Drug-coated balloons (DCBs) have emerged as an established alternative to drug-eluting stents (DES) in selected coronary settings, particularly for in-stent restenosis and small vessel disease. Their role in de novo coronary lesions during the acute phase of ST-elevation myocardi...
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Research Article10.9734/ajcr/2026/v9i1374
Background: Pulmonary artery stenosis (PAS) is an uncommon cause of right ventricular pressure overload, most often congenital. Acquired PAS caused by extrinsic vascular compression is rare but can have serious hemodynamic consequences, including progressive right ventricular dys...
Open access
Research Article10.9734/ajcr/2025/v8i1318
Background: Determining the infarct-related artery (IRA) in inferior ST-elevation myocardial infarction (STEMI) is generally guided by electrocardiographic (ECG) and angiographic characteristics. Diagnostic uncertainty increases when both the right coronary artery (RCA) and left...
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Research Article10.9734/ajcr/2026/v9i1353
Background: Large ventricular aneurysms (LVA) are now rare as the result of the widespread availability of percutaneous coronary intervention. Yet it presents adverse events such as recurrent angina, reduced ventricular stroke volume with congestive heart failure, mitral regurgit...
Open access
Research Article10.9734/ajcr/2026/v9i1347
Background: Peripartum cardiomyopathy (PPCM) is a rare but potentially life-threatening cause of heart failure occurring toward the end of pregnancy or in the months following delivery. Early recognition is essential to optimize outcomes. Case Presentation: We report the case of...
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Research Article10.9734/ajcr/2025/v8i1343
Rheumatoid arthritis is a systemic condition impacting not only joints but also various organs, with potential life-threatening consequences, particularly involving the heart. Pericardial damage is a prevalent cardiovascular manifestation that generally responds well to anti-infl...
Open access
Research Article10.9734/ajcr/2025/v8i1303
Background: Implanted central venous access devices are widely used in paediatric oncology patients for the administration of chemotherapy and supportive treatments. Although considered safe, catheter fracture with intravascular migration remains an uncommon but potentially serio...
Open access
Research Article10.9734/ajcr/2026/v9i1376
Background: Arrhythmogenic left ventricular cardiomyopathy (ALVC) is a rare and often underdiagnosed subtype of arrhythmogenic cardiomyopathy (ACM), characterized by predominant left ventricular involvement and a high risk of arrhythmias. In contrast to the classic right dominant...
Open access
Research Article10.9734/ajcr/2025/v8i1334
Dilated cardiomyopathy (DCM) is a heterogeneous myocardial disorder frequently linked to ischemic, hypertensive, or idiopathic etiologies. However, metabolic causes such as hypocalcemia, though rare, can lead to reversible myocardial dysfunction. Hypocalcemia-induced cardiomyopat...
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Research Article10.9734/ajcr/2026/v9i1372
HOUDA BACHRI, Mohamed Sarsari, Shihab Abu Baker, Oualid Kerrouani, Omar Nafii, Anass Mghrari, Jamila Zarzur & Mohammed Cherti·Asian Journal of Cardiology Research·2025
Aims: Dextrocardia is a rare congenital anomaly characterized by the right-sided position of the heart within the thoracic cavity. Although the prevalence of coronary artery disease (CAD) in this population is comparable to that of the general population, the diagnostic approach...
Open access
Research Article10.9734/ajcr/2025/v8i1288