2005
DOI: 10.1016/j.echo.2004.09.030
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Ventricular septal hamartoma mimicking hypertrophic cardiomyopathy in a 41-year-old woman presenting with paroxysmal supraventricular tachycardia

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Cited by 18 publications
(11 citation statements)
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“…Overall, published data exist for 15 patients with hamartomas of mature cardiac myocytes, including our 7 new cases and 8 previously reported ones (Table 3) [1][2][3][4]6]. Ages ranged from 6 months to 74 years (mean, 28 years; median, 24 years).…”
Section: General Findingsmentioning
confidence: 78%
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“…Overall, published data exist for 15 patients with hamartomas of mature cardiac myocytes, including our 7 new cases and 8 previously reported ones (Table 3) [1][2][3][4]6]. Ages ranged from 6 months to 74 years (mean, 28 years; median, 24 years).…”
Section: General Findingsmentioning
confidence: 78%
“…Although it has been described as well demarcated, in our experience, poorly-defined lesions were the rule [1]. Lesions are characterized by disorganized myocytes that also underwent hypertrophy and by variable interstitial fibrosis and adiposity [1][2][3][4][5][6]. Myocyte disorganization or disarray includes 3 patterns: (1) haphazard, (2) herringbone, and (3) whorl or pinwheel.…”
Section: Cardiac Hamartomasmentioning
confidence: 98%
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“…Since minor surgical or biopsy specimens represent the only tissue available for evaluation removed from the ventricular septum, the distinction of HA from hypertrophic cardiomyopathy (HCM) may be impossible microscopically [1,7,15]. Therefore, the two can be differentiated only in light of clinical findings and imaging studies [1].…”
Section: Discussionmentioning
confidence: 99%