MCQ: Cardiovascular System Pathology

27 clinical MCQs in Cardiovascular System Pathology. Which foramen ovale closes in approximately 75% of individuals at birth?. Kenya, Africa and global...

Questions, Answers & Explanations

  1. 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. ---

  2. 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. ---

  3. 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. ---

  4. 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. ---

  5. 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. ---

  6. 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. ---

  7. 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. ---

  8. 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. ---

  9. 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. ---

  10. 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. ---

  11. 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. ---

  12. 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. ---

  13. 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. ---

  14. 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. ---

  15. 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. ---

  16. 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. ---

  17. 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. ---

  18. 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. ---

  19. 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. ---

  20. 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. ---

  21. 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. ---

  22. 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. ---

  23. 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. ---

  24. 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. ---

  25. 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. ---

  26. 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. ---

  27. 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.

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