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Ann Thorac Surg 1997;64:830-831
© 1997 The Society of Thoracic Surgeons
Department of Cardiac Surgery, Ospedale Maggiore della Carità, Novara, Italy
Accepted for publication March 29, 1997.
| Abstract |
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| Introduction |
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He was referred to our institution 7 months later, when a routine chest roentgenogram showed a semicircular protuberance in the left inferior arch of the cardiac silhouette. Admission physical examination revealed an asymptomatic young man. Blood pressure was 120/80 mm Hg, heart rate was 70 beats/min, and no cardiac murmurs were noted. Two-dimensional echocardiography revealed the presence of a 3.5 x 4-cm cavity communicating with the left ventricle by a small defect in the anterobasal wall, which was first interpreted as a ventricular rupture contained by pericardial sac. However, a second examination of the images showed that the myocardial wall on both sides of the "neck" of the aneurysm was divided to form a sort of double Y. The two external Y branches joined to form the epicardial wall of the aneurysm, and the two Y branches closer to the left ventricular cavity joined to form a sort of diaphragm separating the left ventricular cavity from the aneurysm. Two small defects in the middle of the diaphragm allowed communication between the two cavities. A new transthoracic and transesophageal echocardiography confirmed these impressions (Fig 1
). The coronary angiography showed normal coronary arteries, with a patent left anterior descending artery curving smoothly around the base of the aneurysm. Left ventriculography confirmed the presence of a pseudoaneurysm.
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Intramyocardial dissecting hematoma as a complication of myocardial infarction has already been reported [2], and we believe that, in the single case we report, a myocardial dissection originating from a small tear in the endocardial wall of the anterior myocardium was responsible for pseudoaneurysm formation. The left anterior descending artery was patent and, even if a recanalization can be hypothesized, there was no suggestion of myocardial necrosis at the time of trauma. The lesion was very localized and the pathologic findings strongly supported a myocardial dissection because of the presence of a nearly complete diaphragm separating the aneurysm from the ventricular cavity. Our patient was asymptomatic, and his clinical course confirms that electrocardiography and the myocardial-specific isoenzyme of creatine kinase are poor indicators of traumatic myocardial injuries [3]. At present, even if the electrocardiogram and the level of the myocardial-specific isoenzyme of creatine kinase are within normal limits, we perform a transthoracic echocardiography as a routine procedure in patients suffering blunt chest trauma at the time of first observation and every 3 months for the first year. Echocardiography in this case was the key to a correct understanding of the mechanism of the lesion and was very helpful in planning the correct treatment. With regard to the surgical technique, the endoaneurysmal patch closure of the neck of the aneurysm was preferred to mattress pledgeted sutures to avoid any damage to the left anterior descending artery, which was very close to the medial border of the aneurysm itself. Probably a patch closure in the cases like the one we report, given the particular cause of the lesion, is more recommended to preserve the correct shape and function of the left ventricle.
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