Situs Inversus Dextrocardia with Cyanogen Complex Cardiopathy in a 16-Year-Old Albanian Male

Abstract

Introduction: Dextrocardia is rare in the general population and may be associated with significant additional cardiac malformations. It is commonly associated with additional cardiac malformations.
In this report, we have described the follow-up of a patient with Situs inversus dextrocardia and cyanotic complex cardiopathy in a 16-year-old Albanian male. The male patient, born in 2007 in Albania, was referred to our ambulatory at 6 months of life by a pediatrician cause of cyanosis and cardiac murmur. It was performed the echo Color Doppler examination, with the conclusion: situs inversus dextrocardia, unique ventricle, pulmonary arterial atresia. In 2008, a diagnostic catheterization was performed. The medico-chirurgical consultation has decided to leave the boy in natural history with a periodic follow–up. On 06.2009, in one of the routine examinations, there was evidence of hypertrophy of the unique ventricle associated with arterial hypertension. From that time, the patient is under medical treatment with periodic monitoring.
Conclusions: Regular follow-up of complex cyanogen congenital heart disease enhances healthcare for a high-risk target group. In a heave desaturations patient, the hypertension must be evaluated as a secondary complication of the primary problem.