{"title":"年轻男性心脏结节病合并多发左心室动脉瘤","authors":"Dibya Kumar Baruah, Venkateshwara Rao K, Anuradha D, Suresh Kumar P","doi":"10.1016/j.ihjccr.2023.05.002","DOIUrl":null,"url":null,"abstract":"<div><p>Multiple left ventricular aneurysms (LVAs) are distinctly rare and have varied etiology. Manifestations of these entities are similar to the commonest LVA of ischemic origin. Our case is a young male with multiple LVAs with histological evidence of chronic granulomatous disease, and cardiac imaging suggestive of sarcoidosis, responded well to immunosuppressive therapy.</p></div>","PeriodicalId":100653,"journal":{"name":"IHJ Cardiovascular Case Reports (CVCR)","volume":"7 2","pages":"Pages 46-49"},"PeriodicalIF":0.0000,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cardiac sarcoidosis with multiple left ventricular aneurysms (LVAs) in a young male\",\"authors\":\"Dibya Kumar Baruah, Venkateshwara Rao K, Anuradha D, Suresh Kumar P\",\"doi\":\"10.1016/j.ihjccr.2023.05.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Multiple left ventricular aneurysms (LVAs) are distinctly rare and have varied etiology. Manifestations of these entities are similar to the commonest LVA of ischemic origin. Our case is a young male with multiple LVAs with histological evidence of chronic granulomatous disease, and cardiac imaging suggestive of sarcoidosis, responded well to immunosuppressive therapy.</p></div>\",\"PeriodicalId\":100653,\"journal\":{\"name\":\"IHJ Cardiovascular Case Reports (CVCR)\",\"volume\":\"7 2\",\"pages\":\"Pages 46-49\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IHJ Cardiovascular Case Reports (CVCR)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468600X2300021X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IHJ Cardiovascular Case Reports (CVCR)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468600X2300021X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Cardiac sarcoidosis with multiple left ventricular aneurysms (LVAs) in a young male
Multiple left ventricular aneurysms (LVAs) are distinctly rare and have varied etiology. Manifestations of these entities are similar to the commonest LVA of ischemic origin. Our case is a young male with multiple LVAs with histological evidence of chronic granulomatous disease, and cardiac imaging suggestive of sarcoidosis, responded well to immunosuppressive therapy.