Introduction: Thyrotoxicosis typically manifests as a hypermetabolic state characterized by tachyarrhythmias, such as sinus tachycardia or atrial fibrillation. Bradyarrhythmia, specifically atrioventricular block (AVB), is a rare and atypical cardiac manifestation. While Graves’ disease is the leading cause of hyperthyroidism, non-autoimmune etiologies must be considered when thyroid-stimulating antibodies are absent. The exact mechanism for AVB in thyrotoxicosis remains unclear but may involve myocardial inflammation of the conduction system or autonomic dysfunction. Case: A 16-year-old male with no previous medical history presented with a sudden syncopal attack. Clinical evaluation revealed a complete heart block (CHB) in association with biochemical evidence of thyrotoxicosis, requiring a temporary transcutaneous pacemaker insertion. There were no features of Graves’ disease, such as exophthalmos and thyroid acropachy, and further investigation showed a negative thyroid receptor antibody (TRAb) titer with no family history of thyroid disorders. Thyroid ultrasonography showed increased vascularity, while scintigraphy imaging showed diffuse, homogeneous, and increased uptake in both thyroid lobes. The combination of negative serology and the absence of a family history, along with a hyperfunctional state on imaging, likely suggests a rare presentation of sporadic, non-autoimmune, nonfamilial form of thyrotoxicosis. Following the initiation of anti-thyroid therapy, the CHB completely resolved without the need for further cardiological intervention. He achieved a complete clinical remission after a few months and is being planned for radioactive iodine therapy. Conclusion Most of the thyrotoxicosis-associated CHB reported in the literature was due to Graves’ disease or some forms of autoimmune thyrotoxicosis, with auto-antibodies and activated lymphocytes having a role in the pathogenesis of the CHB. CHB in association with a non-autoimmune, non-familial form of thyrotoxicosis is indeed rare, and as this case illustrates, it completely went into spontaneous sinus rhythm upon initiation of conventional anti-thyroid therapy. This rare presentation of CHB is believed to have a benign clinical course.
Thyrotoxicosis ; Heart Block

Epicardial lipomatous hypertrophy (ELH) is a rare histologically benign condition characterized by excessive accumulation of epicardial fat. We report a case of a 68-year-old female who experienced reduced effort tolerance for the past year. A transthoracic echocardiogram revealed a suspicious circumferential mass around the heart. Cardiac magnetic resonance (CMR) was subsequently performed and identified a 13- to 15-mm-thick layer of epicardial fat surrounding the myocardium, with a small pericardial effusion at the lateral wall. Cardiac function was preserved, and her symptoms were ultimately attributed to atherosclerotic coronary disease, which was treated accordingly. This case highlights the importance of using complimentary multimodal imaging such as CMR, to differentiate between ELH and others, for accurate diagnosis and further management.