27 clinical MCQs in Cardiovascular System Pathology. Which foramen ovale closes in approximately 75% of individuals at birth?. Kenya, Africa and global...
Q1. Which foramen ovale closes in approximately 75% of individuals at birth?
Answer: Foramen ovale
Explanation: Closes by fusion of septum primum and secundum. Persists in 25% of adults as PFO. ---
Q2. Anatomical closure of the ductus arteriosus occurs through which process?
Answer: Intimal proliferation and fibrosis
Explanation: Functional closure via vasoconstriction occurs first. Anatomical closure takes several weeks through intimal proliferation and fibrosis. ---
Q3. Failure of which structure to adequately cover the ostium secundum results in ostium secundum ASD?
Answer: Septum secundum
Explanation: Ostium secundum ASD occurs when the septum secundum does not enlarge sufficiently to cover the ostium secundum. ---
Q4. Which VSD type is specifically more common in Asian patients?
Answer: Doubly committed subarterial VSD
Explanation: Situated in the outlet septum, bordered by fibrous continuity of aortic and pulmonary valves. ---
Q5. The fundamental embryological defect in Tetralogy of Fallot is
Answer: Anterior cephalad deviation of the outlet septum
Explanation: This single defect produces all four features of TOF — outlet VSD, pulmonary outflow obstruction, overriding aorta and RVH. ---
Q6. Which structure, when displaced apically, causes atrialization of the right ventricular inflow tract?
Answer: Septal leaflet of tricuspid valve
Explanation: This is Ebstein's anomaly. Apical displacement of the septal tricuspid leaflet causes the RV inflow to function as an atrial chamber. ---
Q7. In Transposition of Great Arteries, which embryological failure is directly responsible?
Answer: Resorption of subpulmonary instead of subaortic conus
Explanation: Normally the subaortic conus resorbs, moving the aorta posteriorly to connect with the LV. In TGA the wrong conus resorbs, keeping the aorta anterior and connected to the RV. ---
Q8. Which chromosomal abnormality is most specifically associated with coarctation of the aorta?
Answer: Turner syndrome
Explanation: Turner syndrome is specifically associated with coarctation of aorta and bicuspid aortic valve. Trisomy 21 is associated with AV canal defects. ---
Q9. Persistent truncus arteriosus always occurs alongside which other defect?
Answer: Ventricular septal defect
Explanation: The single great vessel overrides both ventricles, so a VSD is always present in persistent truncus arteriosus. ---
Q10. Sinus venosus ASD is specifically associated with anomalous drainage of pulmonary veins from which lung?
Answer: Right lung
Explanation: Right pulmonary veins drain anomalously into the SVC or right atrium due to the proximity of the sinus venosus defect to the SVC entry. ---
Q11. Which maternal teratogen is specifically associated with Ebstein's anomaly?
Answer: Lithium
Explanation: Maternal lithium use in first trimester is the specific teratogen classically associated with Ebstein's anomaly. ---
Q12. A restrictive VSD differs from a non-restrictive VSD in that it
Answer: May close spontaneously during childhood
Explanation: Restrictive VSDs cause no significant haemodynamic derangement and may close spontaneously, unlike large non-restrictive VSDs which cause progressive pulmonary hypertension. ---
Q13. Which congenital defect results from failure of both subpulmonary AND subaortic conus to resorb?
Answer: Double outlet right ventricle
Explanation: Failure of either conus to resorb produces double outlet anomalies of the RV. TGA results from resorption of the wrong conus. TOF results from malalignment, not failure of resorption. ---
Q14. The ostium primum is created during atrial septation by growth of which structure toward the AV canal?
Answer: Septum primum downward from the roof
Explanation: The septum primum grows downward creating the ostium primum inferiorly. As it grows, perforations form superiorly creating the ostium secundum. ---
Q15. VSD accounts for what percentage of all congenital heart disease?
Answer: 25%
Explanation: VSD is the most common congenital heart defect overall, accounting for 25% of all CHD. ---
Q16. Which component of the ventricular septum lies directly beneath the aortic valve?
Answer: Membranous septum
Explanation: The small membranous septum lies just underneath the aortic valve. Membranous VSDs often have inlet, outlet or trabecular extension. ---
Q17. In which CHD does the right ventricle inflow tract function haemodynamically as an atrial chamber?
Answer: Ebstein's anomaly
Explanation: Apical displacement of the septal tricuspid leaflet causes atrialization of the RV inflow tract — it receives atrial pressure and contracts out of synchrony with the functional RV. ---
Q18. Which of the following is the correct sequence of atrial septal development?
Answer: Septum primum → ostium primum → ostium secundum → septum secundum
Explanation: Septum primum grows down creating ostium primum. Perforations coalesce into ostium secundum. Then septum secundum develops to the right, leaving the fossa ovalis. ---
Q19. Which of the following maternal infections is a recognised cause of congenital heart disease?
Answer: Rubella
Explanation: Maternal rubella is a recognised environmental cause of CHD, particularly PDA and pulmonary stenosis. It is specifically listed among the environmental teratogenic causes of CHD. ---
Q20. In Tetralogy of Fallot, which level is the dominant site of right ventricular outflow obstruction?
Answer: Subvalvular (infundibular)
Explanation: The dominant obstruction in TOF is at the subvalvular/infundibular level due to hypertrophied infundibular myocardium from the malaligned outlet septum — not at the valve itself. ---
Q21. Coarctation of the aorta occurs most commonly at which location?
Answer: Juxtaductal — at the ductus arteriosus insertion
Explanation: Narrowing occurs just distal to the left subclavian artery at the site of ductus arteriosus insertion. ---
Q22. Which radiological finding is specifically associated with coarctation of the aorta?
Answer: Rib notching
Explanation: Caused by dilated intercostal collateral vessels eroding the inferior rib margins, developing to bypass the coarctation. ---
Q23. A patient with an untreated large VSD develops reversed cyanosis. Which term describes this end-stage complication?
Answer: Eisenmenger syndrome
Explanation: Chronic L→R shunting → pulmonary hypertension → pulmonary pressure exceeds systemic → shunt reverses to R→L → cyanosis. This is irreversible. ---
Q24. Patent foramen ovale in adults is specifically associated with which cerebrovascular complication?
Answer: Paradoxical embolism causing cryptogenic stroke
Explanation: Venous thrombus crosses from right to left atrium through the PFO entering systemic circulation, causing stroke without an obvious arterial source. ---
Q25. Ostium primum ASD is associated with a cleft in which specific valve leaflet?
Answer: Anterior mitral valve leaflet
Explanation: Both the ostium primum ASD and the cleft mitral leaflet result from the same endocardial cushion maldevelopment. Commonly seen in Down syndrome. ---
Q26. Which congenital heart defect is characterised by absence of a direct connection between the right atrium and right ventricle?
Answer: Tricuspid atresia
Explanation: There is no tricuspid valve orifice connecting RA to RV. Survival depends on an ASD for right-sided drainage and a VSD or PDA for pulmonary blood flow. ---
Q27. Hypoplastic left heart syndrome is more common in which sex?
Answer: Males
Explanation: Hypoplastic left heart is among the CHDs more common in males, alongside aortic stenosis, coarctation, pulmonary atresia, tricuspid atresia and TGA.