Person: OTÇU TEMUR, HAFİZE
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Publication Metadata only Recurrent Elevation of Troponin Levels in Acute Myocarditis: Is it a Sign of Ventricular Tachycardia?(2020-07-01T00:00:00Z) Yozgat, Can Yilmaz; YEŞİLBAŞ, Osman; UZUNER, SELÇUK; SARITAŞ, BETÜL; ERGÖR, Serap Nur; OTÇU TEMUR, Hafize; YOZGAT, Yılmaz; YEŞİLBAŞ, OSMAN; UZUNER, SELÇUK; SARITAŞ, BETÜL; ERGÖR, SERAP NUR; OTÇU TEMUR, HAFİZE; YOZGAT, YILMAZPublication Metadata only Development of Myocardial Infarction in a 12-Year-Old Female after the Use of Inhaled Salbutamol(2020-12-01T00:00:00Z) Yozgat, Can Yilmaz; UZUNER, SELÇUK; OTÇU TEMUR, Hafize; ERGÖR, Serap Nur; GULİYEVA, AYNUR; Tahaoglu, Irmak; Coban, Senay; YOZGAT, YILMAZ; UZUNER, SELÇUK; OTÇU TEMUR, HAFİZE; ERGÖR, SERAP NUR; GULİYEVA, AYNUR; YOZGAT, YILMAZAnomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) accounts for 0.023% of all cases reported in pediatric patients. According to literature, only a handful of ALCAPA patients are able to reach adulthood. Clinical manifestations of ALCAPA range from fatigue during exercise to sudden death in adulthood. Herein, we described a 12-year-old symptomatic patient with ALCAPA who had severe chest pain after using salbutamol treatment for presumed asthma. ALCAPA is one of the curable versions of myocardial ischemia and infarction in childhood. Due to clinical findings in conjunction with electrocardiogram and echocardiography, a computed tomography scan with coronary angiography was performed and the diagnosis of ALCAPA was confirmed. We presented this case because ALCAPA-related myocardial ischemia and infarction in children are rare with only sporadic cases reported. This case illustrated the need for close monitoring and surgery as the best treatment for ALCAPA associated with myocardial infarction.Publication Metadata only Balanced Double Aortic Arch Causing Persistent Respiratory Symptoms Mimicking Asthma in an Infant(2020-09-01T00:00:00Z) OTÇU TEMUR, Hafize; Yozgat, Can Yilmaz; UZUNER, SELÇUK; Ugurlucan, Murat; YAZAN, HAKAN; ÇAKIR, Erkan; YOZGAT, Yılmaz; OTÇU TEMUR, HAFİZE; UZUNER, SELÇUK; YAZAN, HAKAN; ÇAKIR, ERKAN; YOZGAT, YILMAZDouble aortic arch (DAA) is a common form of complete vascular ring. The state of the condition leads to upper airway impediment and compression of the esophagus. A balanced DAA is an extremely rare anomaly. The anatomical aberration cannot be easily diagnosed with echocardiography when an infant has chronic respiratory distress. Herein, we present the case of an 11-month-old girl who had chronic respiratory distress and a balanced DAA.