2021•StatPearlsRequires access

Pentalogy of Cantrell

Muhammad Khawar Sana, Rebecca Maria Rentea

Open publisher page 1 citations

Abstract

Pentalogy of Cantrell (POC) is a collection of five congenital midline birth anomalies that present a distinctive challenge for providers and surgeons. Those five defects are of the heart, pericardium, diaphragm, sternum, and abdominal wall. This condition has been divided into two categories, complete or partial. Complete, as the name indicates, refers to the presence of all five defects, while others may present with only partial defects. It is also referred to as thoracoabdominal ectopia cordis, a condition where the heart is covered by an omphalocele-like membrane. Ectopia cordis (EC) is often found in fetuses with POC. Infants usually have multiple cardiac malformations with ventricular septal defect, and tetralogy of Fallot being the most common. POC may also carry genetic associations with trisomy 13, 18, 21, and Turner syndrome. The initial management addresses the lack of skin overlying the heart and abdominal cavity.Following initial management, additional surgery involve covering the midline defects, separating the abdominal and pericardial compartment, and repairing the diaphragm. Advanced reconstructive techniques are utilized for additional closure, including the use of flaps, skin closure only, and bioprosthetic agents. The intracardiac defects are often repaired at a later date. Survival depends on the associated cardiac anomalies and degree of thoracoabdominal defect.

About this research paper

What this paper is about

Pentalogy of Cantrell (POC) is a collection of five congenital midline birth anomalies that present a distinctive challenge for providers and surgeons. Those five defects are of the heart, pericardium, diaphragm, sternum, and abdominal wall. This condition has been divided into two categories, complete or partial. Complete, as the name indicates, refers to the presence of all five defects, while others may present with only partial defects. It is also referred to as thoracoabdominal ectopia cordis, a condition where the heart is covered by an omphalocele-like membrane. Ectopia cordis (EC) is often found in fetuses with POC. Infants usually have multiple cardiac malformations with ventricular septal defect, and tetralogy of Fallot being the most common. POC may also carry genetic associations with trisomy 13, 18, 21, and Turner syndrome. The initial management addresses the lack of skin overlying the heart and abdominal cavity.Following initial management, additional surgery involve covering the midline defects, separating the abdominal and pericardial compartment, and repairing the diaphragm. Advanced reconstructive techniques are utilized for additional closure, including the use of flaps, skin closure only, and bioprosthetic agents. The intracardiac defects are often repaired at a later date. Survival depends on the associated cardiac anomalies and degree of thoracoabdominal defect.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Pentalogy of Cantrell (POC) is a collection of five congenital midline birth anomalies that present a distinctive challenge for providers and surgeons. Those five defects are of the heart, pericardium, diaphragm, sternum, and abdominal wall. This condition has been divided into two categories, complete or partial. Complete, as the name indicates, refers to the presence of all five defects, while others may present with only partial defects. It is also referred to as thoracoabdominal ectopia cordis, a condition where the heart is covered by an omphalocele-like membrane. Ectopia cordis (EC) is often found in fetuses with POC. Infants usually have multiple cardiac malformations with ventricular septal defect, and tetralogy of Fallot being the most common. POC may also carry genetic associations with trisomy 13, 18, 21, and Turner syndrome. The initial management addresses the lack of skin overlying the heart and abdominal cavity.Following initial management, additional surgery involve covering the midline defects, separating the abdominal and pericardial compartment, and repairing the diaphragm. Advanced reconstructive techniques are utilized for additional closure, including the use of flaps, skin closure only, and bioprosthetic agents. The intracardiac defects are often repaired at a later date. Survival depends on the associated cardiac anomalies and degree of thoracoabdominal defect.

Key concepts: Medicine, Omphalocele, Pericardium, Tetralogy of Fallot, Intracardiac injection, Surgery, Sternum, Abdominal wall defect

Related papers

Back to paper searchBrowse research topicsOriginal source
Pentalogy of Cantrell — Research Paper | ScholarLens