Liu Deqing , Wu Jingqiang , Muhammad Tahir Khan , Li Tianyi , Zhang Lin , Xiao Haihao
{"title":"支气管动脉栓塞后造影剂诱发脑病：肺结核合并曲霉病1例报告并文献复习","authors":"Liu Deqing , Wu Jingqiang , Muhammad Tahir Khan , Li Tianyi , Zhang Lin , Xiao Haihao","doi":"10.1016/j.idcr.2025.e02367","DOIUrl":null,"url":null,"abstract":"<div><div>The current study analyzed a case of contrast-induced encephalopathy (CIE) following bronchial artery embolization (BAE) in a patient with hemoptysis due to pulmonary tuberculosis complicated by pulmonary aspergillosis. A 56-year-old male patient developed CIE after BAE was retrospectively analyzed. An ectopic bronchial artery originates from the proximal segment of the right vertebral artery. The patient developed CIE postoperatively, which resolved after treatment with corticosteroids and intracranial pressure reduction. A follow-up cranial MRI after 6 months showed complete resolution of previous edema. A literature review identified three cases of CIE after BAE, all presenting with hemoptysis, and symptom resolution within 3 days.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"42 ","pages":"Article e02367"},"PeriodicalIF":1.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Contrast-induced encephalopathy following bronchial artery embolization: A case report and literature review in a patient with pulmonary tuberculosis and aspergillosis\",\"authors\":\"Liu Deqing , Wu Jingqiang , Muhammad Tahir Khan , Li Tianyi , Zhang Lin , Xiao Haihao\",\"doi\":\"10.1016/j.idcr.2025.e02367\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The current study analyzed a case of contrast-induced encephalopathy (CIE) following bronchial artery embolization (BAE) in a patient with hemoptysis due to pulmonary tuberculosis complicated by pulmonary aspergillosis. A 56-year-old male patient developed CIE after BAE was retrospectively analyzed. An ectopic bronchial artery originates from the proximal segment of the right vertebral artery. The patient developed CIE postoperatively, which resolved after treatment with corticosteroids and intracranial pressure reduction. A follow-up cranial MRI after 6 months showed complete resolution of previous edema. A literature review identified three cases of CIE after BAE, all presenting with hemoptysis, and symptom resolution within 3 days.</div></div>\",\"PeriodicalId\":47045,\"journal\":{\"name\":\"IDCases\",\"volume\":\"42 \",\"pages\":\"Article e02367\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IDCases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2214250925002239\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IDCases","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214250925002239","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Contrast-induced encephalopathy following bronchial artery embolization: A case report and literature review in a patient with pulmonary tuberculosis and aspergillosis
The current study analyzed a case of contrast-induced encephalopathy (CIE) following bronchial artery embolization (BAE) in a patient with hemoptysis due to pulmonary tuberculosis complicated by pulmonary aspergillosis. A 56-year-old male patient developed CIE after BAE was retrospectively analyzed. An ectopic bronchial artery originates from the proximal segment of the right vertebral artery. The patient developed CIE postoperatively, which resolved after treatment with corticosteroids and intracranial pressure reduction. A follow-up cranial MRI after 6 months showed complete resolution of previous edema. A literature review identified three cases of CIE after BAE, all presenting with hemoptysis, and symptom resolution within 3 days.
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