ArticleEuropean heart journal. Case reports2022
Conservatively treated intramyocardial dissecting haematoma of the interventricular septum as a rare complication of acute myocardial infarction: a case report.
Article in European heart journal. Case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 7 citations in OpenAlex.
- Intraventricular Dissecting Hematoma Diagnosed and Followed up by Multimodality Imaging.Internal medicine (Tokyo, Japan) · 2025Article
- Autopsy revealed intramyocardial dissecting haematoma in the subacute phase of an anteroseptal myocardial infarction.European heart journal. Case reports · 2025Article
- Surgical treatment of intramyocardial dissecting hematoma-a case report and literature review.Frontiers in cardiovascular medicine · 2025Article
- Two Cases of Intramyocardial Dissecting Hematoma Diagnosed by Echocardiography.Journal of community hospital internal medicine perspectives · 2025Article
- Left ventricular dissecting haematoma and aneurysm formation in a patient who uses methamphetamines: a case report.BMC cardiovascular disorders · 2024Article
- Intramyocardial dissecting hematoma: A systematic review and pooled analysis of available literature.ARYA atherosclerosisReview
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
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Abstract
Background: Intramyocardial dissecting haematoma (IDH) is a rare and potentially life-threatening complication of acute coronary syndrome. So far only isolated case reports and case series have been published. Case summary: We report the case of a late presenting myocardial infarction (MI) complicated by IDH of the ventricular septum, following a successful percutaneous coronary intervention (PCI). The clinically inapparent septal mass was discovered during the routine transthoracic echocardiography and the final diagnosis of haematoma was made by magnetic resonance imaging. The patient remained clinically stable, and septal mass on repeated echocardiography showed gradual regression. Discussion: This report suggests that IDH can spontaneously resolve without surgical intervention. An urgent echocardiogram should be used to assess the vitality of the myocardial tissue, especially with late presenting MI with deep Q-waves on the electrocardiogram strip. Conservative treatment in haemodynamically stable patients with IDH following MI and PCI is a feasible solution.
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