A Hidden Diagnosis Behind Giant Inverted T-waves: Recognizing Apical Hypertrophic Cardiomyopathy in a Young Adult
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.
Authors
- Fatima Bibi (ORCID: https://orcid.org/0000-0001-9747-0815)
- Manisha Chaudhary (ORCID: https://orcid.org/0009-0005-5746-656X)
- Abdul Rehman (ORCID: https://orcid.org/0000-0002-4364-5613)
- Muhammad Khan (ORCID: https://orcid.org/0000-0001-7760-2374)
- Syeda Zoya Chishti
Institutions
- Punjab Medical College (PK)
- Allied Hospital (PK)
- Wrightington, Wigan and Leigh NHS Foundation Trust (GB)
- University of Faisalabad (PK)
- St. Luke's General Hospital (IE)
- Pakistan Institute of Medical Sciences (PK)
Publication Details
- Journal
- Cureus
- Published
- 2025-08-31
- DOI
- https://doi.org/10.7759/cureus.91364
- Primary Topic
- Cardiomyopathy and Myosin Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00