Left Pulmonary Artery Agenesis in a Pediatric Patient – Case Report
نویسندگان
چکیده
منابع مشابه
Isolated Left Pulmonary Artery Agenesis: A Case Report
UNLABELLED Unilateral pulmonary artery agenesis without any cardiovascular malformation is a rare anomaly. We present the imaging findings of a patient who was diagnosed as isolated left pulmonary artery agenesis. A 27-year-old female patient was admitted to our hospital due to dyspnea during exercise for five years. Chest X-ray revealed minimally small left pulmonary hilum and left lung. She w...
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Introduction: Carcinoma of the larynx is an extremely uncommon clinical entity in pediatric age. The diagnosis of the laryngeal carcinoma is often delayed due to the low index of suspicion. The factors contributing to delayed diagnosis include the similarity of its symptoms to common benign lesions of the larynx in childhood and difficult examination of the larynx in pediatric patients. ...
متن کاملUnilateral Pulmonary Artery Agenesis in an Adult Patient with Cough and Hemoptysis: A Case Report
Unilateral pulmonary artery agenesis (UPAA) is an uncommon congenital anomaly and most patients present in neonatal period with respiratory symptoms. Left-sided pulmonary artery agenesis is less frequent than right-sided and is sometimes associated with cardiac anomalies. We report a patient with a history of repaired ventricular septal defect, who presented with cough and hemoptysis and the di...
متن کاملPulmonary Artery Agenesis: A Case Series
Pulmonary artery agenesis is a rare congenital abnormality in which atresia was encountered in the short segment of the right or left pulmonary arteries. It can be isolated or associated with cardiac abnormalities such as tetralogy of Fallot, septal defects or pulmonary stenosis. The majority of cases are diagnosed in childhood whereas some cases yield no symptoms until adulthood. We evaluated ...
متن کاملUnilateral pulmonary artery agenesis: a case series.
BACKGROUND Unilateral pulmonary artery agenesis (UPAA) is a rare congenital anomaly due to a malformation of the sixth aortic arch of the affected side during embryogenesis. The diagnosis is usually set at adolescence, however it can remain asymptomatic and late diagnosis is possible. DESCRIPTION We present a case series of three female patients, aged 18, 49 and 68 years old, with history of ...
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ژورنال
عنوان ژورنال: Journal of Interdisciplinary Medicine
سال: 2016
ISSN: 2501-8132
DOI: 10.1515/jim-2016-0017