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Post-tuberculosis Aspergilloma in Undiagnosed Tetralogy of Fallot
Haseeb A Bhatti1, Shueeta Kumari2, Mohammad Hasan3
1Department of Internal Medicine, Jinnah Postgraduate Medical Centre, Karachi, PAK.
Insights
This case highlights a rare presentation of Tetralogy of Fallot (TOF) in a teenager, initially misdiagnosed as multi-drug resistant tuberculosis before confirming pulmonary aspergilloma. Congenital heart disease requires careful consideration in adult respiratory illness.
Area of Science:
- Cardiology
- Pulmonology
- Infectious Diseases
Background:
- Tetralogy of Fallot (TOF), a common congenital heart disease (CHD), typically presents in infancy but can remain undiagnosed into adulthood.
- Undiagnosed CHDs in adults are rare, presenting diagnostic challenges, especially with concurrent respiratory symptoms.
Observation:
- A teenage male with Tetralogy of Fallot presented with severe respiratory distress, hemoptysis, and fever, initially suspected as multi-drug resistant pulmonary tuberculosis (MDR-PTB).
- Despite anti-tuberculous treatment, the patient's condition did not improve, prompting further investigation.
- Chest imaging and bronchoalveolar lavage (BAL) ultimately confirmed pulmonary aspergilloma.
Findings:
- The patient was diagnosed with Tetralogy of Fallot (TOF) and pulmonary aspergilloma.
- Initial misdiagnosis of multi-drug resistant pulmonary tuberculosis (MDR-PTB) was due to overlapping symptoms and the known association of right-to-left shunts with pulmonary infections.
Implications:
- This case underscores the importance of considering congenital heart disease in adult patients with persistent respiratory symptoms, even in the presence of suspected infections.
- Clinicians should maintain a high index of suspicion for co-existing conditions like aspergilloma in patients with TOF and respiratory complaints.
- The correlation between pulmonary tuberculosis and right-to-left shunts, though rare, warrants clinical awareness.
Abstract:
Tetralogy of Fallot (TOF) is the most common congenital heart disease (CHD) with an incidence of four in every 1000 live births in Pakistan. Classically, these children present with central cyanosis in early life; however, milder defects may remain asymptomatic for months or even years. We report a malnourished and anemic teenage male, who was admitted with shortness of breath, hemoptysis, fever, palpitations, and weight loss. On examination, vitals were stable, except for oxygen saturation, which was 84% on pulse-oximeter. Bilateral basal coarse crepitations were present on respiratory examination with a markedly reduced air entry in the right upper zone. A 2-3/6 systolic ejection murmur was appreciated on cardiac examination. The chest X-ray was consistent with a collapsed right upper lobe with fibrosis. Echocardiography was consistent with findings of TOF. Based on sputum for acid-fast bacilli (AFB smear) and GeneXpert (Cepheid Inc., Sunnyvale, California, US) Mycobacterium tuberculosis/resistance to rifampin (MTB/RIF), the patient was diagnosed with multi-drug resistant pulmonary tuberculosis (MDR-PTB). However, when the patient didn't improve with anti-tuberculous therapy, a computed tomography (CT) scan chest was done, which raised a suspicion of aspergilloma. The culture and cytology of bronchoalveolar lavage (BAL) were done, which confirmed pulmonary aspergilloma. Undiagnosed congenital heart diseases are rare in adults. Pulmonary TB is rarely reported in right-to-left shunts; however, clinicians should maintain a suspicion of this correlation.
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