Discussion

Cantrell’s pentalogy was first described by Cantrell et al. in 1958. It comprises five major congenital defects at upper midline abdominal wall, lower sternum, anterior diaphragm, pericardial diaphragm, and intracardiac abnormalities. ^{Reference Cantrell, Haller and Ravitch1} A developmental failure of appropriated segments of the mesoderm is the embryologic background of the midline defects. ^{Reference Vazquez-Jimenez, Muehler and Daebritz2} It occurs in approximately 1 in 65,000 to 200,000 live births globally. ^{Reference Bianchi, Crombleholme and D’Alton3} Toyama’s classification scheme categorises Cantrell’s pentalogy into three classes. Class one involves a definite diagnosis with all five defects, while class two indicates a probable diagnosis with four defects, including ventral wall defect and intracardiac abnormalities. Class three signifies incomplete expression with a sternal abnormality and varied combinations of defects. ^{Reference Toyama4} Incomplete expression of the syndrome has been well-recognised in the literature, while the full spectrum has been rare. Complete pentalogy of Cantrell carries a high mortality whether being treated surgically or not, with most patients expiring during the early days of life. The surgical approach must be customised to the patient’s specific anatomy, acknowledging significant variations among cases. The primary goal is to achieve cardiopulmonary stability, which is usually already present. Next, it is crucial to cover the mediastinum to prevent sepsis, which, in cases such as ours, was present at birth due to in utero midline closure. Therefore, some patients may require staged surgery, while others can be corrected in a single procedure.

The degree of CHD is a source of major morbidity. ^{Reference Toyama4} Thus, we performed our own meta-analysis using patients with pentalogy of Cantrell reported in the literature from PubMed and Medline database to compare intracardiac findings, outcome of patients, and the most common associated malformations. With the following criteria, we included patients reported between 1972 and 2023, described in the English and Spanish literature. “Cantrell”, “Pentalogy of Cantrell”, “Cantrell’s pentalogy”, and “Cantrell syndrome” were used to search literature. We excluded patients reported in the literature without a definite diagnosis of Pentalogy of Cantrell, described in languages other than English or Spanish, and those reported after 2023 and not found using our literature search in PubMed or Medline. With these criteria, a total of 236 cases were included. 31% are female, 28% male, and 41% have an unreported biological sex. Of these cases, 22.5% were alive at the time of report, 39% were stillborn, 26.3% expired, and in 12.2%, the outcome was not reported.

The most common intracardiac findings in patients with Pentalogy of Cantrell are ventricular septal defect (32.6%), atrial septal defect (26.7%), tetralogy of Fallot (12%), double outlet right ventricle (7.6%), ductus arteriosus (7.6%), left superior vena cava (6.8%), pulmonary stenosis (6%), truncus arteriosus (5.1%), and single ventricle (5.1%), depicted in Table 1. Other intracardiac findings are dextrocardia (4.3%), anomalous pulmonary veins return (4.2%), hypoplastic left ventricle (4.2%), transposition of great arteries (3.4%), tricuspid atresia (3.4%), coarctation of the aorta (3%), arch anomalies (3%), single atrium (2.6%), atrioventricular septal defect (2.1%), double superior vena cava (1.7%), and anomalous coronary artery origin (1.2%). Less than 1% of patients presented with Ebstein’s anomaly, bicuspid pulmonary valve, atresia of aortic valve, hypoplastic right ventricle, mitral stenosis, pulmonary valve atresia, and single coronary ostium. One-fifth of patients had no specific intracardiac findings and one-tenth of patients had a normal cardiac examination. Extracardiac abnormalities were also reported including: ectopia cordis (45.8%), ventricular diverticulum (12.7%), aberrant common carotid artery (0.4%), and hypoplastic abdominal aorta (0.4%). The most common associated malformations seen with Pentalogy of Cantrell were exencephaly, spinal dysraphism, scoliosis, cleft lip, cleft palate, talipes equinovarus, limb agenesis, and low set ears. Although no specific genetic mutation has been identified as the cause of this syndrome, associations with trisomy 21, trisomy 18, Turner’s syndrome, and severe Goltz-Gorlin syndrome were observed in a small percentage of patients in our study. The prognosis for pentalogy of Cantrell depends on the type and severity of associated malformations, presence of ectopic heart, and intracardiac anomalies. Patients who underwent surgical repair around 8 months of age tend to have a better prognosis, whereas most non-survivors were operated on the first day after birth.

Table 1. Prevalence of intracardiac and extracardiac findings in Cantrell syndrome

The case highlights an unusual presentation of this syndrome as it is the first reported in literature to present with both tetralogy of Fallot and coarctation of the aorta. Intracardiac findings are a major prognostic factor in pentalogy of Cantrell; thus, comparing these findings across a 250-year span in our meta-analysis allows us to better understand the evolving patterns of cardiac anomalies associated with the syndrome. Through a comprehensive analysis of intracardiac findings over time, our aim is to refine patient care strategies and improve outcomes for patients diagnosed with pentalogy of Cantrell. Advances in research for pentalogy of Cantrell include a murine model developed by Aldeiri et al., in which genetic ablation of TGFβRII in Transgelin (Tagln) expressing cells results in midline closure anomalies similar to those seen in pentalogy of Cantrell. This establishes a reliable model to investigate the morphological alterations underlying Cantrell syndrome, providing the first mechanistic insight into the development of this syndrome. ^{Reference Aldeiri, Roostalu and Albertini5}