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A Hidden Diagnosis Behind Giant Inverted T-waves: Recognizing Apical Hypertrophic Cardiomyopathy in a Young Adult
Abdul Rehman1, Muzamil Aslam Chaudhary2, Muhammad Yahya Khan3,4
1Emergency Department, St. Luke's General Hospital, Kilkenny, IRL.
Insights
Apical hypertrophic cardiomyopathy (ApHCM) can cause chest pain in young adults. Early cardiac MRI is crucial for diagnosing ApHCM and preventing misdiagnosis, especially with unusual ECG findings.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Cardiomyopathies
Background:
- Chest pain in young adults is a diagnostic challenge, often mimicking acute coronary syndrome.
- Non-cardiac causes are more common, but cardiac conditions like hypertrophic cardiomyopathy must be considered.
- Apical hypertrophic cardiomyopathy (ApHCM) is a rare form of hypertrophic cardiomyopathy.
Abstract:
Chest pain in young adults can pose a diagnostic challenge, often raising concerns for acute coronary syndrome but more commonly resulting from non-cardiac causes. We report a case of apical hypertrophic cardiomyopathy (ApHCM) in a 27-year-old man, presenting with episodic chest pain and striking ECG abnormalities but normal coronary angiography. This case underscores the value of recognizing characteristic ECG patterns and the role of cardiac MRI in confirming ApHCM, a rare but clinically significant condition that can otherwise be misdiagnosed. Awareness of these findings in young patients without traditional cardiovascular risk factors is essential, as early MRI can establish the diagnosis and prevent unnecessary invasive procedures.
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