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Mitral Annular Calcification in Marfan Syndrome: A 38-Year Follow-Up Observation. 马凡氏综合征二尖瓣环钙化:38年随访观察。
IF 0.3
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2021-01-01 Epub Date: 2021-08-28 DOI: 10.1055/s-0041-1728720
Kazutaka Horiuchi
{"title":"Mitral Annular Calcification in Marfan Syndrome: A 38-Year Follow-Up Observation.","authors":"Kazutaka Horiuchi","doi":"10.1055/s-0041-1728720","DOIUrl":"https://doi.org/10.1055/s-0041-1728720","url":null,"abstract":"<p><p><b>Background</b>  Mitral annular calcification (MAC) associated with Marfan syndrome is rare in comparison with that frequently found in elderlies with valvular disease. <b>Case Presentation</b>  A 17-year-old woman with Marfan syndrome underwent mitral valve replacement for severe mitral regurgitation. Preoperative examination showed mitral valve prolapse and a dense C -shaped MAC. We evaluated MAC and adjacent area, respectively, in postoperative 18 and 38 years, and neither progression nor expansion of calcification was observed. <b>Conclusion</b>  MAC associated with Marfan syndrome is more likely to be caused by stresses due to valve prolapse than by connective tissue disorder.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e49-e51"},"PeriodicalIF":0.3,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403017/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39388347","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Management of a Residual VSD 60 Years after One of the First Operations Worldwide. 全球首次手术 60 年后的残留 VSD 管理。
IF 0.3
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2021-01-01 Epub Date: 2021-03-19 DOI: 10.1055/s-0040-1722734
Yasser Yehia Hegazy, Mohamed Koriem, Noha Samir Keshk-Hegazy, Ralf Sodian
{"title":"Management of a Residual VSD 60 Years after One of the First Operations Worldwide.","authors":"Yasser Yehia Hegazy, Mohamed Koriem, Noha Samir Keshk-Hegazy, Ralf Sodian","doi":"10.1055/s-0040-1722734","DOIUrl":"10.1055/s-0040-1722734","url":null,"abstract":"<p><p><b>Background</b>  Although surgical closure of ventricular septal defect (VSD) is the gold standard treatment, patients are subjected to deterioration in the following decades. We will present here the first case in literature surviving 60 years after surgical VSD closure with a residual VSD and presenting again for surgery. <b>Case Description</b>  A 68-year-old male patient who underwent surgical closure of a perimembranous VSD in Berlin in 1959. Postoperatively, a small residual VSD was noticed, which was well tolerated over six decades. He presented 60 years postoperatively with severe aortic regurgitation, tricuspid regurgitation, and moderate mitral regurgitation.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e22-e24"},"PeriodicalIF":0.3,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979319/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25512346","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Continuing Education through COVID-19 Crisis in the United Kingdom: A Swiss Trainee Abroad. 新冠肺炎危机下的英国继续教育:一名瑞士海外实习生。
IF 0.3
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2021-01-01 Epub Date: 2021-03-19 DOI: 10.1055/s-0040-1722708
Alicja Zientara
{"title":"Continuing Education through COVID-19 Crisis in the United Kingdom: A Swiss Trainee Abroad.","authors":"Alicja Zientara","doi":"10.1055/s-0040-1722708","DOIUrl":"https://doi.org/10.1055/s-0040-1722708","url":null,"abstract":"<p><p>The work has been awarded in July 2020 with the \"Special Swiss Young Cardiac Surgeon Award 2020\" by the Swiss Society of Cardiac Surgery (Schweizerische Gesellschaft für Herz- und thorakale Gefässchirurgie [SGHC-SSCC]) and reflects a personal perspective from a Swiss trainee experiencing the novel coronavirus disease 2019 (COVID-19) pandemic during her fellowship in London.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e25-e29"},"PeriodicalIF":0.3,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0040-1722708","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25512347","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acute Type A Dissection during Pregnancy with Marfan's Syndrome. 妊娠期急性A型夹层与马凡氏综合征。
IF 0.3
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2021-01-01 Epub Date: 2021-03-11 DOI: 10.1055/s-0040-1722705
Christian Heim, Philipp P Müller, Michael Weyand, Frank Harig
{"title":"Acute Type A Dissection during Pregnancy with Marfan's Syndrome.","authors":"Christian Heim,&nbsp;Philipp P Müller,&nbsp;Michael Weyand,&nbsp;Frank Harig","doi":"10.1055/s-0040-1722705","DOIUrl":"https://doi.org/10.1055/s-0040-1722705","url":null,"abstract":"<p><p><b>Background</b>  Marfan's syndrome (MFS) is a connective tissue disorder, caused by a mutation in the <i>FBN-1</i> gene and affecting multiple organ systems including the vascular system. During pregnancy, women with MFS have an increased risk of aortic dissection due to changes in the cardiovascular system. <b>Case Description</b>  We present a 39-year-old woman that suffered from an acute aortic dissection in week 33 of her third pregnancy who urgently required lifesaving surgery. Three-dimensional reconstruction of computed tomography scan was performed with unborn child in utero. <b>Conclusion</b>  Monitoring of patients with suspected or confirmed MFS appears essential and interdisciplinary treatment and prevention strategies are required.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e18-e21"},"PeriodicalIF":0.3,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0040-1722705","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25477100","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Black Aortic Valve: Incidental Finding of Alkaptonuria. 黑色主动脉瓣:尿酸尿的偶然发现。
IF 0.3
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2021-01-01 Epub Date: 2021-06-27 DOI: 10.1055/s-0041-1728721
Christina Putz, Franz Josef Putz, Andreas Keyser, Christof Schmid
{"title":"Black Aortic Valve: Incidental Finding of Alkaptonuria.","authors":"Christina Putz,&nbsp;Franz Josef Putz,&nbsp;Andreas Keyser,&nbsp;Christof Schmid","doi":"10.1055/s-0041-1728721","DOIUrl":"https://doi.org/10.1055/s-0041-1728721","url":null,"abstract":"<p><p><b>Background</b>  Alkaptonuria is a rare autosomal recessive genetic disorder of tyrosine metabolism, which results in accumulation of homogentisic acid in various tissues, including the cardiovascular system. <b>Case Description</b>  We report on a 64-year-old man with mixed aortic valve disease who underwent conventional aortic valve replacement. Intraoperative aortotomy revealed black pigmentation of the intima of the ascending aorta and the aortic valve was observed with thickened and calcified dark black leaflets. Histopathological diagnosis of ochronosis of the aortic valve was made. <b>Conclusion</b>  Despite several previous signs and symptoms, the diagnosis of alkaptonuria was not established until aortic valve replacement.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e39-e41"},"PeriodicalIF":0.3,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0041-1728721","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39058199","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Robotic Resection of Pulmonary Epithelial Myoepithelial Carcinoma: A Case Report. 机器人切除肺上皮性肌上皮癌1例报告。
IF 0.3
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2021-01-01 Epub Date: 2021-06-27 DOI: 10.1055/s-0041-1723836
Rajika Jindani, Michael A Lopez, Tatiana P Miquel, Erik Sylvin
{"title":"Robotic Resection of Pulmonary Epithelial Myoepithelial Carcinoma: A Case Report.","authors":"Rajika Jindani,&nbsp;Michael A Lopez,&nbsp;Tatiana P Miquel,&nbsp;Erik Sylvin","doi":"10.1055/s-0041-1723836","DOIUrl":"https://doi.org/10.1055/s-0041-1723836","url":null,"abstract":"<p><p><b>Background</b>  Pulmonary epithelial-myoepithelial carcinoma (P-EMC) is an extremely rare, well-differentiated, and malignant neoplasm originating from submucosal bronchial glands in the lung. EMCs arise mainly in the salivary glands. <b>Case Description</b>  This case represents an asymptomatic 78-year-old male with a remote 75-pack-year history of smoking who presents with a solitary endobronchial lesion, which is suggestive of a primary lung EMC, detected on annual screening chest computed tomography (CT) scan. <b>Conclusion</b>  A recent review of literature reveals less than 50 documented cases of the pulmonary subtype of this tumor worldwide. We are reporting a unique case of robot-assisted pulmonary lobectomy for a P-EMC.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e42-e44"},"PeriodicalIF":0.3,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0041-1723836","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39058200","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Allegra Transcatheter Heart Valve inside a Degenerated Sutureless Aortic Bioprosthesis. 阿利格拉经导管心脏瓣膜内退化无缝合主动脉生物假体。
IF 0.3
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2021-01-01 Epub Date: 2021-01-19 DOI: 10.1055/s-0040-1721483
Maximilian Vondran, Bernd Abt, Holger Nef, Ardawan J Rastan
{"title":"Allegra Transcatheter Heart Valve inside a Degenerated Sutureless Aortic Bioprosthesis.","authors":"Maximilian Vondran,&nbsp;Bernd Abt,&nbsp;Holger Nef,&nbsp;Ardawan J Rastan","doi":"10.1055/s-0040-1721483","DOIUrl":"https://doi.org/10.1055/s-0040-1721483","url":null,"abstract":"<p><p>Transcatheter aortic valve-in-valve implantation (VIV) is increasingly being used to successfully treat degenerated surgical aortic valve bioprostheses (SAVs). The new self-expanding transcatheter heart valve Allegra, from New Valve Technology with its special implantation mechanism, has proven its safety and feasibility for patients with degenerated SAVs, but it has never been used in the latest-generation sutureless SAV. To the best of our knowledge, this is the first description of the successful VIV of the Allegra prosthesis into a degenerated sutureless SAV, and the procedure yielded an excellent postinterventional hemodynamic results.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e1-e5"},"PeriodicalIF":0.3,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0040-1721483","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38856415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Anomalous Origin of the Left Anterior Descending Coronary Artery in an Adult. 成人左冠状动脉前降支异常起源。
IF 0.3
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2021-01-01 Epub Date: 2021-01-19 DOI: 10.1055/s-0040-1721470
Keisuke Shibagaki, Chikara Shiiku, Hiroyuki Kamiya, Yoichi Kikuchi
{"title":"Anomalous Origin of the Left Anterior Descending Coronary Artery in an Adult.","authors":"Keisuke Shibagaki,&nbsp;Chikara Shiiku,&nbsp;Hiroyuki Kamiya,&nbsp;Yoichi Kikuchi","doi":"10.1055/s-0040-1721470","DOIUrl":"https://doi.org/10.1055/s-0040-1721470","url":null,"abstract":"<p><p>An anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital heart disease. Among the variants, an anomalous origin of the left anterior descending coronary artery from the pulmonary artery (ALADPA) is extremely rare. Here, we report a case of ALADPA in an adult that was treated with coronary artery bypass grafting using the left internal thoracic artery.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e9-e10"},"PeriodicalIF":0.3,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0040-1721470","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38856417","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Management of Leukemia and Partial Atrioventricular Septal Defect during Pregnancy. 妊娠期白血病和部分房室间隔缺损的处理。
IF 0.3
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2021-01-01 Epub Date: 2021-06-28 DOI: 10.1055/s-0041-1722876
Zhi Li, Haoliang Sun, Jinghang Li, Yu Zhu
{"title":"Management of Leukemia and Partial Atrioventricular Septal Defect during Pregnancy.","authors":"Zhi Li,&nbsp;Haoliang Sun,&nbsp;Jinghang Li,&nbsp;Yu Zhu","doi":"10.1055/s-0041-1722876","DOIUrl":"https://doi.org/10.1055/s-0041-1722876","url":null,"abstract":"<p><p><b>Background</b>  Pregnancy-associated acute myeloid leukemia (PA-AML) is rare. Cardiac surgery in the context of AML poses challenges that are seldom encountered. <b>Case Description</b>  The subject is a 31-year-old woman at 38 weeks' gestational age diagnosed with AML and partial atrioventricular septal defect. After multidisciplinary consulting, an urgent cesarean section was performed, then chemotherapy was initiated, followed by minimally invasive cardiac surgery with an uneventful recovery. <b>Conclusion</b>  Efficient multidisciplinary approach is essential in the management of PA-AML and cardiac disease. Minimally invasive cardiac surgery may be safe and useful in patients with AML.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e45-e48"},"PeriodicalIF":0.3,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0041-1722876","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39142203","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
COVID-19 Pandemic-What Should Not Be Forgotten. COVID-19 大流行病--不应忘记的事情。
IF 0.3
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2021-01-01 Epub Date: 2021-04-20 DOI: 10.1055/s-0040-1721024
Luca Koechlin
{"title":"COVID-19 Pandemic-What Should Not Be Forgotten.","authors":"Luca Koechlin","doi":"10.1055/s-0040-1721024","DOIUrl":"10.1055/s-0040-1721024","url":null,"abstract":"<p><p>The Swiss Society of Cardiac Surgery (SGHC) has announced a \"Special Swiss Young Cardiac Surgeon Award 2020,\" with the aim to learn more about the consequences of the coronavirus disease 2019 (COVID-19) pandemic for young Swiss cardiac surgeons. Therefore, the overall goal of this article is to highlight the personal situation and perspective of a young Swiss cardiac surgeon in training during the COVID-19 pandemic. This article reflects the personal opinion of a young Swiss cardiac surgeon discussing the impact of the pandemic for young surgeons in training and potential chances and learning effects.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e31-e35"},"PeriodicalIF":0.3,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8057867/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38834007","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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