We reported a case of a 53-year-old patient with coarctation of aorta and multiple aneurysmatic changes on aortic arch. Enhanced CT and reconstruction revealed significant coarctation and multiple aneurysmatic dilatation. The patient underwent stent implantation and was discharged with symptoms relived. Follow-up examination progression of aneurysms, however, without symptoms.

Human hydatid disease occurs after infection with Echinococcus granulosus, mainly involved liver and lung. Here we reported a 48-year-old woman, who presented to our hospital with intermittent chest pain. Transthoracic echocardiography, Enhanced CT and MRI of heart were performed, revealed the cyst located at the interventricular septum near the right ventricular apex. Other organs including lung and liver were not involved. The cyst was successfully removed, while postoperatively pathological biopsy confirmed the infection of Echinococcus granulosus, thus, she was finally diagnosed as isolated cardiac hydatid cyst.

In this case, we reported an old female with a rare combination of the Scimitar Syndrome and pulmonary artery aneurysm, and she presented with chest pain, fatigue and shortness when admitted in our hospital. Further cardiac examination including echocardiography and computed tomography angiogram were performed and revealed these rare anomalies. Surgical procedure was carried out to cure the patient. This patient stayed in ICU for few days without any major complications and discharged from hospital after 10 days.

We reported a case of a 3-month-old infant presented with supravalvular aortic stenosis with congenital right coronary artery deficiency. According to cardiovascular CT results, Doty technique was adopted to restore the aortic root geometry under cardiopulmonary bypass. An angioplasty was performed to establish right coronary blood flow at the same time. The patient had no abnormal cardiac symptoms after surgery.