Journals / Balıkesir Sağlık Bilimleri Dergisi / 2026 / Volume: 12 Issue: 2

Incomplete Cantrell Pentalogy Diagnosis Case Report

İnkomplet Cantrell Pentolojisi Tanı Olgu Sunumu

Mahmut Serkan Sarıkaya(BALIKESİR ÜNİVERSİTESİ TIP FAKÜLTESİ KADIN HASTALIKLARI VE DOĞUM)0000-0003-3464-8246
İpek Dokurel(BALIKESİR ATATÜRK ŞEHİR HASTANESİ)0000-0002-1820-8980
Orkun Çetin(BALIKESİR ÜNİVERSİTESİ, TIP FAKÜLTESİ)0000-0002-9125-2742
Tümerkan Cenk(BALIKESİR ÜNİVERSİTESİ, TIP FAKÜLTESİ)0000-0003-0721-2279
Pages
—
Publication Date
2023-06-23
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In our case we want to evaluate clinical and post clinical pathways insight of literature.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Cantrell pentalogy is a rare disorder encountered in fetal an intrauterine life.
📊
Key Findings & Data:Pentalogy of Cantrell consist more than one pathological components these are sternal, pericardial, diafragmatic, anterior abdominal wall defects.Pentalogy of Cantrell firstly described by Cantrelll and colleageus at 1958.
💡
Conclusion & Impact:In our case we want to evaluate clinical and post clinical pathways insight of literature.
🔬Design:Case Report
📍Scope:Comprehensive Sample
⚙️Variables:Cantrell · incomplete · prognosis

Abstract

Cantrell pentalogy is a rare disorder encountered in fetal an intrauterine life. Pentalogy of Cantrell consist more than one pathological components these are sternal, pericardial, diafragmatic, anterior abdominal wall defects.Pentalogy of Cantrell firstly described by Cantrelll and colleageus at 1958. Prevalance of Cantrell is 1/65.000- 1/200.000. In our case we want to evaluate clinical and post clinical pathways insight of literature.

Özet

Cantrell Pentalojisi, intrauterin ve fetal hayatta karşılaşılan birden fazla doğumsal defektin yer aldığı nadir bir konjenital hastalıktır. Pentalojinin içinde sternal, perikardiyal ,diafragmatik ,kardiyak ve karın ön duvarı patolojileri bulunmaktadır. Cantrell pentalojisinin prevelansı 1/65.000-1/200.000 arasında olup 1958 yılında Cantrell ve arkadaşları tarafından tanımlanmıştır. Olgumuzda birinci trimesterde prenatal tanısı konulan Cantrell pentalojisi olgusunu literatür bilgileri ile beraber tanı ve sonrası için yapılanları değerlendirdik.

🔖

Cite This Article

Sarıkaya, M. S., Dokurel, İ., Çetin, O., Cenk, T. (2023). Incomplete Cantrell Pentalogy Diagnosis Case Report. Balıkesir Sağlık Bilimleri Dergisi, Volume: 12 Issue: 2. https://doi.org/10.53424/balikesirsbd.1055769

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (13)

  1. Cantrell, J. R., Haller, J. A., & Ravitch, M. M. (1958). A syndrome of congenital defects involving the abdominal wall, sternum, diaphragm, pericardium, and heart. Surg Gynecol Obstet, 107(5), 602-614. https://doi.org/10.1259/0007-1285-48-565-52
  2. Toyama, W. M. (1972). Combined congenital defects of the anterior abdominal wall, sternum, diaphragm, pericardium, and heart: a case report and review of the syndrome. Pediatrics, 50(5), 778-792. https://doi.org/10.1542/peds.50.5.778
  3. Mallula, K. K., Sosnowski, C., & Awad, S. (2013). Spectrum of Cantrell’s pentalogy: case series from a single tertiary care center and review of the literature. Pediatric cardiology, 34(7), 1703-1710. https://doi.org/10.1007/s00246-013-0706-4
  4. Cakiroglu, Y., Doger, E., Yildirim Kopuk, S., Babaoglu, K., Caliskan, E., & Yucesoy, G. (2014). Prenatal diagnosis of Cantrell’s pentalogy associated with agenesis of left limb in a twin pregnancy. Case reports in obstetrics and gynecology, 2014. https://doi.org/10.1155/2014/314284
  5. Carmi, R., & Boughman, J. A. (1992). Pentalogy of Cantrell and associated midline anomalies: a possible ventral midline developmental field. American journal of medical genetics, 42(1), 90-95. https://doi.org/10.1002/ajmg.1320420118
  6. Pivnick, E. K., Kaufman, R. A., Velagaleti, G. V. N., Gunther, W. M., & Abramovici, D. (1998). Infant with midline thoracoabdominal schisis and limb defects. Teratology, 58(5), 205-208. https://doi.org/10.1002/(SICI)1096-9926(199811)58:5 3.0.CO;2-X
  7. Uygur, D., Ks, S., Sener, E., Günçe, S., & Semerci, N. (2004). An infant with pentalogy of Cantrell and limb defects diagnosed prenatally. Clinical dysmorphology, 13(1), 57-58.
  8. Correa-Rivas, M. S., Matos-Llovet, I., & García-Fragoso, L. (2004). Pentalogy of Cantrell: a case report with pathologic findings. Pediatric and Developmental Pathology, 7(6), 649-652. https://doi.org/10.1007/s10024-004-9104-5
  9. Morales, J. M., Patel, S. G., Duff, J. A., Villareal, R. L., & Simpson, J. W. (2000). Ectopia cordis and other midline defects. The Annals of thoracic surgery, 70(1), 111-114. https://doi.org/10.1016/S0003-4975(00)01388-6
  10. Polat, I., Gül, A., Aslan, H., Cebeci, A., Ozseker, B., Caglar, B., & Ceylan, Y. (2005). Prenatal diagnosis of pentalogy of Cantrell in three cases, two with craniorachischisis. Journal of Clinical Ultrasound, 33(6), 308-311. https://doi.org/10.1002/jcu.20134
  11. Liang, R. I., Huang, S. E., & Chang, F. M. (1997). Prenatal diagnosis of ectopia cordis at 10 weeks of gesta-tion using two‐dimensional and three‐dimensional ultrasonography. Ultrasound in Obstetrics and Gynecology: The Official Journal of the Interna-tional Society of Ultrasound in Obstetrics and Gynecology, 10(2), 137-139. https://doi.org/10.1002/jcu.20134
  12. Carmi, R., & Boughman, J. A. (1992). Pentalogy of Cantrell: two patients and a review to determine prognostic factors for optimal approach. European journal of pediatrics, 167(1), 29-35. DOI: 10.1007/s00431-007-0578-9
  13. Carmi, R., & Boughman, J. A. (1992). Pentalogy of Cantrell: two patients and a review to determine prognostic factors for optimal approach. European journal of pediatrics, 167(1), 29-35. DOI: 10.1007/s00431-007-0578-9