Prenatal diagnosis of Meckel’s diverticulum in a foetus


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

Background. Meckel’s diverticulum (MD) is a remnant of the vitelline duct of the foetus and develops in the sixth week of embryogenesis. It is present in 2-3% of population and remains the most common anomaly of the digestive tract. There are only a few conf irmed cases detected prenatally. Description. We present a case study of a pregnant woman where from the 17 weeks’ pregnancy an anechoic area in the fetal abdomen was observed. During a routine ultrasound examination, a round cyst measuring 11.9 x 8.1 mm, with hyperechogenic thick walls was found just below the liver. In check- up scans conducted every three weeks, no progression was discovered. Conclusion. Our case is the only one in the literature documented so well by prenatal scans preformed every 3 weeks and followed up for three years from detection. Meckel’s diverticulum should be an element of differential diagnostics of intra-abdominal anechoic areas in a foetus.

全文:

受限制的访问

作者简介

Arkadiusz Krzyzanowski

The Medical University of Lublin

Email: a_r_krzyzanowski@tlen.pl
MD, PhD, Department of Obstetrics and Pathology of Pregnancy

Adrianna Kondracka

The Medical University of Lublin

Email: adriannakondracka@wp.pl
MD, PhD, Department of Obstetrics and Pathology of Pregnancy

Aleksandra Stupak

The Medical University of Lublin. Poland

Email: aleksandra.stupak@umlub.pl
MD, PhD, Department of Obstetrics and Pathology of Pregnancy

Anna Kwasniewska

The Medical University of Lublin

Email: anna.kwasniewska@umlub.pl
MD, Prof., PhD, Department of Obstetrics and Pathology of Pregnancy

参考

  1. Lüdtke F.E., Mende V., Köhler H., Lepsien G. Incidence and frequency of complications and management of Meckel’s diverticulum. Surg. Gynecol. Obstet. 1989; 169(6): 537-42.
  2. Komuro H., Hoshino N., Urita Y., Fujishiro J., Sakamoto N., Ono K., Kaneko M. Pathogenic implications of remnant vitelline structures in gastroschisis. J. Pediatr. Surg. 2010; 45(10): 2025-9.
  3. Stevenson R.E., Rogers R.C., Chandler J.C., Gauderer M.W., Hunter A.G. Escape of the yolk sac: a hypothesis to explain the embryogenesis of gastroschisis. Clin. Genet. 2009; 75(4): 326-33.
  4. Lin C.H., Wu S.F., Lin W.C., Chen A.C. Meckel’s diverticulum induced intrauterine intussusceptions associated with ileal atresia complicated by meconium peritonitis. J. Formos. Med. Assoc. 2007; 106(6): 495-8.
  5. Synder Ch.L. Meckel’s diverticulum. In: Ashcroft K., ed. Pediatric surgery. Saunders Company; 2001.
  6. Delle Chaiaie L., Neubergert P. Early prenatal sonographic dection of an uncomplicated Meckel diverticulum. Ultrasound Obstet. Gynecol. 2007; 30(5): 790-1.
  7. Rogula S., Lepiarczyk A., Porebska A., Malarewicz A. Rare case of innate obstruction of digestive tract diagnosed by USG examination of fetus in the 30th week of pregnancy. Ginecol. Pol. 2001; 72(9): 773-7.
  8. Pavlovic S., Zdravkovic D., Stefanovic N., Pavlovic M., Bakic M., Zivkovic V. Anatomohistological characteristics of Meckel’s diverticulum in human fetuses. Vojnosanit. Pregl. 2008; 65(8): 606-11.
  9. Rushford M.P., Stys S.J., Latchaw L.A., Kasales C., Vaccaro T. Prenatal sonographic detection of Meckel diverticulum in utero with postnatal radiologic and surgical confirmation. J. Ultrasound Med. 2004 23(2): 319-21.
  10. Borgi A., Bouziri A., Boujelbene N., Sghairoun N., Belhadj S., Benjeballah N. Perforated Meckel’s diverticulum in a very preterm baby revealed at birth. Fetal Pediatr. Pathol. 2014; 33(2): 119-22.

补充文件

附件文件
动作
1. JATS XML

版权所有 © Bionika Media, 2017
##common.cookie##