A clinical perspective on surgical and diagnostic strategies for neonatal partial shone complex: Insights from a case report.

INTRODUCTION AND CLINICAL IMPORTANCE

Shone complex (SC) is a rare multilevel congenital heart disease (CHD) characterized by four left-sided heart obstructive lesions: parachute mitral valve, supravalvular mitral ring, subaortic stenosis, and coarctation of the aorta (CoA), accounting for 0.6-0.7 % of CHD cases.

CASE PRESENTATION

A 4-week-old male neonate presented with severe respiratory distress, tachycardia (150 beats/min), tachypnea (40/min), and hypoxia (80 % saturation). Blood pressure was 90/55 mmHg in the upper arms; lower extremity measurements were challenging. ECG showed a heart rate of 150 beats/min, normal sinus rhythm, left axis deviation, and left ventricular (LV) hypertrophy. Transthoracic echocardiography revealed mild concentric LV hypertrophy and reduced ejection fraction (45 %). A supramitral ring led to severe supravalvular mitral stenosis, and a bicuspid aortic valve caused moderate aortic stenosis. Suprasternal views confirmed severe CoA distal to the left subclavian artery. The patient underwent successful CoA repair at five months, with ongoing surveillance for other defects. One year later, he remained stable with no significant pressure gradient changes.

CLINICAL DISCUSSION

SC presents significant clinical challenge due to its associated congenital anomalies. Early echocardiographic diagnosis and timely surgical intervention are essential for optimizing patient outcomes, given the variability in severity and the potential for complications. Multidisciplinary management is crucial for addressing the complexities of this condition.

CONCLUSION

This case illustrates effective staged surgical management of partial SC, emphasizing early diagnosis and the utility of point-of-care ultrasound.