# Wolff-Parkinson-White syndrome: a masquerading clinical condition in an 8-year-old Nigerian girl

**Authors:** Olukemi T. Bamigboye-Taiwo, A. A. Afolabi, Oluwatosin Olorunmoteni, Samson Afolabi, Babajide Samson Adeyefa, OA Bayode, OO Bobo, EO Folami, Olayinka Otetubi, FA Olagunju, SBA Oseni, Oluwadare Ogunlade, JAO Okeniyi

PMC · DOI: 10.1186/s12872-025-05246-x · 2025-10-29

## TL;DR

An 8-year-old Nigerian girl with Wolff-Parkinson-White syndrome was misdiagnosed with malaria for years before receiving the correct diagnosis and treatment.

## Contribution

Highlights the diagnostic challenges of WPW syndrome in children and the need for increased awareness among healthcare providers in resource-limited settings.

## Key findings

- WPW syndrome can mimic other conditions like malaria, leading to misdiagnosis in children.
- Early recognition and intervention are crucial to prevent life-threatening complications.
- A high index of suspicion is needed for cardiac arrhythmias in children with unexplained recurrent symptoms.

## Abstract

Wolff-Parkinson-White (WPW) syndrome is a congenital abnormality of the cardiac conduction system characterized by the presence of an accessory pathway, which can predispose affected individuals to supraventricular tachycardia (SVT), atrial fibrillation, ventricular fibrillation, and sudden cardiac death. Despite its clinical significance, WPW syndrome is often underdiagnosed, particularly in resource-limited settings where cardiac arrhythmias may be misattributed to other conditions.

We report an eight-year-old Nigerian girl with WPW syndrome who was repeatedly misdiagnosed and managed for malaria over four years before an accurate diagnosis was established. She presented with recurrent episodes of chest discomfort, generalized weakness, nausea, and near-syncope. Each episode was treated as malaria, and symptoms resolved following treatment. During the most recent episode of the symptoms, she received care in a tertiary centre where SVT was identified following an electrocardiogram (ECG), heart rate was persistently about 250 beats per minute. Initial pharmacologic intervention with intravenous amiodarone was ineffective, necessitating external cardioversion to restore normal sinus rhythm. A post-recovery ECG confirmed a Wolf Parkinson White pattern.

WPW syndrome remains a diagnostic challenge in paediatric populations, where it can masquerade varying diseases, resulting in misdiagnosis. This case underscores the importance of a high index of suspicion for cardiac arrhythmias in children presenting with unexplained recurrent symptoms. Early recognition and appropriate intervention are crucial in preventing life-threatening complications associated with WPW syndrome. Increased awareness among healthcare providers can lead to improved diagnostic accuracy and better patient outcomes.

## Linked entities

- **Diseases:** Wolff-Parkinson-White syndrome (MONDO:0008685), malaria (MONDO:0005136), atrial fibrillation (MONDO:0004981), ventricular fibrillation (MONDO:0000190)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** weakness (MESH:D018908), malaria (MESH:D008288), ventricular fibrillation (MESH:D014693), atrial fibrillation (MESH:D001281), cardiac arrhythmias (MESH:D001145), SVT (MESH:D013617), congenital abnormality (MESH:D000013), syncope (MESH:D013575), sudden cardiac death (MESH:D016757), chest discomfort (MESH:D013898), WPW syndrome (MESH:D014927), nausea (MESH:D009325)
- **Chemicals:** amiodarone (MESH:D000638)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12574248/full.md

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Source: https://tomesphere.com/paper/PMC12574248