ISSN : 1301-5680
e-ISSN : 2149-8156
TURKISH JOURNAL OF
THORACIC AND
CARDIOVASCULAR SURGERY
Turkish Journal of Thoracic and Cardiovascular Surgery     
Successful closure of ventricular septal defect in a patient with noncompaction of the left ventricular myocardium
Ömer Faruk Doğan, Metin Demircin
Department of Cardiovascular Surgery, Medical Faculty of Hacettepe University, Ankara

Abstract

Left ventricular noncompaction (LVNC) is a rare clinical condition characterized by numerous prominent intertrabecular recesses in the ventricle, and is an unclassified cardiomyopathy. The pathology has been almost invariably associated with other congenital cardiac malformations. We presented a twoyear- old patient with LVNC accompanied by ventricular septal defect (VSD). Two-dimensional echocardiography showed a perimembranous VSD, 8 mm in size, and LVNC. The ratio of left ventricular noncompacted/compacted myocardial layers was 4.2. Since there was no evidence for cardiomyopathy, the patient underwent open heart surgery for the closure of VSD. Four months after the operation, echocardiographic findings showed normal myocardial performance.

During the early phase of the embryo, ventricular intertrabecular spaces communicate with the ventricular cavity. As the heart develops, the myocardium becomes compacted and the mesh-like morphology disappears. Left ventricular noncompaction (LVNC), which is known as an unclassified cardiomyopathy, is thought to result from an arrest in endomyocardial morphogenesis. It is characterized by excessively prominent trabeculations in the affected ventricle(s), sometimes affecting the right ventricle and interventricular septum, as well.[1,2] This anomaly is generally associated with congenital obstructive lesions of the left or right ventricular outflow tract, such as pulmonary atresia with intact ventricular septum and aortic atresia.[3,4] Noncompaction of ventricular myocardium can be seen as an isolated malformation or associated with other congenital cardiac malformations.

Herein, we present a patient with LVNC concomitant with ventricular septal defect (VSD), who was successfully treated surgically via cardiopulmonary bypass (CPB). To our knowledge, this is the first case of LVNC concomitant with VSD that was surgically corrected by open heart surgery.

Case Presentation

A two-year-old patient was referred to our institution due to suspicion of a congenital cardiac defect. His heart rate was 110 beats/min in electrocardiography and a chest x-ray showed normal situs and an enlarged heart with a cardiothoracic ratio of 0.55. Two-dimensional echocardiography (2D-ECHO) showed a perimembranous VSD, 8 mm in size, and LVNC (Fig. 1a, 1b). Fortunately, left ventricular systolic function was not depressed and ejection fraction was 68%; however, there was a prominent trabeculation and recesses of left ventricle. The ratio of left ventricular noncompacted/compacted myocardial layers was 4.2, being diagnostic for noncompac tion. Data recorded at the catheterization laboratory were as follows: PA 57/23 mmHg (mean 36 mmHg), left ventricle 98 mmHg, right ventricle 14 mmHg, Ao 92/54 mmHg (mean 74 mmHg). There was no mitral or tricuspid valve insufficiency. The perimembranous VSD and left ventricular hypertrabeculation were also confirmed during cardiac catheterization (Fig. 2). Since there was no evidence for cardiomyopathy, the patient underwent open heart surgery for the closure of VSD. The defect was closed with the use of a Dacron patch and the patient was weaned from CPB. Inotropic support with dopamine or dobutamine was not required after the weaning from CPB. The patient's general and clinical condition improved after the operation. Postoperative echocardiography showed normal ejection fraction, and the patient was discharged from the hospital on the tenth postoperative day with a good clinical condition. Four months after the operation, echocardiographic findings showed normal myocardial performance.

Fig 1: Two-dimensional echocardiograms showing left ventricular noncompaction. (a) Parasternal long-axis view demonstrates a thin epicardial layer and an extremely thickened endocardial layer with prominent left ventricular trabeculations (white arrowheads), deep recesses in the apex and posterior wall of the ventricle and ventricular septal defect (gray arrowhead). (b) Modified parasternal long-axis view clearly shows prominent trabeculations and deep recesses (arrows) in the left ventricular free wall.

Fig 2: In the diastolic and systolic phases, anteroposterior and lateral views of cardiac catheterization clearly demonstrate hypertrabeculation and deep intertrabecular recesses in the left ventricle (arrowheads). VSD: Ventricular septal defect; Ao: Aorta; RV: Right ventricle; LV: Left ventricle.

Discussion

In the early phase of embryogenesis, the heart consists of a loose network of muscle fibers that normally condense gradually, and it becomes compacted with the disappearance of large intertrabecular spaces. It is thought that ventricular noncompaction represents an arrest in this process. Sengupta et al.[5] demonstrated that the myocardium was essentially 2-layered in the areas of noncompaction, with the noncompacted endocardiumto-epicardium ratio of ≥2. They measured the thickness during end-systole for better visualization of LVNC.[5] In our case, the ratio of left ventricular noncompacted/ compacted myocardial layers was 4.2.

Ventricular noncompaction may occur in isolation (isolated ventricular noncompaction) or may be associated with other congenital cardiac malformations.[6],[7] Echocardiography, magnetic resonance imaging, and angiography are the main imaging tools to diagnose ventricular noncompaction, but two-dimensional color Doppler echocardiography is the standard and first-line diagnostic tool. Despite an increasing awareness, there is still little knowledge regarding the diagnosis of this rare cardiomyopathy. The diagnosis of LVNC may easily be overlooked or delayed in particular cases presenting with heart failure due to depressed ventricular function. Delay in diagnosis is due to similarities between LVNC and other cardiomyopathies, and to the lack of familiarity of the referring physicians with its specific diagnostic pattern.

This rare abnormality is reported to be accompanied by three major conditions, namely, depressed ventricular function, systemic embolization, and ventricular arrhythmias that may sometimes be fatal. Because depressed ventricular function is diagnosed in the late period, patients are sometimes referred to clinics with the complaint of heart failure. Noncompaction primarily affects the left ventricle, but the right ventricle may also be involved.[4],[8],[9] Asymptomatic cases have normal systolic function and increased left ventricular enddiastolic pressure, mimicking restrictive cardiomyopathy. Most patients are initially asymptomatic,[10] though there are symptomatic cases.[1]

Similarities between LVNC and other cardiomyopathies sometimes make the differential diagnosis difficult. Familiarity of cardiologists with the pathology ensure early and correct diagnosis. Prominent multiple myocardial trabeculations and intertrabecular spaces within this trabecular structure which continue to the ventricular cavity are typical echocardiographic and angiocardiographic findings of LVNC.

The treatment of myocardial noncompaction is not different from that of other cardiomyopathies. Medical treatment is preferred at the beginning of congestive heart failure. Diuretics, angiotensin-converting enzyme inhibitors, and digitalis are preferred for medical treatment in patients with noncompaction of ventricular myocardium. In our case, medical treatment was not started because the patient had no symptoms of the myocardial failure during the preoperative and postoperative period. Transthoracic echocardiography, which shows clear and valuable data about systolic and diastolic functions, was performed periodically to monitor the status of myocardial performance.

To the best of our knowledge, no surgically treated case of LVNC combined with VSD has been reported previously. There is only one case report from our institution, in which congenitally corrected transposition of the great arteries accompanied by noncompaction of both ventricles was treated surgically under CPB.[2]

In conclusion, patients with VSD may have ventricular noncompaction without any manifestation of cardiomyopathy. Surgical correction should be performed in a single session in the early period of life. In these cases, progressive myocardial insufficiency may complicate the clinical condition, and may cause accelerated clinical deterioration. In addition, noncompaction should be suspected and investigated whenever ventricular function is depressed irrelevant to the accompanying heart defect, and if detected, appropriate medical management should be initiated to improve the myocardial performance in the early period of myocardial failure.

References

1) Chin TK, Perloff JK, Williams RG, Jue K, Mohrmann R. Isolated noncompaction of left ventricular myocardium. A study of eight cases. Circulation 1990;82:507-13.

2) Dogan R, Dogan OF, Oc M, Duman U, Ozkutlu S, Celiker A. Noncompaction of ventricular myocardium in a patient with congenitally corrected transposition of the great arteries treated surgically: case report. Heart Surg Forum 2005;8:E110-3.

3) Richardson P, McKenna W, Bristow M, Maisch B, Mautner B, O'Connell J, et al. Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies. Circulation 1996;93:841-2.

4) Alehan D, Dogan OF. Right ventricular noncompaction in a neonate with complex congenital heart disease. Cardiol Young 2005;15:434-6.

5) Sengupta PP, Mohan JC, Mehta V, Jain V, Arora R, Pandian NG, et al. Comparison of echocardiographic features of noncompaction of the left ventricle in adults versus idiopathic dilated cardiomyopathy in adults. Am J Cardiol 2004; 94:389-91.

6) Ichida F, Hamamichi Y, Miyawaki T, Ono Y, Kamiya T, Akagi T, et al. Clinical features of isolated noncompaction of the ventricular myocardium: long-term clinical course, hemodynamic properties, and genetic background. J Am Coll Cardiol 1999;34:233-40.

7) Oechslin EN, Attenhofer Jost CH, Rojas JR, Kaufmann PA, Jenni R. Long-term follow-up of 34 adults with isolated left ventricular noncompaction: a distinct cardiomyopathy with poor prognosis. J Am Coll Cardiol 2000;36:493-500.

8) Alehan D. Clinical features of isolated left ventricular noncompaction in children. Int J Cardiol 2004;97:233-7.

9) Ozkutlu S, Ayabakan C, Celiker A, Elshershari H. Noncompaction of ventricular myocardium: a study of twelve patients. J Am Soc Echocardiogr 2002;15:1523-8.

10) Junga G, Kneifel S, Von Smekal A, Steinert H, Bauersfeld U. Myocardial ischaemia in children with isolated ventricular non-compaction. Eur Heart J 1999;20:910-6.

Keywords : Ekokardiyografi; kardiyomiyopati; kalp defekti, doğuştan/komplikasyon/cerrahi; kalp septal defekti, ventriküler; kalp ventrikülü

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