Pentalogy of Cantrell Cantrell pentalojisi

نویسندگان

  • Nilay Hakan
  • Mustafa Aydın
  • Ayşegül Zenciroğlu
  • Nurullah Okumuş
  • Nazmiye Nilgün Karadağ
  • Mehmet Şah İpek
چکیده

Ectopia cordis is a rare malformation presenting as an isolated lesion or as part of the Cantrell’s pentalogy syndrome characterized by midline closure defects. A preterm male baby who did not have antenatal follow-up was born by caesarean section with evisceration of the heart and major parts of the intraabdominal organs. Combination of these findings suggested the diagnosis of Cantrell’s pentalogy. Despite intensive care, the patient died soon after the birth due to the poor clinical state. In order to make contribution to literature about this subject, this rare case of neonate with Cantrell’s pentalogy was reported. Antenatal diagnosis, appropriate antenatal care and delivery in a hospital that is capable for treatment is important for a better prognosis.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

امفالوسل و قلب بیرون از قفسه سینه درنوزاد با Pentalogy of Cantrell

Background : Pentalogy of Cantrell is a very rare congenital anomaly which is diagnosed with severe thoracoabdominal defect, omphalocele, lower sternal defect, anterior diaphragmatic defect anterior pericardial defect and ectopia cordis.Pathogenesis is unknown, mesodermal developmental defects in 14-18 days after conception maybe responsible . Case Report: The case is newborn with omphalocele ...

متن کامل

Duplication of the ALDH1A2 gene in association with pentalogy of Cantrell: a case report

INTRODUCTION The pentalogy of Cantrell is rare clustering of congenital defects, first described by Cantrell and colleagues in 1958. The exact pathogenesis for the pentalogy remains unknown and no specific genetic abnormalities have been correlated; however, a failure of embryogenesis has been suspected. The microduplication of chromosome 15q21.3 (57,529,846 to 58,949,448) found in our patient ...

متن کامل

Pentalogy of Cantrell: case report and review of the literature.

Pentalogy of Cantrell is a syndrome that consists of five anomalies: a midline, upper abdominal wall abnormality; lower sternal defect; anterior diaphragmatic defect; diaphragmatic pericardial defect, and congenital abnormalities of the heart. The pathogenesis of this condition is not fully known yet, associations are common with this condition and treatment is extremely challenging. Prognosis ...

متن کامل

Antenatal Diagnosis of a Case of Pentalogy of Cantrell Associated with Phocomelia Cantrell Pentaloji ve Fokomelia Birlikteliği Saptanan Olgunun Antenatal Tanısı

Melek Çiçek, Kafkas Üniversitesi Tıp Fakültesi, Kadın Hastalıkları ve Doğum Anabilim Dalı, Tel. 0506 8609381 Email. [email protected] Geliş Tarihi: 05.12.2011 • Kabul Tarihi: 16.12.2011 ABSTRACT Pentalogy of Cantrell is a rare congenital syndrome; described as the association of partial or complete ectopia cordis, a supraumbilical abdominal wall defect, congenital heart defects, defects ...

متن کامل

Pentalogy of Cantrell: Is Echocardiography Sufficient in the Neonatal Period?

Pentalogy of Cantrell is a rare syndrome that is characterized by varying degrees of midline wall defects and congenital cardiac anomalies. A left ventricular diverticulum (LVD) is defined as partial ectopia cordis, can be part of the pentalogy of Cantrell, and can put the patient at risk of severe complications. Early diagnosis and ligation/resection of the LVD is important to prevent complica...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2011