{"title":"解剖异常导致气管受压1例:无名动脉综合征","authors":"Şule Gökçe, MD","doi":"10.54026/gjp/1006","DOIUrl":null,"url":null,"abstract":"Innominate artery compression syndrome is a rare congenital anomaly. The condition is an important consideration in the differential diagnosis of patients presenting with noisy breathing, a barky cough, and expiratory stridor. Here we report a case of Innominate Artery syndrome that presented with persistent and /or biphasic stridor in a 3-month-old. This case provides us to highlights the importance of unequivocally identifying the vascular anomalies and to emphasize once again the importance of detailed history and observing/hearing of the breathing during the examination.","PeriodicalId":274984,"journal":{"name":"Global Journal of Pediatrics (GJP)","volume":"35 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Case Presented with Tracheal Compression Caused by An Anatomical Anomaly: The Innominate Artery Syndrome\",\"authors\":\"Şule Gökçe, MD\",\"doi\":\"10.54026/gjp/1006\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Innominate artery compression syndrome is a rare congenital anomaly. The condition is an important consideration in the differential diagnosis of patients presenting with noisy breathing, a barky cough, and expiratory stridor. Here we report a case of Innominate Artery syndrome that presented with persistent and /or biphasic stridor in a 3-month-old. This case provides us to highlights the importance of unequivocally identifying the vascular anomalies and to emphasize once again the importance of detailed history and observing/hearing of the breathing during the examination.\",\"PeriodicalId\":274984,\"journal\":{\"name\":\"Global Journal of Pediatrics (GJP)\",\"volume\":\"35 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-03-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Global Journal of Pediatrics (GJP)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.54026/gjp/1006\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Global Journal of Pediatrics (GJP)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.54026/gjp/1006","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A Case Presented with Tracheal Compression Caused by An Anatomical Anomaly: The Innominate Artery Syndrome
Innominate artery compression syndrome is a rare congenital anomaly. The condition is an important consideration in the differential diagnosis of patients presenting with noisy breathing, a barky cough, and expiratory stridor. Here we report a case of Innominate Artery syndrome that presented with persistent and /or biphasic stridor in a 3-month-old. This case provides us to highlights the importance of unequivocally identifying the vascular anomalies and to emphasize once again the importance of detailed history and observing/hearing of the breathing during the examination.