Case Reports in Cardiology最新文献_第2页

Successful Retrieval of Rota Burr After Driveshaft Fracture. 传动轴断裂后成功取出 Rota Burr。

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Case Reports in Cardiology Pub Date : 2024-06-17 eCollection Date: 2024-01-01 DOI: 10.1155/2024/5482922

Tsuyoshi Kobayashi, Takeo Horikoshi, Toru Yoshizaki, Akira Sato

引用次数: 0

Leveraging Color M-Mode to Diagnose Aorto-Atrial Fistula as a Complication of Infective Endocarditis. 利用彩色 M-Mode 诊断感染性心内膜炎并发的主动脉-心房瘘

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Case Reports in Cardiology Pub Date : 2024-05-25 eCollection Date: 2024-01-01 DOI: 10.1155/2024/7550403

Kramer J Wahlberg, Matthew A Kluge, William E Hopkins

引用次数: 0

Rare Manifestation of COVID-19 Resulting in Coronary Artery Vasculitis. COVID-19导致冠状动脉血管炎的罕见表现。

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Case Reports in Cardiology Pub Date : 2024-01-30 eCollection Date: 2024-01-01 DOI: 10.1155/2024/8976833

Ahmed Hassaan Qavi, Soban Ahmad, Neeraj N Shah, Rony Shammas

引用次数: 0

Heart Failure in a Young Adult with a Fine-Lubinsky Syndrome: An Unknown Comorbidity 患有 Fine-Lubinsky 综合征的年轻成人的心力衰竭：一种未知的并发症

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Case Reports in Cardiology Pub Date : 2024-01-02 DOI: 10.1155/2024/5596010

Blake Purtle, Jason Wagner, Andrew Zarker, Vishal Patel, David Aguilar

引用次数: 0

Pacemaker Lead Entanglement during Interventional PFO Occlusion: Salvage Using a Sizing Balloon. 介入性 PFO 闭塞时起搏器导线缠绕：使用定径球囊进行抢救

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Case Reports in Cardiology Pub Date : 2023-12-13 eCollection Date: 2023-01-01 DOI: 10.1155/2023/5586197

Andreas Goldschmied, Juergen Schreieck, Michal Droppa

引用次数: 0

Recurrent Biatrial Myxomas in Carney Complex with a Spinal Melanotic Schwannoma: Advocacy for a Rigorous Multidisciplinary Follow-Up. 患有脊髓黑色素性许旺瘤的卡尼复合体复发性双房肌瘤：倡导严格的多学科随访。

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Case Reports in Cardiology Pub Date : 2023-12-11 eCollection Date: 2023-01-01 DOI: 10.1155/2023/7896180

Daniel Grandmougin, Teresa Moussu, Maxime Hubert, Benjamin Perin, Arthur Huber, Maria Christina Delolme, Juan-Pablo Maureira

{"title":"Recurrent Biatrial Myxomas in Carney Complex with a Spinal Melanotic Schwannoma: Advocacy for a Rigorous Multidisciplinary Follow-Up.","authors":"Daniel Grandmougin, Teresa Moussu, Maxime Hubert, Benjamin Perin, Arthur Huber, Maria Christina Delolme, Juan-Pablo Maureira","doi":"10.1155/2023/7896180","DOIUrl":"10.1155/2023/7896180","url":null,"abstract":"A 31-year-old female patient with a previous history of Carney complex and surgical resection for cardiac myxoma and bilateral adrenalectomy at 18 years old and 10 and 11 years old, respectively, was referred to our department with a diagnosis of recurrent biatrial myxomas incidentally discovered on echography. A magnetic resonance imaging (MRI) confirmed the diagnosis of a tumor protruding into the left ventricle, and the patient underwent a surgical resection of a large left atrial mass and a right-sided atrial small tumor. Diagnosis of bilateral atrial myxomas was confirmed by histologic studies. Postoperative outcome was uneventful, and the patient was discharged at the 7th postoperative day. Few months later, she reported trivial clinical symptoms suspecting a cervical radiculopathy. MRI confirmed the presence of a compressive cervical spinal cord tumoral mass at the C2-3 level leading to perform a surgical exeresis of the tumor. Histology showed a spinal melanotic schwannoma. This case highlights the risk of unexpected ubiquitary tumor locations and the importance of a rigorous transversal multidisciplinary follow-up to prevent severe complications in patients with Carney complex.","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"7896180"},"PeriodicalIF":0.6,"publicationDate":"2023-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10728359/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138811198","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

An Unusual Presentation of Streptococcus gallolyticus in Infective Endocarditis. 感染性心内膜炎胆溶血性链球菌的异常表现

IF 0.6

Case Reports in Cardiology Pub Date : 2023-11-30 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9948719

Laura Torres Cruz, Maryam Barkhordarian, Neenu Antony, Muhammad Yasir, Sai Priyanka Pulipaka, Ahmad Al-Awwa, Sameh Elias

{"title":"An Unusual Presentation of Streptococcus gallolyticus in Infective Endocarditis.","authors":"Laura Torres Cruz, Maryam Barkhordarian, Neenu Antony, Muhammad Yasir, Sai Priyanka Pulipaka, Ahmad Al-Awwa, Sameh Elias","doi":"10.1155/2023/9948719","DOIUrl":"https://doi.org/10.1155/2023/9948719","url":null,"abstract":"Background. Streptococcus gallolyticus (previously known as Streptococcus bovis type-1) bacteremia has a well-established, almost pathognomonic association with colorectal carcinoma, with the most common hypothesized mechanism being ulceration of polyps leading to hematologic dissemination. There are few reported cases of streptococcus bacteremia from other, seemingly benign sources like cellulitis or colonic adenomas. Hence, there is limited focus on skin and soft tissue infections leading to potentially fatal infective endocarditis. Case Presentation. We present a novel case of streptococcus bacteremia from uncommon sources like abdominal wall cellulitis or colonic adenoma leading to infective endocarditis as well as other manifestations, including osteomyelitis and discitis. This report highlights a unique case of streptococcus bacteremia with an uncommon origin, arising from abdominal wall cellulitis or colonic adenoma, ultimately resulting in the development of infective endocarditis. Furthermore, the patient presented with additional clinical manifestations, including osteomyelitis and discitis. Conclusions. Through our case report, we emphasize the importance of investigating uncommon sources like cellulitis when initial malignant workup is negative in streptococcus bacteremia and further elucidate the pathophysiology of streptococcus bacterial dissemination from nonmalignancy-related sources.","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"9948719"},"PeriodicalIF":0.6,"publicationDate":"2023-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10703536/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138811113","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

IgG4-Related Pericarditis Diagnosed by Accumulated Pericardial Effusion. 积液诊断igg4相关性心包炎。

IF 0.6

Case Reports in Cardiology Pub Date : 2023-11-24 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9223342

Hirohito Sugawara, Tomokazu Takahashi, Yukishige Kimura, Azumi Matsui, Tamaki Matsumoto, Kimio Nishisato, Mitsuhiro Nishimura

引用次数: 0

Aortic Pseudoaneurysm following Ventricular Septal Defect Closure in a Pediatric Patient: A Case Report and Literature Review. 小儿室间隔缺损闭合后主动脉假性动脉瘤1例报告及文献回顾。

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Case Reports in Cardiology Pub Date : 2023-11-23 eCollection Date: 2023-01-01 DOI: 10.1155/2023/2890844

Hassan Zamani, Kourosh Vahidshahi, Mohammad Reza Khalilian, Tahmineh Tahouri, Ehsanollah Rahimi-Movaghar

{"title":"Aortic Pseudoaneurysm following Ventricular Septal Defect Closure in a Pediatric Patient: A Case Report and Literature Review.","authors":"Hassan Zamani, Kourosh Vahidshahi, Mohammad Reza Khalilian, Tahmineh Tahouri, Ehsanollah Rahimi-Movaghar","doi":"10.1155/2023/2890844","DOIUrl":"10.1155/2023/2890844","url":null,"abstract":"Aortic pseudoaneurysm, a rare condition characterized by localized transmural disruption and dilatation of the aorta, is very rare in the pediatric population. It is primarily caused by previous cardiovascular procedures such as aortic coarctation repair, aortic valve replacement, and subaortic membrane resection. We present a unique case of aortic pseudoaneurysm following surgery to repair a perimembranous ventricular septal defect in a 19-month-old boy who presented with fever as the sole symptom. The fever started on the 30th day after the surgery, and the patient exhibited abnormal laboratory results, including a white blood cell (WBC) count of 28.3 × 109/L, neutrophil percentage of 68%, platelet count of 880 × 109/L, erythrocyte sedimentation rate (ESR) of 200 mm/hour, and 3+ positive C-reactive protein. Echocardiogram revealed a large cystic mass (5 × 4.8 cm) in the ascending aorta, compressing the superior vena cava. Based on this finding, a diagnosis of aortic pseudoaneurysm was suspected. The diagnosis was confirmed through cardiac computed tomographic angiography, and the patient underwent emergent surgery for the repair of the aortic pseudoaneurysm under deep hypothermia and circulatory arrest. Unfortunately, our patient died shortly after the surgery.","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"2890844"},"PeriodicalIF":0.6,"publicationDate":"2023-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10689068/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138479269","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

To PLEX or Not to PLEX for Amiodarone-Induced Thyrotoxicosis. 胺碘酮性甲状腺毒症是否应用PLEX。

IF 0.6

Case Reports in Cardiology Pub Date : 2023-11-20 eCollection Date: 2023-01-01 DOI: 10.1155/2023/1563732

Tania Ahuja, Olivia Nuti, Cameron Kemal, Darren Kang, Eugene Yuriditsky, James M Horowitz, Raymond A Pashun

引用次数: 0