Person: YAKUT, KAHRAMAN
8 results
Search Results
Now showing 1 - 8 of 8
Publication Metadata only A Report of Brugada Syndrome Presenting with Cardiac Arrest Triggered by Verapamil Intoxication(2017-11-01) Yakut, KAHRAMAN; Erdogan, Ilkay; Varan, Birgul; Atar, Ilyas; YAKUT, KAHRAMANBackground: Brugada syndrome is a disease characterized by a specific electrocardiographic pattern and an increased risk of sudden cardiac death. We present this case with the updated literature to emphasise the need to consider the diagnosis of Brugada syndrome in patients admitted to the emergency ward with sudden cardiac arrest.Publication Metadata only The results of interventional catheterization in infants weighing under 2,000 g(2019-07-01) Varan, Birgul; Tokel, N. Kursad; Yakut, KAHRAMAN; Erdogan, Ilkay; Ozkan, Murat; YAKUT, KAHRAMANBackground: The aim of this study was to evaluate the early and mid-term results of interventional cardiac catheterization and procedure-related complications in infants weighing <2,000 g.Publication Metadata only Case report of a rarely seen long-segment middle aortic syndrome(2017-03-01) Yakut, KAHRAMAN; Erdogan, Ilkay; YAKUT, KAHRAMANMiddle aortic syndrome (MAS) follows a course with distal thoracic and abdominal aorta stenosis. It is a rare disease that is usually diagnosed after the first decade of life. Clinical reflection of MAS is often in the form of hypertension and claudication in the lower extremities. Its etiology is unclear, but is known to be associated with congenital or acquired diseases. This pathology, which is accompanied by malignant hypertension, often does not respond to medical treatment. In patients with MAS, surgical treatment is first line recommendation to prevent complications such as hypertension, heart failure, intracranial bleeding, or aortic rupture. In order to draw attention to this disease, presently described is case of high blood pressure detected during routine examination of a child who had no complaint, and discovery of long-segment stenosis in the abdominal aorta identified with echocardiography and conventional angiography.Publication Metadata only Asymptomatic giant congenital left atrial aneurysm(2019-01-01T00:00:00Z) Yakut, KAHRAMAN; Varan, Birgul; Erdogan, Ilkay; YAKUT, KAHRAMANCongenital aneurysm of the left atrial appendage can be caused by congenital dysplasia of the pectinate muscles and may be accompanied by a congenital absence of the pericardium. Symptoms generally manifest after two decades and the most common symptom is atrial arrhythmia in the form of atrial fibrillation / flutter. A four year-old patient with no symptoms underwent an echocardiographic examination for the investigation of a heart murmur. Echocardiographic examination revealed a large cystic lesion occupying the left hemithorax and compressing the left ventricle. The patient was referred to our center. The lesion caused displacement of the heart rightward behind the sternum which made the examination difficult. We aimed to present this rare case of giant left atrial appendage aneurysm in the light of current literature.Publication Metadata only Kawasaki disease presented with unusual findings: Report of two cases Sira Disi Bulgularla Seyreden Kawasaki Hastaligi: Iki Olgu(2017-01-01) Yakut, KAHRAMAN; Ecevit, Zafer; Varan, Birgül; Erdogan, Ilkay; Güngör, Sirel Gür; YAKUT, KAHRAMANPublication Metadata only Diagnosis and treatment of abnormal left coronary artery originating from the pulmonary artery: A single-center experience(2019-12-01T00:00:00Z) Yakut, KAHRAMAN; Tokel, Niyazi Kursad; Ozkan, Murat; Varan, Birgul; Erdogan, Ilkay; Aslamaci, Mehmet Sait; YAKUT, KAHRAMANObjective: We aimed to review symptoms, findings, surgical treatment options, short- and mid-term outcomes, and reoperation rate of patients diagnosed with of left coronary artery from the pulmonary artery (ALCAPA) of an anomalous origin in our institution.Publication Metadata only Case report and the surgical treatment of two cases with pulmonary atresia in which pulmonary arteries is circulated by coronary arteries(2018-04-01) Yakut, KAHRAMAN; Tokel, Kursad; Varan, Birgul; Erdogan, Ilkay; Ozkan, Murat; YAKUT, KAHRAMANPulmonary atresia (PA) and ventricular septal defect (VSD) can occur in a variety of ways, from simple valve atresia to a condition in which circulation to the pulmonary bed occurs through collateral arteries separated from the aorta and there are no real pulmonary arteries, or they are present but hypoplastic. The size of the pulmonary arteries and concomitant complex cardiac lesions are important in making decisions about treatment and correctional alternatives. While complete correction surgeries in the style of a correction of tetralogy of Fallot are performed in simpler cases, many very invasive procedures are also performed and the resulting quality of life is very variable. The size of the pulmonary artery and its branches and the presence of accompanying collateral vessels are determining factors in the management of the disease. In this report, 2 cases of VSD and PA, in which the circulation of the pulmonary arteries was through the coronary arteries, diagnosed as a result of echocardiography performed following murmurs heard during examination, are described. The first patient was 40 days old and the second was 2 days old. In the second case, diagnosis was confirmed by catheter angiography, and in the first case, the final diagnosis was made during surgery. The aim of this report is to emphasize the importance of pulmonary artery size, the presence of pulmonary confluence, the origin of circulation, and concomitant collateral arteries when considering treatment methods.Publication Metadata only Diagnosis and surgical treatment of aortopulmonary window: Our single-center experience(2018-01-01) Yakut, KAHRAMAN; Ozkan, Murat; Varan, Birgul; Erdogan, Ilkay; Aslamact, Sait; YAKUT, KAHRAMANBackground: In this study, we aimed to report our single-center experience in aortopulmonary window and review clinical signs, symptoms, surgical correction techniques, and long-term outcomes.