Adil Zegmout, Ayman Farouki, Hanane Asri, Rachid Seddiki
{"title":"肺叶内嵌塞：病例报告","authors":"Adil Zegmout, Ayman Farouki, Hanane Asri, Rachid Seddiki","doi":"10.36347/sjmcr.2024.v12i05.061","DOIUrl":null,"url":null,"abstract":"Pulmonary sequestration is a rare malformation. It is characterised by a territory of non-functional bronchopulmonary tissue vascularised by one or more aberrant systemic arteries. We report the case of a 51-year-old man admitted to hospital with recurrent haemoptysis, a thoracic angioscan revealed left lower lobar sequestration by two systemic vessels. The patient was treated with a left lower lobectomy. Pulmonary sequestration remains a diagnostic and therapeutic challenge.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"86 13","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Intralobar Pulmonary Sequestration: A Case Report\",\"authors\":\"Adil Zegmout, Ayman Farouki, Hanane Asri, Rachid Seddiki\",\"doi\":\"10.36347/sjmcr.2024.v12i05.061\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Pulmonary sequestration is a rare malformation. It is characterised by a territory of non-functional bronchopulmonary tissue vascularised by one or more aberrant systemic arteries. We report the case of a 51-year-old man admitted to hospital with recurrent haemoptysis, a thoracic angioscan revealed left lower lobar sequestration by two systemic vessels. The patient was treated with a left lower lobectomy. Pulmonary sequestration remains a diagnostic and therapeutic challenge.\",\"PeriodicalId\":21448,\"journal\":{\"name\":\"Scholars Journal of Medical Case Reports\",\"volume\":\"86 13\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-05-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Scholars Journal of Medical Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.36347/sjmcr.2024.v12i05.061\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scholars Journal of Medical Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36347/sjmcr.2024.v12i05.061","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Pulmonary sequestration is a rare malformation. It is characterised by a territory of non-functional bronchopulmonary tissue vascularised by one or more aberrant systemic arteries. We report the case of a 51-year-old man admitted to hospital with recurrent haemoptysis, a thoracic angioscan revealed left lower lobar sequestration by two systemic vessels. The patient was treated with a left lower lobectomy. Pulmonary sequestration remains a diagnostic and therapeutic challenge.
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