Authors
- Dorijan Jagačić — Sunce Clinic, Zagreb, Croatia — ORCID: 0000-0003-3992-8466
- Ladislav Pavić — Sunce Clinic, Zagreb, Croatia — ORCID: 0000-0002-8048-998X
- Petar Medaković — Sunce Clinic, Zagreb, Croatia — ORCID: 0000-0002-7173-8286
- Kata Ćorić — Sunce Clinic, Zagreb, Croatia — ORCID: 0000-0003-4904-0380
- Dražen Lovrić — Sunce Clinic, Zagreb, Croatia — ORCID: 0000-0003-2702-5710
- Mladen Jukić — Sunce Clinic, Zagreb, Croatia — ORCID: 0000-0002-3927-3888
Keywords
myocardial bridging, ischemia, coronary CT angiography, genetics, palpitations
DOI
https://doi.org/10.15836/ccar2016.479Full Text
Myocardial bridging (MB) is an anatomical anomaly which is increasingly detected using coronary CT angiography (CCTA). The clinical significance of MB has been still insufficiently explored, moreover there are descriptions of this phenomenon in association with acute coronary syndrome, a variety of rhythm disorders and sudden deaths. After the breakthrough of the invasive coronary angiography (ICA), at which the so-called “milking”-effect may be observed, most commonly in the middle segment of the left anterior descending artery (LAD), in vivo diagnosis could be established. However, the ICA diagnosis showed a great discrepancy compared to post mortem diagnosis in this matter. According to some data, MB-prevalence is up to 50% (CCTA), as well as on autopsy studies, while at ICA this phenomenon has been observed in merely 5-10% of all cases. The presented case refers to a family, with both a father (56) and a son (26) being diagnosed with MB. They both had an unexplained recurrent thoracic pain i.e. palpitations. Thus, the son felt a sharp pain in the right chest whereby the pain spread in the mediastinum, across the right shoulder and the right side of the neck. In addition, he complained of paraesthesia in his extremities during physical activity. As regards his family medical history, on his mother’s side there were some cases of heart diseases. Patient’s general health status was normal. There were no signs of heart failure with a blood pressure of 140/80 mmHg. The standardized ECG in the emergency room was within normal ranges. Lab tests were within normal ranges, as well as chest X-ray. Both neurological and multiple cardiological examinations and findings were normal. The pain in the chest with a normal echocardiography led also to CCTA of the father and subsequently of the son. Shallow MB of the middle and distal LAD has been found in both patients. Additionally, insignificant plaques have been found in the LAD of the father (**Figures 1****,****2****,****3****,****4** and **5**). Both patients are stable under beta-blockers. In summary, we regard these symptoms to be associated with MB. Figure 1. Comparison of the myocardial bridging respectively atherosclerotic lesions of father and son. Figure 2. Calcified plaques in the proximal segment and myocardial bridging of the middle and distal part of the left anterior descending artery (father). Figure 3. Non-calcified plaques in the proximal segment and myocardial bridging of the middle and distal part of the left anterior descending artery (father). Figure 4. Myocardial bridging of the middle and distal part of the left anterior descending artery without atherosclerosis (son). Figure 5. Myocardial bridging of the middle and distal part of the left anterior descending artery without atherosclerosis (son). Owing to the collected data (1-3), we may conclude that MB should also be considered in association with cardiac symptoms that otherwise cannot be explained. The genetic basis of MB in certain families remains a topic of future research.
Literature
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