Pub Date : 2022-09-30eCollection Date: 2022-01-01DOI: 10.1055/s-0042-1756299
Shengliang He, Staci Beamer, Dawn Jaroszewski, Jonathan D'Cunha, Samine Ravanbakhsh
Background Lung cancer screening programs have increased the detection of early-stage lung cancer. High-resolution computed tomography can detect small, low-density pulmonary nodules, or ground-glass opacities. Obtaining a tissue diagnosis can be challenging, often necessitating surgical diagnosis. Preoperative localization and intraoperative fluoroscopy are valuable tools to guide resections for small pulmonary nodules. Case Description We present three cases using intraoperative fluoroscopy and Faxitron Bioptics that enhanced our certainty of resection of nonpalpable nodules. Conclusion We support the use of intraoperative fluoroscopy with the unique addition of Faxitron BioVision as safe and reliable methods to enhance the certainty of resection.
{"title":"A Simple Method to Improve Intraoperative Localization of Fiducial Markers during Lung Resections.","authors":"Shengliang He, Staci Beamer, Dawn Jaroszewski, Jonathan D'Cunha, Samine Ravanbakhsh","doi":"10.1055/s-0042-1756299","DOIUrl":"https://doi.org/10.1055/s-0042-1756299","url":null,"abstract":"<p><p><b>Background</b> Lung cancer screening programs have increased the detection of early-stage lung cancer. High-resolution computed tomography can detect small, low-density pulmonary nodules, or ground-glass opacities. Obtaining a tissue diagnosis can be challenging, often necessitating surgical diagnosis. Preoperative localization and intraoperative fluoroscopy are valuable tools to guide resections for small pulmonary nodules. <b>Case Description</b> We present three cases using intraoperative fluoroscopy and Faxitron Bioptics that enhanced our certainty of resection of nonpalpable nodules. <b>Conclusion</b> We support the use of intraoperative fluoroscopy with the unique addition of Faxitron BioVision as safe and reliable methods to enhance the certainty of resection.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e58-e60"},"PeriodicalIF":0.3,"publicationDate":"2022-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525182/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40390900","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}
Pub Date : 2022-07-19eCollection Date: 2022-01-01DOI: 10.1055/s-0042-1749140
Presheet Pathare, Michael Weyand, Christian Heim
Background Myxomas are the most common primary cardiac tumor in adults and are most commonly found within the left atrium. These are usually asymptomatic, detected incidentally, or present gradually with symptoms typical of heart failure. Case Description This case report is a description of a case of syncope caused by a large left atrial myxoma. Conclusion Atrial myxomas may present with transient loss of consciousness, especially when they prolapse through the atrioventricular valves or when embolization occurs. Non-invasive diagnostic tools (e.g., echocardiogram, cardiac computed tomography) should be considered to thoroughly evaluate cardiogenic causes of syncope.
{"title":"Prolapsing Left Atrial Mass Presenting as Syncope.","authors":"Presheet Pathare, Michael Weyand, Christian Heim","doi":"10.1055/s-0042-1749140","DOIUrl":"https://doi.org/10.1055/s-0042-1749140","url":null,"abstract":"<p><p><b>Background</b> Myxomas are the most common primary cardiac tumor in adults and are most commonly found within the left atrium. These are usually asymptomatic, detected incidentally, or present gradually with symptoms typical of heart failure. <b>Case Description</b> This case report is a description of a case of syncope caused by a large left atrial myxoma. <b>Conclusion</b> Atrial myxomas may present with transient loss of consciousness, especially when they prolapse through the atrioventricular valves or when embolization occurs. Non-invasive diagnostic tools (e.g., echocardiogram, cardiac computed tomography) should be considered to thoroughly evaluate cardiogenic causes of syncope.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e44-e46"},"PeriodicalIF":0.3,"publicationDate":"2022-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9296267/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40528843","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}
Pub Date : 2022-07-19eCollection Date: 2022-01-01DOI: 10.1055/s-0042-1750408
Jan Michael Federspiel, Thomas Tschernig, Matthias Werner Laschke, Hans-Joachim Schäfers
Background Quadricuspid aortic valve is rare and occasionally associated with aortic regurgitation and ascending aortic dilatation. Recent studies suggest an association of aortic regurgitation with ascending aortic medial degeneration. Case Description Histologic evaluation of ascending aortic tissue of two individuals with regurgitant quadricuspid aortic valve, one dilated, one non-dilated, yielded comparable degeneration in the Media. Conclusion Regurgitation of quadricuspid aortic valve may lead to the degeneration of Tunica media of the ascending aorta.
{"title":"Two Cases of Quadricuspid Aortic Valve: Aortic Regurgitation and Degeneration.","authors":"Jan Michael Federspiel, Thomas Tschernig, Matthias Werner Laschke, Hans-Joachim Schäfers","doi":"10.1055/s-0042-1750408","DOIUrl":"https://doi.org/10.1055/s-0042-1750408","url":null,"abstract":"<p><p><b>Background</b> Quadricuspid aortic valve is rare and occasionally associated with aortic regurgitation and ascending aortic dilatation. Recent studies suggest an association of aortic regurgitation with ascending aortic medial degeneration. <b>Case Description</b> Histologic evaluation of ascending aortic tissue of two individuals with regurgitant quadricuspid aortic valve, one dilated, one non-dilated, yielded comparable degeneration in the Media. <b>Conclusion</b> Regurgitation of quadricuspid aortic valve may lead to the degeneration of Tunica media of the ascending aorta.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e39-e43"},"PeriodicalIF":0.3,"publicationDate":"2022-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9296265/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40528907","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}
Pub Date : 2022-07-04eCollection Date: 2022-01-01DOI: 10.1055/s-0042-1746427
Teruhiko Imamura
{"title":"Clinical Course During LVAD Support in a Patient with Ventricular Pseudoaneurysm.","authors":"Teruhiko Imamura","doi":"10.1055/s-0042-1746427","DOIUrl":"https://doi.org/10.1055/s-0042-1746427","url":null,"abstract":"","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e38"},"PeriodicalIF":0.3,"publicationDate":"2022-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252610/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40476209","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}
Pub Date : 2022-07-04eCollection Date: 2022-01-01DOI: 10.1055/s-0042-1749211
Maximilian Vondran, Tamer Ghazy, Terézia Bogdana Andrási, Ardawan Julian Rastan
Background Cardiac myxoma is the most common primary cardiac tumor. Although benign, it can cause life-threatening complications due to embolization. Case Presentation We describe an ST-elevation myocardial infarction (STEMI) involving a giant right atrial myxoma and persisting foramen ovale (PFO) in a 64-year-old male patient and report on emergency percutaneous interventional therapy and subsequent cardiac surgery to remove the right atrial myxoma. Conclusion A right atrial myxoma, combined with a PFO, can cause a STEMI. Therefore, every acute coronary syndrome patient should undergo ultrafast exploratory emergency echocardiography to protect the physician from unpleasant surprises.
{"title":"ST-Segment Elevation Myocardial Infarction and Right Atrial Myxoma.","authors":"Maximilian Vondran, Tamer Ghazy, Terézia Bogdana Andrási, Ardawan Julian Rastan","doi":"10.1055/s-0042-1749211","DOIUrl":"https://doi.org/10.1055/s-0042-1749211","url":null,"abstract":"<p><p><b>Background</b> Cardiac myxoma is the most common primary cardiac tumor. Although benign, it can cause life-threatening complications due to embolization. <b>Case Presentation</b> We describe an ST-elevation myocardial infarction (STEMI) involving a giant right atrial myxoma and persisting foramen ovale (PFO) in a 64-year-old male patient and report on emergency percutaneous interventional therapy and subsequent cardiac surgery to remove the right atrial myxoma. <b>Conclusion</b> A right atrial myxoma, combined with a PFO, can cause a STEMI. Therefore, every acute coronary syndrome patient should undergo ultrafast exploratory emergency echocardiography to protect the physician from unpleasant surprises.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e33-e37"},"PeriodicalIF":0.3,"publicationDate":"2022-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252612/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40476208","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}
Pub Date : 2022-06-25eCollection Date: 2022-01-01DOI: 10.1055/s-0042-1750427
Xijie Gao, Guohong Liu, Jun Lu, Jianbo Zhao
Background The management of aortic lesions involving the aortic arch in patients who cannot tolerate thoracotomy is a challenge. Case Description A 32-year-old woman who underwent a giant aneurysm at the proximal end of the descending aorta with significant vascular wall calcification. The patient underwent Castor single-branched stent-grafting in the brachiocephalic trunk combined with surgical supra-aortic debranching, which avoided surgical aortic arch replacement and stent fenestration.reopening. The patient was followed up for 9 months, and surgery-related complications were not observed. Conclusion Hybrid arch repair with supra-aortic debranching and using Castor single-branched stent can be used to treat aortic lesions involving the aortic arch.
{"title":"Hybrid Arch Repair with Supra-Aortic Debranching and Using Castor Stent-Graft.","authors":"Xijie Gao, Guohong Liu, Jun Lu, Jianbo Zhao","doi":"10.1055/s-0042-1750427","DOIUrl":"https://doi.org/10.1055/s-0042-1750427","url":null,"abstract":"<p><p><b>Background</b> The management of aortic lesions involving the aortic arch in patients who cannot tolerate thoracotomy is a challenge. <b>Case Description</b> A 32-year-old woman who underwent a giant aneurysm at the proximal end of the descending aorta with significant vascular wall calcification. The patient underwent Castor single-branched stent-grafting in the brachiocephalic trunk combined with surgical supra-aortic debranching, which avoided surgical aortic arch replacement and stent fenestration.reopening. The patient was followed up for 9 months, and surgery-related complications were not observed. <b>Conclusion</b> Hybrid arch repair with supra-aortic debranching and using Castor single-branched stent can be used to treat aortic lesions involving the aortic arch.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e30-e32"},"PeriodicalIF":0.3,"publicationDate":"2022-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233568/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40401372","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}
Pub Date : 2021-12-31eCollection Date: 2021-01-01DOI: 10.1055/s-0041-1731275
Haval Sadraddin, Ulrich Krüger, Jochen Börgermann, Mustafa Gerçek
Our report presents a 73-year-old female patient with severe aortic stenosis who was admitted to our department for a surgical aortic valve replacement. After an uneventful surgery, a worsening low cardiac output syndrome with signs of myocardial ischemia occurred. Immediate angiography revealed a diffuse left coronary dissection starting from the ostium extending to the periphery of the left coronary system. The diffuse nature of the dissection ruled interventional management out and thus has been treated with urgent coronary bypass surgery. However, after an antecedent favorable course, the patient died 2 months later due to pneumonia resulting in septic shock.
{"title":"Dissection of the Left Coronary Artery after Surgical Aortic Valve Replacement.","authors":"Haval Sadraddin, Ulrich Krüger, Jochen Börgermann, Mustafa Gerçek","doi":"10.1055/s-0041-1731275","DOIUrl":"https://doi.org/10.1055/s-0041-1731275","url":null,"abstract":"<p><p>Our report presents a 73-year-old female patient with severe aortic stenosis who was admitted to our department for a surgical aortic valve replacement. After an uneventful surgery, a worsening low cardiac output syndrome with signs of myocardial ischemia occurred. Immediate angiography revealed a diffuse left coronary dissection starting from the ostium extending to the periphery of the left coronary system. The diffuse nature of the dissection ruled interventional management out and thus has been treated with urgent coronary bypass surgery. However, after an antecedent favorable course, the patient died 2 months later due to pneumonia resulting in septic shock.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e52-e54"},"PeriodicalIF":0.3,"publicationDate":"2021-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720027/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39662310","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}
Pub Date : 2021-12-25eCollection Date: 2021-01-01DOI: 10.1055/s-0041-1736208
Philipp P Müller, Abbas Agaimy, Michael Weyand, Christian Heim
Mitral valve fibroelastoma is a rare condition that can be associated with high morbidity rates due to thrombus formation and resulting embolic events. Causative treatment for affected patients is mitral valve surgery. An association between cardiac fibroelastoma and desmoid-type fibromatosis, an aggressive form of fibromatosis, is not yet described. We present a case of a 58-year-old man with a history of desmoid-type fibromatosis and concomitant papillary fibroelastoma of the mitral valve who consequently underwent mitral valve replacement.
{"title":"Mitral Multifocal Papillary Fibroelastoma in a Patient with Aggressive Fibromatosis.","authors":"Philipp P Müller, Abbas Agaimy, Michael Weyand, Christian Heim","doi":"10.1055/s-0041-1736208","DOIUrl":"https://doi.org/10.1055/s-0041-1736208","url":null,"abstract":"<p><p>Mitral valve fibroelastoma is a rare condition that can be associated with high morbidity rates due to thrombus formation and resulting embolic events. Causative treatment for affected patients is mitral valve surgery. An association between cardiac fibroelastoma and desmoid-type fibromatosis, an aggressive form of fibromatosis, is not yet described. We present a case of a 58-year-old man with a history of desmoid-type fibromatosis and concomitant papillary fibroelastoma of the mitral valve who consequently underwent mitral valve replacement.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e61-e63"},"PeriodicalIF":0.3,"publicationDate":"2021-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8710145/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39885026","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}
Pub Date : 2021-11-10eCollection Date: 2021-01-01DOI: 10.1055/s-0041-1735478
Geoffrey Jacqmin, Manuel Pirotte, Carlo Caravaggio, Philippe Devaux
Background Spontaneous pneumomediastinum (SP) is the presence of free air into extra-alveolar tissues within the mediastinum, without notion of trauma. This rare condition may occur as a complication of an underlying severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia. Higher rates of mechanical ventilation are reported in coronavirus disease 2019 (COVID-19) patients with pneumomediastinum. Case Description We report two cases of COVID-19 infected patients suffering from mild and severe SP and their outcome. Discussion The objective of this report is to review the literature about this condition. We discuss about the pathological pathways underlying this complication and how it reflects the severity of COVID-19 pneumonia. Conclusion Currently, it remains unclear if SP in SARS-CoV-2 pneumonia is a potential predictor of disease worsening, for it does not seem to be related with a higher rate of mortality.
{"title":"Spontaneous Pneumomediastinum: A Possible Severe Condition in SARS-CoV-2 Pneumonia.","authors":"Geoffrey Jacqmin, Manuel Pirotte, Carlo Caravaggio, Philippe Devaux","doi":"10.1055/s-0041-1735478","DOIUrl":"https://doi.org/10.1055/s-0041-1735478","url":null,"abstract":"<p><p><b>Background</b> Spontaneous pneumomediastinum (SP) is the presence of free air into extra-alveolar tissues within the mediastinum, without notion of trauma. This rare condition may occur as a complication of an underlying severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia. Higher rates of mechanical ventilation are reported in coronavirus disease 2019 (COVID-19) patients with pneumomediastinum. <b>Case Description</b> We report two cases of COVID-19 infected patients suffering from mild and severe SP and their outcome. <b>Discussion</b> The objective of this report is to review the literature about this condition. We discuss about the pathological pathways underlying this complication and how it reflects the severity of COVID-19 pneumonia. <b>Conclusion</b> Currently, it remains unclear if SP in SARS-CoV-2 pneumonia is a potential predictor of disease worsening, for it does not seem to be related with a higher rate of mortality.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e55-e58"},"PeriodicalIF":0.3,"publicationDate":"2021-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580730/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39732083","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}
Pub Date : 2021-11-10eCollection Date: 2021-01-01DOI: 10.1055/s-0041-1732344
Katharina Huenges, Philipp Kolat, Bernd Panholzer, Assad Haneya
Background Posterior reversible encephalopathy syndrome (PRES) is a rare neurological disease possibly associated with the use of calcineurin inhibitors (CNI) like cyclosporine A. Case Description The case of a patient who developed severe PRES under CNI therapy shortly after heart transplantation is presented here. Cerebral computed tomography led to the diagnose of PRES in our patient. New therapy strategy with a quadruple immunosuppressive protocol (cortisone, mycophenolate mofetil, low-dose CNI, and a mechanistic target of rapamycin inhibitor) was started. Conclusion Under the quadruple therapy, a neurologic recovery occurred. In PRES, the presented alternative therapy strategy may lead to improving neurological conditions and preserved transplant organ functions.
{"title":"CSA-Induced PRES after Heart Transplantation-Report of Two Cases and Review.","authors":"Katharina Huenges, Philipp Kolat, Bernd Panholzer, Assad Haneya","doi":"10.1055/s-0041-1732344","DOIUrl":"https://doi.org/10.1055/s-0041-1732344","url":null,"abstract":"<p><p><b>Background</b> Posterior reversible encephalopathy syndrome (PRES) is a rare neurological disease possibly associated with the use of calcineurin inhibitors (CNI) like cyclosporine A. <b>Case Description</b> The case of a patient who developed severe PRES under CNI therapy shortly after heart transplantation is presented here. Cerebral computed tomography led to the diagnose of PRES in our patient. New therapy strategy with a quadruple immunosuppressive protocol (cortisone, mycophenolate mofetil, low-dose CNI, and a mechanistic target of rapamycin inhibitor) was started. <b>Conclusion</b> Under the quadruple therapy, a neurologic recovery occurred. In PRES, the presented alternative therapy strategy may lead to improving neurological conditions and preserved transplant organ functions.</p>","PeriodicalId":41729,"journal":{"name":"Thoracic and Cardiovascular Surgeon Reports","volume":" ","pages":"e59-e60"},"PeriodicalIF":0.3,"publicationDate":"2021-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580731/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39732084","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}