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Journal ArticleDOI

Hypertrophic cardiomyopathy and transmural myocardial infarction without significant atherosclerosis of the extramural coronary arteries.

TLDR
It is concluded that transmural myocardial infarction in the absence of significant coronary atherosclerosis is a not uncommon finding in a population of patients who had died from hypertrophic cardiomyopathy.
Abstract
Clinical and morphologic features of transmural myocardial infarction (associated with insignificant or absent atherosclerosis of the extramural coronary arteries) are described in seven patients with hypertrophic cardiomyopathy. Marked chronic congestive heart failure associated with supraventricular arrhythmias occurred in six of the seven patients, each of whom had no or mild left ventricular outflow tract obstruction under basal conditions. No patient had typical angina pectoris, and only one patient had clinically evident acute myocardial infarction. Infarction may have caused cardiac arrest in one other patient, but was "silent" in the remaining five patients. At necropsy, six of the seven patients had extensive myocardial scarring involving the ventricular septum, left ventricular free wall and one or both left ventricular papillary muscles; in four patients portions of the right ventricular wall were also scarred. Six patients had dilated ventricular cavities, including two who were known to have nondilated ventricular cavities earlier in their clinical course. It is concluded that transmural myocardial infarction in the absence of significant coronary atherosclerosis is a not uncommon finding (prevalence rate 15 percent) in a population of patients who had died from hypertrophic cardiomyopathy. Although transmural infarction is possibly a secondary event, it more likely contributes causally to the clinical deterioration of some patients with hypertrophic cardiomyopathy, leading to ventricular dilatation and progressive fatal cardiac failure.

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Citations
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Journal ArticleDOI

Hypertrophic cardiomyopathy: A Systematic review

Barry J. Maron
- 13 Mar 2002 - 
TL;DR: An appreciation that HCM, although an important cause of death and disability at all ages, does not invariably convey ominous prognosis and is compatible with normal longevity should dictate a large measure of reassurance for many patients.
Book

Coronary Microvascular Dysfunction

TL;DR: This review discusses the pathogenesis and management of coronary microvascular dysfunction and factors to consider in clinical management are the cause of the dysfunction and whether it is iatrogenic, whether obstructive coronary artery disease is present, and whether myocardial disease ispresent.
Journal ArticleDOI

The management of hypertrophic cardiomyopathy.

TL;DR: Hypertrophic cardiomyopathy is a complex cardiac disease with unique pathophysiologic characteristics and a great diversity of morphologic, functional, and clinical features as discussed by the authors, and the heterogeneity of the disease is accentuated by the fact that it afflicts patients of all ages.
Journal ArticleDOI

Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).

TL;DR: Seconde partie d'une revue: interrelations entre mecanismes physiopathologiques et manifestations cliniques ; traitement medical; traitement chirurgical.
References
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Journal ArticleDOI

Coronary vasospasm as a possible cause of myocardial infarction. A conclusion derived from the study of "preinfarction" angina.

TL;DR: In all 76 patients who underwent hemodynamic monitoring, 201thallium myocardial scintigraphy or angiography during angina, a vasospastic origin of the attacks was documented, and after infarction, complete thrombotic occlusion of the branch shown to undergo vasospasm was documented in two patients by angiographic.
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Idiopathic Hypertrophic Subaortic Stenosis: I. A Description of the Disease Based Upon an Analysis of 64 Patients

TL;DR: The finding of a murmur before the age of 1 year in 9 of the 64 patients, and the reports of IHSS in a stillborn baby and in several infants, as well as the association of IhSS with congenital cardiac malformations, all support the concept that the disease may, at least in some instances, be congenital.
Journal ArticleDOI

Coronary arterial spasm in Prinzmetal angina. Documentation by coronary arteriography.

TL;DR: Coronary arteriography should be attempted, if possible, during clinical attacks of pain in patients with Prinzmetal angina, even those who have a focal atherosclerotic obstruction may have additional distal coronary arterial spasm.
Journal ArticleDOI

Asymmetric Septal Hypertrophy: Echocardiographic Identification of the Pathognomonic Anatomic Abnormality of IHSS

TL;DR: The findings indicate that the detection of ASH identifies the pathognomonic anatomic abnormality in IHSS and includes a wider spectrum of patients (i.e. those without obstruction as well as clinically normal family members of patients with IhSS), and suggests that a more appropriate term for this disease entity is asymmetric septal hypertrophy or ASH.
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