Cantrell pentalojisi

Year 2015, Volume: 25 Issue: 3, 95 - 97, 01.09.2015

Tuncay Yüce Seda Şahin Aker Erkan Kalafat F. Acar Koç

Abstract

Cantrel pentalojisi nadir görülen bir sendromdur. Gelişen teknoloji ile birlikte son yıllarda erken haftalarda tanı konabilmektedir. Tanı konulan hastalarda gebeliğin sonlandırılması önerilmekte ve bir çok hastada terminasyon uygulanmaktadır. Ancak nadiren de olsa aile terminasyon seçeneğini kabul etmediğinden dolayı terme ulaşan fetuslar görülmektedir. Bizim vakamız da terme kadar ulaşan ve doğum esnasında kaybedilen bir Cantrel pentalojisi vakasıdır

Keywords

Cantrel pentalojisi, prenatal tanı, ektopia kordis

Cantrell pentalogy

Abstract

Pentalogy of Cantrell is a rare congenital malformation. The condition is usually diagnosed prenatally with ultrasound and families are informed about prognosis. Although many families opt for termination of pregnancies, there are cases of live births. We present a case of Pentalogy of Cantrell, delivered with cesarean section at full term

Keywords

Cantrell pentalogy, prenatal diagnosis, ectopia cordis

References

• Cantrell JR, Haller JA, Ravitch MM. A syndrome of congenital de- fects involving the abdominal wall, sternum, diaphragm, pericardi- um and heart. Surg Gynecol Obstet 1958;107:602-14.
• Desselle C, Herve P, Toutain A, et al. Pentalogy of Cantrell: sonog- raphic assessment. J Clin Ultrasound 2007;35:216-20.
• Ghidini A, Sirtori M, Romero R, Hobbins JC. Prenatal diagnosis of pentalogy of Cantrell. J Ultrasound Med 1988;7:567-72.
• Carmi R, Boughman JA. Pentalogy of Cantrell and associated mid- line anomalies: a possible ventral midline developmental field. Am J Med Genet 1992;42:90-5.
• Toyama WM. Combined congenital defects of the anterior abdo- minal wall, sternum, diaphragm, pericardium, and heart: a case report and review of the syndrome. Pediatrics 1972;50:778-92.
• Parvari R, Carmi R, Weissenbach J, et al. Refined genetic map- ping of X-linked thoracoabdominal syndrome. Am J Med Genet 1996;61:401-2.
• Varras M, Anastasiadis A, Akrivis C, Gialelis J. Pentalogy of Cant- rell in the human foetuses: A rare congenital malformation. OA Case Reports 2013;15:143.
• Steiner MB, Vengoechea J, Collins RT, 2nd. Duplication of the ALDH1A2 gene in association with pentalogy of Cantrell: a case report. J Med Case Rep 2013;7:287.
• Yang TY, Tsai PY, Cheng YC, Chang FM, Chang CH. Prenatal diag- nosis of pentalogy of Cantrell using three-dimensional ultrasound. Taiwan J Obstet Gynecol 2013;52:131-2.
• Vazquez-Jimenez JF, Muehler EG, Daebritz S, et al. Cantrell’s synd- rome: a challenge to the surgeon. Ann Thorac Surg 1998;65:1178- 85.
• Jagtap SV, Shukla DB, Jain A, Jagtap SS. Complete Pentalogy of Cantrell (POC) with phocomelia and other associated rare anoma- lies. J Clin Diagn Res 2014;8:FD04-5.
• Bittmann S, Ulus H, Springer A. Combined pentalogy of Cantrell with tetralogy of Fallot, gallbladder agenesis, and polysplenia: a case report. J Pediatr Surg 2004;39:107-9
• O’Gorman CS, Tortoriello TA, McMahon CJ. Outcome of children with Pentalogy of Cantrell following cardiac surgery. Pediatr Car- diol 2009;30:426-30.
• Turkcapar AF, Sargin Oruc A, Oksuzoglu A, Danisman N. Diag- nosis of pentalogy of cantrell in the first trimester using transva- ginal sonography and color Doppler. Case Rep Obstet Gynecol 2015;2015:179298.
• Yang TY, Tsai PY, Cheng YC, Chang FM, Chang CH. Prenatal diag- nosis of pentalogy of Cantrell using three-dimensional ultrasound. Taiwan J Obstet Gynecol 2013;52:131-2.