Bakkali Tarik, H. M. Amine, Lekhel Brahim, Sefiani Yasser, M. Abbes, B. Younes
{"title":"一名年轻的白塞氏病患者的致命胸腹动脉瘤扩张","authors":"Bakkali Tarik, H. M. Amine, Lekhel Brahim, Sefiani Yasser, M. Abbes, B. Younes","doi":"10.5812/acvi.38067","DOIUrl":null,"url":null,"abstract":"Introduction: Arterial involvement in Behcet's disease has been previously described. We report a rare case of a large and longsegment thoracoabdominal aneurysm, which was associated with Behcet's disease and had an unfavorable evolution. Case Presentation: A 23-year-old man was diagnosed with Behcet's disease, as revealed by a carotid aneurysm, and was treated with a prosthetic graft reconstruction as well as immunosuppressive therapy. The patient was lost to follow-up. He stopped the medications of his own will 1 month after his discharge from the hospital. Two years later, he presented with chest pain of 1 week's duration. Alarge aneurysminvolving a long aorta segment from the sinus of Valsalva to the abdominal aorta above the renal arteries was identified by computed tomography angiography. Unfortunately, the patient died despite immunosuppressive therapy and before any surgical or endovascular intervention could be performed. Conclusions: This rare observation supports the role of immunosuppressive therapy in preventing the recurrence of lifethreatening vascular lesions in the management of Behcet's disease.","PeriodicalId":429543,"journal":{"name":"Archives of Cardiovascular Imaging","volume":"136 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fatal expanding thoracoabdominal aneurysm in known but mistreated behcet's disease in a young patient\",\"authors\":\"Bakkali Tarik, H. M. Amine, Lekhel Brahim, Sefiani Yasser, M. Abbes, B. Younes\",\"doi\":\"10.5812/acvi.38067\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Arterial involvement in Behcet's disease has been previously described. We report a rare case of a large and longsegment thoracoabdominal aneurysm, which was associated with Behcet's disease and had an unfavorable evolution. Case Presentation: A 23-year-old man was diagnosed with Behcet's disease, as revealed by a carotid aneurysm, and was treated with a prosthetic graft reconstruction as well as immunosuppressive therapy. The patient was lost to follow-up. He stopped the medications of his own will 1 month after his discharge from the hospital. Two years later, he presented with chest pain of 1 week's duration. Alarge aneurysminvolving a long aorta segment from the sinus of Valsalva to the abdominal aorta above the renal arteries was identified by computed tomography angiography. Unfortunately, the patient died despite immunosuppressive therapy and before any surgical or endovascular intervention could be performed. Conclusions: This rare observation supports the role of immunosuppressive therapy in preventing the recurrence of lifethreatening vascular lesions in the management of Behcet's disease.\",\"PeriodicalId\":429543,\"journal\":{\"name\":\"Archives of Cardiovascular Imaging\",\"volume\":\"136 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-02-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives of Cardiovascular Imaging\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5812/acvi.38067\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Cardiovascular Imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5812/acvi.38067","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Fatal expanding thoracoabdominal aneurysm in known but mistreated behcet's disease in a young patient
Introduction: Arterial involvement in Behcet's disease has been previously described. We report a rare case of a large and longsegment thoracoabdominal aneurysm, which was associated with Behcet's disease and had an unfavorable evolution. Case Presentation: A 23-year-old man was diagnosed with Behcet's disease, as revealed by a carotid aneurysm, and was treated with a prosthetic graft reconstruction as well as immunosuppressive therapy. The patient was lost to follow-up. He stopped the medications of his own will 1 month after his discharge from the hospital. Two years later, he presented with chest pain of 1 week's duration. Alarge aneurysminvolving a long aorta segment from the sinus of Valsalva to the abdominal aorta above the renal arteries was identified by computed tomography angiography. Unfortunately, the patient died despite immunosuppressive therapy and before any surgical or endovascular intervention could be performed. Conclusions: This rare observation supports the role of immunosuppressive therapy in preventing the recurrence of lifethreatening vascular lesions in the management of Behcet's disease.