Tetralogy of Fallot pathophysiology

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editors-In-Chief: Fahimeh Shojaei, M.D., Priyamvada Singh, M.B.B.S. [2], Keri Shafer, M.D. [3]; Omar Toubat; Assistant Editor-In-Chief: Kristin Feeney, B.S. [4]

Overview

Tetralogy of Fallot is a congenital heart lesion characterized by a constellation of four morphologic abnormalities present in the newborn heart. These features include a ventricular septal defect, overriding aorta, pulmonary stenosis, and right ventricular hypertrophy. The obstruction of right ventricular outflow in tetralogy of Fallot causes blood to shunt or flow from the right to left side of heart through the ventricular septal defect. This causes right ventricular hypertrophy and eventual right sided heart failure. There is flow of deoxygenated venous blood from the right side of the heart to the systemic circulation resulting in cyanosis.

Pathophysiology

Physiology

The normal physiology of heart development can be understood as follows:

• Subsequent to the lateral folding and looping events that give rise to the primitive heart tube are a series of complex septation processes that will ultimately complete morphogenesis of the four chambered heart.
• The goals of cardiac septation are two-fold:
  • To create four distinct cardiac chambers
  • To correctly position the great vessels relative to these chambers

https://en.wikipedia.org/wiki/File:2037_Embryonic_Development_of_Heart.jpg

Pathogenesis

• It is understood that tetralogy of fallot is the result of improper positioning of the outlet septum.
• In the normal heart, the outlet septum is an indistinguishable component of the crista supraventricularis that communicates with the septomarginal trabeculae to divide the right and left ventricular cavities.
• In Tetralogy of Fallot, proper ventricular septation is perturbed by anterocephalad displacement of the outlet septum relative to the septomarginal trabecula.
• The direct consequence of this misalignment is an overriding aortic orifice and a ventricular septal defect, resulting in an intracardiac right to left shunt of blood.
• In addition, anterocephalad displacement of the outlet septum indirectly predisposes the pulmonary trunk to stenosis in the setting of septoparietal trabecular hypertrophy.
• Together, the displacement of the outlet septum coupled with the hypertrophic arrangement of the septoparietal trabeculae account for the three anatomical cardinal defects in Tetralogy of Fallot - aortic dextroposition, interventricular communication (VSD), and pulmonary stenosis.
• The fourth defect - right ventricular hypertrophy - is a hemodynamic consequence of these three morphologic changes, as the right ventricle physiologically adapts to the increased resistance of a stenotic pulmonary trunk.

https://en.wikipedia.org/wiki/File:Tetralogy_of_Fallot.svg

Anatomy

https://en.wikipedia.org/wiki/File:Heart_tetralogy_fallot.svg This defect in outlet septum in turn leads to the four characteristic features: A: Pulmonic Stenosis Pulmonic stenosis is a right ventricular outflow tract obstruction A narrowing at (valvular stenosis, seen in approximately 20-25% case) or just below (infundibular stenosis, seen in around 50% of cases) the pulmonary valve. The stenosis is mostly the result of hypertrophy of the septoparietal trabeculae, however the deviated outlet septum is believed to play a role. The stenosis is the major cause of the malformations, with the other associated malformations acting as compensatory mechanisms to the pulmonic stenosis. The degree of stenosis varies between individuals with TOF, and is the primary determinant of symptoms and severity. This malformation is infrequently described as sub-pulmonary stenosis or subpulmonary obstruction. Tetralogy of Fallot with pulmonary atresia or pseudotruncus arteriosus is a severe variant in which there is complete obstruction of the right ventricular outflow tract and absence of the pulmonary trunk. In these individuals, there is complete right-to-left shunting of blood. The lungs are perfused via extensive collaterals from the systemic arteries. B: Overriding Aorta Overriding aorta is defined as when the aortic valve is not restricted to the left ventricle, thus having biventricular connections. The aortic root can be moved anteriorly or override the septal defect, but it is still to the right of the root of the pulmonary artery. The degree of override is quite variable, with 5-95% of the valve being connected to the right ventricle. C: Ventricular Septal Defect Ventricular septal defect is a hole between the two bottom chambers (ventricles) of the heart. The defect is centered around the outlet septum, the most superior aspect of the septum, and in the majority of cases is single and large. In some cases septal hypertrophy can narrow the margins of the defect. D: Right Ventricular Hypertrophy The right ventricle is more muscular than normal, causing a characteristic coeur-en-sabot (boot-shaped) appearance as seen by chest x-ray. Due to the misarrangement of the external ventricular septum, the right ventricular wall increase in size to deal with the increased obstruction to the right outflow tract. This feature is now generally agreed to be a secondary anomaly, as the level of hypertrophy generally increases with age. There is anatomic variation between the hearts of individuals with tetralogy of Fallot. The degree of right ventricular outflow tract obstruction varies between patients and is generally determines clinical symptoms and disease progression. {{#ev:youtube|ACRfFkxow7w}}

Embrylogy

• Embryologic studies show that tetralogy of Fallot is a result of anterior misalignment of the conal septum, resulting in the clinical combination of a ventricular septal defect (VSD), pulmonary stenosis, and an overriding aorta.
• Right ventricular hypertrophy is secondary to this combination of abnormalities, which causes resistance to blood flow from the right ventricle.
• Tetralogy of Fallot results in cyanosis, (hypoxia or low oxygenation) of the blood due to mixing of deoxygenated venous blood from the right ventricle with oxygenated blood in the left ventricle through the ventricular septal defect and preferential flow of both oxygenated and deoxygenated blood from the ventricles through the aorta because of obstruction to flow through the pulmonary valve.
• This is known as a right-to-left shunt.
• If pulmonary blood flow is dramatically reduced, pulmonary blood flow may depend on a patent ductus arteriosus (PDA) or bronchial collaterals.
• If obstruction of the right ventricular outflow tract is minimal, the intracardiac shunt may be mostly from left to right, and this may result in what is termed a pink tet or pink tetralogy.
• Although cyanosis is absent on clinical exam, laboratory testing will often show systemic oxygen desaturation.
• Children with tetralogy of Fallot may develop acute severe cyanosis or hypoxic tet spells.
• The mechanism underlying these episodes is not entirely clear, but may be due to spasm of the infundibular septum and the right ventricular outflow tract.
• Whatever the mechanism, there is an increase in resistance to blood flow to the lungs with increased preferential flow of desaturated blood to the systemic circulation.
• The child will often squat during a tet spell to improve venous return to the right side of the heart.
• Squatting increases the systemic vascular resistance and thereby shunts flow to pulmonary circuit.
• These spells can be fatal, and can occur in patients who are not cyanotic.

Genetics

• Genes involved in the pathogenesis of tetralogy of fallot include:
  • The cellular processes that underlie cardiogenesis are extensively regulated in the developing heart.
  • Proper cardiac development requires the complex orchestration of cardiac transcription factors and signaling pathways in a spatiotemporal specific manner.
  • Previous genetic studies demonstrated that mutations in numerous genes encoding cardiac transcription factors and cell signaling proteins have a role in the development of Tetralogy of Fallot.
  • Specifically, heterozygous mutations in NKX2-5, HAND1, TBX5, and GATA4 have been reported in familial forms of disease.
  • Many of these single gene mutations result in haploinsufficiency and suggest a dose dependent relationship between genetic expression and disease.
  • While the mechanistic basis of this relationship is currently poorly understood, it is hypothesized that disruption of the direct protein-protein interactions that allow these transcription factors to work synergistically impedes the activation of downstream targets and signaling pathways central to cardiac morphogenesis.
  • In addition, recent whole-exome sequencing investigations have introduced a novel role for epigenetic dysregulation in the pathogenesis of Tetralogy of Fallot.
  • Aberrant epigenetic modifications are thought to provide an alternative mechanism to perturb normal spatiotemporal expression of these essential developmental genes.

Associated Conditions

• Conditions associated with tetralogy of fallot include:
  • Left superior vena cava
  • Anomalies of the mitral valve
  • Anomalies of the tricuspid valve
  • Stenosis of the left pulmonary artery, in 40% of patients
  • A bicuspid pulmonary valve, in 40% of patients
  • Right sided aortic arch, in 25% of patients
  • Coronary artery anomalies, in 10% of patients
  • An atrial septal defect, in which case the syndrome is sometimes called a pentalogy of Fallot.
  • An atrioventricular septal defect
  • Partially or totally anomalous pulmonary venous return
  • Forked ribs and scoliosis
  • Associated abnormalities include cleft lip, cleft palate, hypospadias, skeletal and craniofacial abnormalities.

Gross Pathology

• On gross pathology characteristic features findings of tetralogy of fallot include:
  • Right ventricular hypertrophy
  • VSD
  • Overriding aorta
  • Subpulmonic stenosis

https://en.wikipedia.org/wiki/File:PLC_Fallots_tetralogy.jpg

Microscopic Pathology

There is no characteristic findings of tetralogy of fallot on microscopic histopathological analysis.

References

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