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Warning Function of Frank's Sign in Pre-Existing Cardiac Disease Patients: A Case Report. 先心病患者弗兰克体征的预警功能：病例报告
IF 0.6
Case Reports in Cardiology Pub Date : 2024-07-09 eCollection Date: 2024-01-01 DOI: 10.1155/2024/3766536
Mingzhe Wang, Yujing Zhang, Jiang Huang, Geping Liao, Wei Qian, Yaofu Zheng, Xiaoping Peng, Jianbing Zhu
{"title":"Warning Function of Frank's Sign in Pre-Existing Cardiac Disease Patients: A Case Report.","authors":"Mingzhe Wang, Yujing Zhang, Jiang Huang, Geping Liao, Wei Qian, Yaofu Zheng, Xiaoping Peng, Jianbing Zhu","doi":"10.1155/2024/3766536","DOIUrl":"10.1155/2024/3766536","url":null,"abstract":"<p><p>Frank's sign (FS) refers to a diagonal skin fold between the tragus and the outer edge of the earlobe. FS has been identified as an independent variable in coronary artery disease (CAD). Young patients with FS and previous myocardial infarction are still rarely reported in clinical studies. We report the case of a 49-year-old male smoker and diabetic, with a history of myocardial infarction, who presented to the emergency department due to 2 h typical cardiac chest pain. His urgent electrocardiography (ECG) showed ST elevation, and cardiac biomarkers were elevated after admission. A diagonal earlobe crease (DELC) was observed in physical tests. The preliminary diagnosis considered acute coronary syndrome (ACS). Subsequently, acute coronary artery angiography demonstrated a slit-like contrast defect in the proximal right coronary artery (RCA), with stenosis and occlusion in the distal segment. The percutaneous coronary intervention (PCI) was performed immediately. The patient's chest pain symptoms were relieved significantly after intervention. Our case indicates that FS should be highly regarded as a routine cardiovascular clinical examination, which can be effortlessly applied and be easily interpreted for screening to suspect the presence of ischemic heart disease. This may set strategies for primary screening in a younger population and prompt early diagnosis and treatment.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2024 ","pages":"3766536"},"PeriodicalIF":0.6,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11251791/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141629265","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
Left Pulmonary Artery Stenting for Left Pulmonary Artery Stenosis Following Patent Ductus Arteriosus Device Closure: Case Series and Review of the Literature. 左肺动脉支架植入术治疗动脉导管未闭装置闭合后左肺动脉狭窄：病例系列和文献综述。
IF 0.6
Case Reports in Cardiology Pub Date : 2024-06-24 eCollection Date: 2024-01-01 DOI: 10.1155/2024/6690515
Víctor Molina, Mehdi Hadid, Joaquim Miró, Nagib Dahdah
{"title":"Left Pulmonary Artery Stenting for Left Pulmonary Artery Stenosis Following Patent Ductus Arteriosus Device Closure: Case Series and Review of the Literature.","authors":"Víctor Molina, Mehdi Hadid, Joaquim Miró, Nagib Dahdah","doi":"10.1155/2024/6690515","DOIUrl":"10.1155/2024/6690515","url":null,"abstract":"<p><p>Percutaneous device occlusion is currently the standard of care for most cases of patent ductus arteriosus (PDA). Albeit infrequent, device-related left pulmonary artery (LPA) stenosis is a known complication of this procedure, occasionally requiring stent placement to relieve the obstruction. We present a series of four patients who required left pulmonary stenting after ductus arteriosus device closure. A review of the current evidence is presented.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2024 ","pages":"6690515"},"PeriodicalIF":0.6,"publicationDate":"2024-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11217573/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141494175","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
Successful Retrieval of Rota Burr After Driveshaft Fracture. 传动轴断裂后成功取出 Rota Burr。
IF 0.6
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
{"title":"Successful Retrieval of Rota Burr After Driveshaft Fracture.","authors":"Tsuyoshi Kobayashi, Takeo Horikoshi, Toru Yoshizaki, Akira Sato","doi":"10.1155/2024/5482922","DOIUrl":"10.1155/2024/5482922","url":null,"abstract":"<p><p>Rotational atherectomy is an effective procedure for heavily calcified lesions and those that cannot be crossed using conventional percutaneous coronary intervention (PCI) devices. Here, we report a rare case of intracoronary burr entrapment in the coronary artery due to burr disconnection from the driveshaft. A 67-year-old man undergoing hemodialysis for nephrosclerosis presented with exertional chest discomfort. Coronary angiography revealed stenotic lesions in the right coronary artery, and PCI was performed using a Rotawire Floppy. During the procedure, the disconnected burr was successfully removed without surgery using the child-in-mother technique with a guide extension catheter. Notably, the patient remained hemodynamically stable throughout the procedure and his recovery was uncomplicated. He was discharged on the second postprocedural day. At the 6-month follow-up, the patient remained asymptomatic with no evidence of myocardial ischemia. This report informs clinicians of the possibility of burr disconnection and the non-surgical intervention used for its removal.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2024 ","pages":"5482922"},"PeriodicalIF":0.6,"publicationDate":"2024-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11196185/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141447549","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
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
IF 0.6
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
{"title":"Leveraging Color M-Mode to Diagnose Aorto-Atrial Fistula as a Complication of Infective Endocarditis.","authors":"Kramer J Wahlberg, Matthew A Kluge, William E Hopkins","doi":"10.1155/2024/7550403","DOIUrl":"10.1155/2024/7550403","url":null,"abstract":"<p><p>Aorto-atrial fistula is a rare and life-threatening complication of infective endocarditis, classically diagnosed by visualizing a connection between the aorta and atrium with associated continuous flow. A patient presented with bioprosthetic and native valve enterococcal endocarditis with multiple complications, including an aorto-atrial fistula that was diagnosed by color M-mode on transesophageal echocardiography. We review the features of aorto-atrial fistula and utilize this case to demonstrate how M-mode can be leveraged to provide improved temporal resolution in the setting of diagnostic uncertainty.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2024 ","pages":"7550403"},"PeriodicalIF":0.6,"publicationDate":"2024-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11178404/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141332519","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
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。
IF 0.6
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
{"title":"Rare Manifestation of COVID-19 Resulting in Coronary Artery Vasculitis.","authors":"Ahmed Hassaan Qavi, Soban Ahmad, Neeraj N Shah, Rony Shammas","doi":"10.1155/2024/8976833","DOIUrl":"10.1155/2024/8976833","url":null,"abstract":"<p><p>We present the case of a 59-year-old African American female with end-stage renal disease (ESRD) who presented to the emergency department with chest discomfort. She had a coronary angiogram six months ago that showed no occlusive epicardial coronary artery disease. She had elevated troponin I levels and new regional wall motion abnormalities on echocardiogram. Her SARS-CoV-2 returned positive. After a multidisciplinary team approach, she underwent another coronary angiogram that showed new severe multivessel ostial lesions and a left main coronary artery aneurysm. COVID-19-related coronary artery vasculitis was suspected based on her clinical presentation, angiogram findings, and negative autoimmune workup. The patient underwent successful coronary artery bypass grafting and recovered without complications.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2024 ","pages":"8976833"},"PeriodicalIF":0.6,"publicationDate":"2024-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10846917/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139698917","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
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
IF 0.6
Case Reports in Cardiology Pub Date : 2024-01-02 DOI: 10.1155/2024/5596010
Blake Purtle, Jason Wagner, Andrew Zarker, Vishal Patel, David Aguilar
{"title":"Heart Failure in a Young Adult with a Fine-Lubinsky Syndrome: An Unknown Comorbidity","authors":"Blake Purtle, Jason Wagner, Andrew Zarker, Vishal Patel, David Aguilar","doi":"10.1155/2024/5596010","DOIUrl":"https://doi.org/10.1155/2024/5596010","url":null,"abstract":"The Fine-Lubinsky syndrome (FLS) is a rare congenital disorder. Heart failure has not been described in young adults with this condition. Here, we report the first case of heart failure in a young adult patient with FLS. This finding highlights the need for further investigation into cardiac complications in this illness.","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"74 16","pages":""},"PeriodicalIF":0.6,"publicationDate":"2024-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139390639","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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
IF 0.6
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
{"title":"Pacemaker Lead Entanglement during Interventional PFO Occlusion: Salvage Using a Sizing Balloon.","authors":"Andreas Goldschmied, Juergen Schreieck, Michal Droppa","doi":"10.1155/2023/5586197","DOIUrl":"https://doi.org/10.1155/2023/5586197","url":null,"abstract":"<p><p>We present a case of a patient with a transient ischaemic attack (TIA) likely due to paradoxical embolism through a patent foramen ovale (PFO). Her medical history included 2<sup>nd</sup>-degree heart block Mobitz II, which manifested with recurrent syncopes and was treated with a dual chamber pacemaker. During the interventional PFO closure procedure, we noted entrapment of the atrial pacemaker lead between the right-sided occluder disc and the interatrial septum. We were able to successfully move the lead aside using a 24 mm sizing balloon and subsequently developed the right-sided occluder disc in the correct position. In conclusion, pacemaker-lead entrapment between a PFO occluder disc and the interatrial septum can be prevented using a sizing balloon.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"5586197"},"PeriodicalIF":0.6,"publicationDate":"2023-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10733004/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138832877","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
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。
IF 0.6
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":"<p><p>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.</p>","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 <i>Streptococcus gallolyticus</i> 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":"<p><p><i>Background. Streptococcus gallolyticus</i> (previously known as <i>Streptococcus bovis</i> 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. <i>Case Presentation.</i> 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. <i>Conclusions.</i> 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.</p>","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
{"title":"IgG4-Related Pericarditis Diagnosed by Accumulated Pericardial Effusion.","authors":"Hirohito Sugawara, Tomokazu Takahashi, Yukishige Kimura, Azumi Matsui, Tamaki Matsumoto, Kimio Nishisato, Mitsuhiro Nishimura","doi":"10.1155/2023/9223342","DOIUrl":"10.1155/2023/9223342","url":null,"abstract":"<p><p>IgG4-related pericarditis has rarely been reported. Here, we report a case of IgG4-related disease that presented with pericardial effusion. A 67-year-old female who presented with palpitations and chest pain was admitted because of a large amount of pericardial effusion that required drainage. The patient underwent pericardial drainage, and the symptoms were gradually alleviated. IgG4 levels were elevated in the serum and pericardial effusions. A biopsy specimen of <sup>18</sup>F-FDG accumulated in the submandibular gland showed lymphocyte infiltration with IgG4-positive cells. The patient was diagnosed with IgG4-related pericarditis. Glucocorticoids resolved serological and imaging abnormalities. Prompt treatment improves the disease status.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"9223342"},"PeriodicalIF":0.6,"publicationDate":"2023-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10691889/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138479270","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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