CC BY-NC-ND 4.0 · AJP Rep 2019; 09(02): e144-e146
DOI: 10.1055/s-0039-1683936
Case Report
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Pentalogy of Cantrell in Full Term Neonate

Nadereh Taee
1   Department of Pediatrics, Lorestan University of Medical Sciences, Khorramabad, Iran
,
Mojgan Faraji Goodarzi
1   Department of Pediatrics, Lorestan University of Medical Sciences, Khorramabad, Iran
,
Mohammad Safdari
2   Medical Student, Lorestan University of Medical Sciences, Khorramabad, Iran
,
Amir Bajelan
2   Medical Student, Lorestan University of Medical Sciences, Khorramabad, Iran
› Author Affiliations
Further Information

Publication History

26 April 2018

30 December 2018

Publication Date:
09 April 2019 (online)

Abstract

Pentalogy of Cantrell (PC) is an uncommon congenital disorder characterized by severe defects in the chest and abdomen, including abdominal visceral prolapsed via umbilical cord (omphalocele), defect in the lower part of the sternum, defect in the front of the diaphragm, defects in the anterior part of the pericardium, and the ectopiacordis. Here, we report a 2-hour-old girl, weighing 3,500 g, who was referred to Shahid Madani Hospital in Khorramabad due to the large omphalocele on her chest with pulsating mass above it. The baby was the first child of a 24-year-old mother who was born with an uncomplicated vaginal delivery. Very rare cases of PC are born as a term new-born.

Compliance with Ethical Standards

Research involving human participants and/or animals–ethical approval: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.


Informed Consent

Informed consent was obtained from all individual participants included in the study.


 
  • References

  • 1 Carmi R, Boughman JA. Pentalogy of Cantrell and associated midline anomalies: a possible ventral midline developmental field. Am J Med Genet 1992; 42 (01) 90-95
  • 2 Martin RA, Cunniff C, Erickson L, Jones KL. Pentalogy of Cantrell and ectopia cordis, a familial developmental field complex. Am J Med Genet 1992; 42 (06) 839-841
  • 3 Nayak S, Dash SP, Khatua M. Fetal anomaly: Pentalogy of Cantrell. IOSR J Dent. Med Sci 2015; 14 (06) 52-55
  • 4 Puvabanditsin S, Di Stefano V, Garrow E, Wong R, Eng J, Balbin J. Ectopia cordis. Hong Kong Med J 2013; 19 (05) 447-450
  • 5 Chandran S, Ari D. Pentalogy of cantrell: an extremely rare congenital anomaly. J Clin Neonatol 2013; 2 (02) 95-97
  • 6 Parvari R, Weinstein Y, Ehrlich S, Steinitz M, Carmi R. Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25-26. Am J Med Genet 1994; 49 (04) 431-434
  • 7 Vazquez-Jimenez JF, Muehler EG, Daebritz S. , et al. Cantrell's syndrome: a challenge to the surgeon. Ann Thorac Surg 1998; 65 (04) 1178-1185
  • 8 Jafarian AH, Omidi AA, Fazel A, Sadeghian H, Joushan B. Pentalogy of Cantrell: a case report. J Res Med Sci 2011; 16 (01) 105-109
  • 9 Taee N, Tarhani F, Goodarzi MF, Safdari M, Bajelan A. Mermaid syndrome: a case report of a rare congenital anomaly in full-term neonate with thumb deformity. AJP Rep 2018; 8 (04) e328-e331