Case Reports in Cardiology最新文献

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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。
IF 0.6
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":"<p><p>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.</p>","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
{"title":"To PLEX or Not to PLEX for Amiodarone-Induced Thyrotoxicosis.","authors":"Tania Ahuja, Olivia Nuti, Cameron Kemal, Darren Kang, Eugene Yuriditsky, James M Horowitz, Raymond A Pashun","doi":"10.1155/2023/1563732","DOIUrl":"https://doi.org/10.1155/2023/1563732","url":null,"abstract":"<p><p>Amiodarone-induced thyrotoxicosis (AIT) carries significant cardiovascular morbidity. There are two types of AIT with treatment including antithyroid medications and corticosteroids and treatment of ventricular arrhythmias. Therapeutic plasma exchange (TPE) also known as \"PLEX\" may help remove thyroid hormones and amiodarone. We report a case of PLEX in an attempt to treat cardiogenic shock secondary to AIT. This case highlights the robust rapidly deleterious demise of AIT, specifically in patients with decompensated heart failure. The decision to PLEX or not to PLEX for AIT should be individualized, prior to definitive therapy.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"1563732"},"PeriodicalIF":0.6,"publicationDate":"2023-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10681774/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138464251","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
Proper Treatment and Management of Postcardiotomy Refractory Vasospasm 切开术后难治性血管痉挛的正确治疗和处理
Case Reports in Cardiology Pub Date : 2023-11-10 DOI: 10.1155/2023/9988680
Caleb R. Weissman, Stephane Leung Wai Sang
{"title":"Proper Treatment and Management of Postcardiotomy Refractory Vasospasm","authors":"Caleb R. Weissman, Stephane Leung Wai Sang","doi":"10.1155/2023/9988680","DOIUrl":"https://doi.org/10.1155/2023/9988680","url":null,"abstract":"We present here a unique case in which a 63-year-old man developed diffuse coronary vasospasm on postoperative day (POD) 1 following uneventful aortic valve replacement, replacement of ascending aorta, and coronary artery bypass. Subsequent emergent coronary angiogram demonstrated diffuse native coronary artery vasospasm that was only transiently responsive to intracardiac nitroglycerin, resulting in persistent cardiogenic shock and severe biventricular dysfunction. The patient was, thus, placed on femoral-femoral venoarterial (VA) extracorporeal membrane oxygenation (ECMO) with Impella support. This strategy allowed the weaning of vasopressors and enabled the resolution of the vasospasm. The patient was ultimately discharged on POD 17 without further complications. This case demonstrates our management strategy to provide life-saving support for patients facing postcardiac surgery refractory vasospasm.","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"79 7","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135093233","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
Left Juxtaposition of the Right Atrial Appendage: Pitfalls in Diagnosis 右心耳左并置:诊断中的陷阱
Case Reports in Cardiology Pub Date : 2023-11-09 DOI: 10.1155/2023/1385305
Kanya Singhapakdi, Wesam Sourour, Thomas R. Kimball
{"title":"Left Juxtaposition of the Right Atrial Appendage: Pitfalls in Diagnosis","authors":"Kanya Singhapakdi, Wesam Sourour, Thomas R. Kimball","doi":"10.1155/2023/1385305","DOIUrl":"https://doi.org/10.1155/2023/1385305","url":null,"abstract":"Several congenital anomalies of the right atrial appendage (RAA) have been described including aneurysm, herniation (in association with a pericardial defect), and left juxtaposition. The left juxtaposition of the RAA (LJRAA), first described by Birmingham in 1893 and subsequently introduced by Dixon in 1954, is usually associated with complex cardiac malformations such as obstruction of the left ventricular outflow tract. In this case report, we will describe an unusual variant of LJRAA in the absence of any other cardiac defects, which was initially misinterpreted as an aortic dissection. The correct diagnosis was made after careful reinterpretation and the use of multiple imaging modalities as highlighted.","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":" 7","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135192171","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
Uremic Pericarditis with Cardiac Tamponade in a Patient on Hemodialysis. 血液透析患者尿毒症心包炎合并心包填塞1例。
IF 0.6
Case Reports in Cardiology Pub Date : 2023-11-06 eCollection Date: 2023-01-01 DOI: 10.1155/2023/5099005
Nismat Javed, Marcos Molina, Rabih Nasr, Gilda Diaz-Fuentes
{"title":"Uremic Pericarditis with Cardiac Tamponade in a Patient on Hemodialysis.","authors":"Nismat Javed, Marcos Molina, Rabih Nasr, Gilda Diaz-Fuentes","doi":"10.1155/2023/5099005","DOIUrl":"10.1155/2023/5099005","url":null,"abstract":"<p><p>Uremic pericardial effusion and pericarditis in end-stage kidney disease patients remain one of the causes responsible for high rates of morbidity and occasional mortality. While clinical presentation could be variable, clinicians should have a high index of suspicion for uremic pericarditis especially in patients who miss their dialysis sessions. We present a 77-year-old man with end-stage renal disease on dialysis diagnosed with pericarditis and large pericardial effusion complicated by cardiac tamponade and shock. He underwent urgent pericardiocentesis with clinical improvement. The course of the disease can be complicated by shock with multiorgan failure, particularly the liver. The presentation is relatively acute requiring a high level of suspicion, urgent diagnosis, and management to reduce mortality. As the geriatric population increases with associated comorbid conditions, it would be expected that patients undergoing dialysis would increase. Given the uncommon nature of the disease and how these patients have been managed by multiple specialties and care providers, it is important to consider dialysis-related complications in all patients with end-stage renal disease presenting with dyspnea.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"5099005"},"PeriodicalIF":0.6,"publicationDate":"2023-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643030/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"107592779","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
Nonbacterial Thrombotic Endocarditis of Bioprosthetic Aortic Valve Presenting as Cardioembolic Stroke in a Patient without Predisposing Systemic Disease. 生物瓣膜非细菌性血栓性心内膜炎在无系统性疾病的患者中表现为心源性栓塞性卒中。
IF 0.6
Case Reports in Cardiology Pub Date : 2023-10-12 eCollection Date: 2023-01-01 DOI: 10.1155/2023/5411153
Samuel J White
{"title":"Nonbacterial Thrombotic Endocarditis of Bioprosthetic Aortic Valve Presenting as Cardioembolic Stroke in a Patient without Predisposing Systemic Disease.","authors":"Samuel J White","doi":"10.1155/2023/5411153","DOIUrl":"10.1155/2023/5411153","url":null,"abstract":"<p><p>Nonbacterial thrombotic endocarditis (NBTE) describes a cluster of noninfectious heart valve lesions and is histologically characterised by the presence of sterile platelet and fibrin-rich aggregates. Risk factors include hypercoagulable states such as active malignancy, autoimmune disorders, and prothrombotic haematological conditions. NBTE involving bioprosthetic heart valves is exceedingly rare. We present a case of a 73-year-old man with a bioprosthetic aortic valve and no NBTE risk factors who developed right-sided homonymous hemianopia during an admission for decompensated congestive cardiac failure. After detailed clinical work-up including brain MRI, the man was diagnosed with acute ischemic cardioembolic stroke involving the left posterior cerebral artery territory. He subsequently underwent successful bioprosthetic aortic valve replacement with histologic examination of the explant supporting diagnosis of NBTE. Evidence of new neurological deficit or disturbance in patients with prosthetic heart valves should prompt investigation for cardioembolic stroke. Whilst rare, NBTE should be considered as a differential diagnosis for cardioembolic stroke, even in patients without predisposing systemic disease.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"5411153"},"PeriodicalIF":0.6,"publicationDate":"2023-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586915/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49693795","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
Mitral Valve Echodensities in a Young-Adult Female with Relapsing Polychondritis, Transiently Positive Lupus Anticoagulant, and Systemic Embolism. 一例年轻成年女性复发性多软骨炎、短暂性阳性狼疮抗凝剂和系统性栓塞患者的二尖瓣回声密度。
IF 0.6
Case Reports in Cardiology Pub Date : 2023-10-07 eCollection Date: 2023-01-01 DOI: 10.1155/2023/5073128
Michael C Sauer, Vikram Sharma, Jennifer L M Strouse, Ramzi El Accaoui, Christopher J Benson
{"title":"Mitral Valve Echodensities in a Young-Adult Female with Relapsing Polychondritis, Transiently Positive Lupus Anticoagulant, and Systemic Embolism.","authors":"Michael C Sauer,&nbsp;Vikram Sharma,&nbsp;Jennifer L M Strouse,&nbsp;Ramzi El Accaoui,&nbsp;Christopher J Benson","doi":"10.1155/2023/5073128","DOIUrl":"10.1155/2023/5073128","url":null,"abstract":"<p><strong>Background: </strong>Valvular strands seen on echocardiography carry a wide differential diagnosis and may not always have a clear etiology despite taking clinical context into account. The decision of whether to provide anticoagulation for these lesions can be challenging. <i>Case Presentation</i>. A young adult female with an extensive rheumatologic history involving relapsing polychondritis and positive lupus anticoagulant presents to the emergency department with a discolored and painful right toe, as well as right auricular pain and swelling. Initial work-up revealed a possible splenic infarct, vasculitis of the right lower extremity, and mitral valve echodensities on echocardiography, without evidence of infective endocarditis. Due to concern that nonbacterial thrombotic endocarditis may be the cause of the patient's thromboembolic event, her valvular lesions were treated with low molecular weight heparin while awaiting serial imaging. When follow-up echocardiography showed no change in the size of her mitral valve lesions, which would be most consistent with Lambl's excrescences, the care team still faced a decision about which long-term anticoagulation to prescribe. This patient of childbearing age wished to avoid the teratogenicity and long-term monitoring associated with warfarin therapy. Although warfarin was the preferred agent for the patient's rheumatologic comorbidities, she elected to receive enoxaparin therapy for long-term thromboembolism prophylaxis.</p><p><strong>Conclusions: </strong>Even when accounting for clinical context, valvular lesions seen on echocardiography often have uncertain etiology and may require time and serial imaging to determine which treatment to pursue. When long-term anticoagulation is provided for females of childbearing age, shared decision-making with consideration of the patient's personal priorities and comorbidities is essential.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"5073128"},"PeriodicalIF":0.6,"publicationDate":"2023-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576647/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41240718","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
Cardiac Tuberculoma Presenting as Sudden Cardiac Death in an Immunocompetent Young Man: A Case Report and Literature Review. 免疫功能正常青年心脏结核瘤表现为心源性猝死:病例报告和文献综述。
IF 0.6
Case Reports in Cardiology Pub Date : 2023-10-04 eCollection Date: 2023-01-01 DOI: 10.1155/2023/2207204
Alemayehu Shiferaw Lema
{"title":"Cardiac Tuberculoma Presenting as Sudden Cardiac Death in an Immunocompetent Young Man: A Case Report and Literature Review.","authors":"Alemayehu Shiferaw Lema","doi":"10.1155/2023/2207204","DOIUrl":"10.1155/2023/2207204","url":null,"abstract":"<p><p>Tuberculosis is one of several preventable and curable communicable diseases that is a major cause of morbidity and one of the top ten causes of death worldwide. Cardiac tuberculosis frequently affects the pericardium. Although rare, most cases of tuberculosis involving the myocardium and endocardium present as sudden cardiac death in asymptomatic cases. Information about the myocardial involvement of tuberculosis appears in the literature once in a blue moon. As a result, there is a knowledge gap about cardiac tuberculosis among health professionals. Here, a case of sudden cardiac death from tuberculoma of the right atrium with a secondary thrombus causing bicaval obstruction that is observed in an asymptomatic immunocompetent young man is presented. Furthermore, challenges related to the diagnosis and management of cardiac tuberculosis are discussed, and an overview of the relevant literature is provided to break new ground in early diagnosis and therapy.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"2207204"},"PeriodicalIF":0.6,"publicationDate":"2023-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567508/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41219832","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
Acute Cardiac Manifestations of SARS-CoV-2 Infection: Spotting the Clot. 严重急性呼吸系统综合征冠状病毒2型感染的急性心脏表现:发现凝块。
IF 0.6
Case Reports in Cardiology Pub Date : 2023-09-14 eCollection Date: 2023-01-01 DOI: 10.1155/2023/6366959
Robert N Kerley, Amal John, Sajjad Matiullah, Mark Rogan
{"title":"Acute Cardiac Manifestations of SARS-CoV-2 Infection: Spotting the Clot.","authors":"Robert N Kerley,&nbsp;Amal John,&nbsp;Sajjad Matiullah,&nbsp;Mark Rogan","doi":"10.1155/2023/6366959","DOIUrl":"https://doi.org/10.1155/2023/6366959","url":null,"abstract":"<p><p>A middle-aged gentleman presented with a one-week history of progressive dyspnoea on minimal exertion, persistent haemoptysis, and right calf swelling. His only past medical history of note was a recently positive SARS-CoV-2 nasopharyngeal swab performed as part of a workplace outbreak screening. A CT pulmonary angiogram (CTPA) showed bilateral pulmonary thrombi, extensive consolidation, and a left ventricular (LV) thrombus. A transthoracic echocardiogram (TTE) showed a dilated LV with severely impaired systolic function and LV thrombus. The patient was anticoagulated with warfarin, commenced on IV diuretics and COVID-19 protocol. Cardiac magnetic resonance (CMR) imaging showed a severely dilated nonischaemic cardiomyopathy with a heavy thrombus burden and a fibrosis pattern in keeping with myocarditis. We present a case of COVID-19-related myocardial dysfunction with high thrombotic burden and a discussion of its management.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"6366959"},"PeriodicalIF":0.6,"publicationDate":"2023-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513794/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41157502","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
Kounis and Takotsubo, Two Syndromes Bound by Adrenaline: The "ATAK" Complex. Kounis和Takotsubo,肾上腺素结合的两个综合征:“ATAK”复合体。
IF 0.6
Case Reports in Cardiology Pub Date : 2023-09-14 eCollection Date: 2023-01-01 DOI: 10.1155/2023/7706104
Ravi Vazirani Ballesteros, Juan Carlos Gómez Polo, Carmen Olmos, Isidre Vilacosta
{"title":"Kounis and Takotsubo, Two Syndromes Bound by Adrenaline: The \"ATAK\" Complex.","authors":"Ravi Vazirani Ballesteros,&nbsp;Juan Carlos Gómez Polo,&nbsp;Carmen Olmos,&nbsp;Isidre Vilacosta","doi":"10.1155/2023/7706104","DOIUrl":"https://doi.org/10.1155/2023/7706104","url":null,"abstract":"<p><p><i>Background</i>. The term \"ATAK\" complex has been coined by the association of adrenaline, takotsubo, anaphylaxis and Kounis syndrome. We present an uncommon case of an \"ATAK\" complex with biphasic onset and a midventricular takotsubo pattern. <i>Case Summary</i>. A 50-year-old male was brought to the emergency department in anaphylactic shock. He had progressive exertional dyspnea and angina for the past 2 days. The intravenous administration of adrenaline for anaphylactic shock resulted in chest pain and concerning ECG repolarization findings. The patient was immediately transferred to the catheterization laboratory. Coronary angiography showed a midventricular ballooning pattern without significant coronary stenosis, with subsequent recovery during hospitalization, suggestive of takotsubo syndrome. The allergy tests remained inconclusive for the trigger. <i>Discussion</i>. Adrenaline-mediated stress is the link between these two entities, in which Kounis syndrome itself or anaphylactic shock treatment (adrenaline) are potential triggers for takotsubo syndrome.</p>","PeriodicalId":51760,"journal":{"name":"Case Reports in Cardiology","volume":"2023 ","pages":"7706104"},"PeriodicalIF":0.6,"publicationDate":"2023-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513855/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41163034","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
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