have any other discomfort.

History of past illness

The patient is G4P1. She delivered her first child vaginally.

Personal and family history

The patient has no special family history.

Physical examination

The patient’s physical examination was normal.

Laboratory examinations

Laboratory testing had revealed a low progesterone level.

Imaging examinations

The first prenatal transvaginal ultrasound was performed by CD-6 (Mindray, Shenzhen, China) at 7 wk gestation. Two-dimensional ultrasound images showed that the embryo was normal with crown-rump length of 12 mm (Figure 1).

Figure 1
Figure 1 Ultrasound imaging of the embryo at seven weeks gestation.

After 7 d, the prenatal ultrasound was performed again using a Volusion E8 (GE Healthcare, Milwaukee, WI, United States). Two-dimensional ultrasound images showed a single yolk and two embryos in the gestational sac. The lengths of the two embryos were 18 mm and 20 mm. The embryos were connected without distinct boundaries, and there was no fluid between them. The two embryos shared one heart. Color Doppler flow imaging showed that pulsating blood flow signals existed at the junction of the two embryos (Figure 2).

Figure 2
Figure 2 Ultrasound imaging of the embryo at eight weeks gestation. A: Two embryos and two spines can be seen in the long axial view; B: Two brains can be seen in the short axial view; C: Two gastric vacuoles and two bladders can be seen; D: Color Doppler flow imaging showed that the two embryos had only one beating heart.
FINAL DIAGNOSIS

Conjoined twins (thoracopagus twins).

TREATMENT

Terminated the pregnancy through abortion.

OUTCOME AND FOLLOW-UP

Discharge after a period of observation.

DISCUSSION

Conjoined twins are very rare monozygotic variants, most of which are monochorionic monoamniotic twins[6]. Although the basis of conjoined twins has not been established, there are two main theories. The first theory is that incomplete division of an early embryo produces identical twins with the same anatomic structures. The other theory is that conjoined twins are the result of two separate embryos reuniting again.

Conjoined twins are classified based on the conjoined body parts. The most common type of conjoined twins is an abdominal union, which accounts for 87% with a mortality rate of 51%, while dorsal unions occur in up to 13% of conjoined twins[7,8]. Cardiac fusion usually occurs in thoracopagus twins, but rarely occurs in ischiopagus, craniopagus, or pygopagus twins. Along with the improvements in surgical technique, survival rates for separation procedures have increased. Although cardiac fusion is relatively common in conjoined twins, the success rate of surgical separation and diagnostic accuracy for this type is extremely low.

In most cases of conjoined twins, a severely deformed connection is fatal for the surviving fetus[9]. However, severe malformations are always caused by the untimely diagnosis, which delays optimal surgical treatment. Chen et al[10] studied the outcomes of postnatal surgical separation of conjoined twins diagnosed before 15 wk gestation. The survival rate of emergency surgery (10%-29%) was reported to be much lower than nonemergent, planned surgery (81%-83%). Recently, Heuer et al[11] successfully separated total-fusion craniopagus twins at 10 mo of age. Dunaway[12] concluded that there are many unknowns regarding the research of separating craniopagus twins in stages. Moreover, in couples who opt to continue the pregnancy, a multidisciplinary team for prenatal and postnatal management is necessary because multiple malformations are often found[13].

It was also demonstrated that early diagnosis of conjoined twins is necessary. Early diagnosis of conjoined twins has the following advantages. First, through the early evaluation of the degree of fusion, the optimal treatment time and strategy can be selected. In addition, early diagnosis will minimize maternal and fetal mortality. Early evaluation will also help parents to choose early termination, thereby reducing the risk of trauma during vaginal delivery[14].

CONCLUSION

In conclusion, the incidence of conjoined twins is low, but the rate of mortality and malformations (such as severe congenital lung disease) is high. Termination of pregnancy may be a wise choice, especially when the vital organs of the body are connected. This study suggests that active and regular antenatal ultrasonic examinations provide a great opportunity for good prognosis. Interdisciplinary integration also plays an important role in the diagnosis and treatment of conjoined twins[15]. We suppose that an ultrasound examination at 7-8 wk of pregnancy plays an important role in the early diagnosis of congenital malformations in twins. Therefore, apart from the heartbeat and calculation of gestational age, sonographers should also notice the fetal structure in early examinations.

Footnotes

Manuscript source: Unsolicited manuscript

Specialty type: Medicine, research and experimental

Country/Territory of origin: China

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P-Reviewer: Ciccone MM S-Editor: Zhang L L-Editor: Filipodia P-Editor: Wang LL

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